Scholarly article on topic 'Sarcoidosis in childhood. A rare systemic disease'

Sarcoidosis in childhood. A rare systemic disease Academic research paper on "Clinical medicine"

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{"Childhood sarcoidosis" / "Multiorgan involvement" / Hypercalcemia / "Sarcoidosis infantil" / "Compromiso multiorgánico" / Hipercalcemia}

Abstract of research paper on Clinical medicine, author of scientific article — Antonio Zamora-Chávez, Stanislaw Sadowinski-Pine, Carlos Serrano-Bello, Luis Velázquez-Jones, Omar Josué Saucedo-Ramírez, et al.

Abstract Background Sarcoidosis is a systemic disease of unknown etiology that rarely occurs in children. It usually affects the lungs; however, it may involve various organs. It occasionally affects the general condition, and causes fever, hepatomegaly and splenomegaly. Case report We report the case of a twelve-year-old adolescent with late-onset childhood sarcoidosis which diagnosis was confirmed by lymph node histopathological study. The patient presented general condition, hypercalcemia, erythema nodosum, severe lung disorders, lymphadenopathy, hepatomegaly and testicular mass. He received treatment with steroids, with excellent clinical response. Conclusions We highlight the importance of considering the diagnosis of sarcoidosis in patients with hepatomegaly, lymphadenopathy, diffuse lung damage, erythema nodosum, testicular mass and hypercalcemia, as well as the need for a multidisciplinary approach to assess multiple organ involvement and the early beginning of steroid treatment in order to prevent the progression of the disease.

Academic research paper on topic "Sarcoidosis in childhood. A rare systemic disease"

Bol Med Hosp Infant Mex. 2016;73(2):117-128

Boletín Médico del

Hospital Infantil de México (English Edition)


Sarcoidosis in childhood. A rare systemic disease

Antonio Zamora-Cháveza*, Stanislaw Sadowinski-Pineb, Carlos Serrano-Bellob, Luis Velázquez-Jonesc, Omar Josué Saucedo-Ramírezd, Jonathan Palafox-Florese, Erandi Josefina Mata-Vázqueza

a Internal Medicine Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico b Pathology Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico c Nephrology Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico d Allergy and Immunology Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico e Pneumology Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico

Received 20 November 2015; accepted: 17 February 2016 Available online 8 April 2016


Childhood sarcoidosis; Multiorgan involvement; Hypercalcemia


Background: Sarcoidosis is a systemic disease of unknown etiology that rarely occurs in children. It usually affects the lungs; however, it may involve various organs. It occasionally affects the general condition, and causes fever, hepatomegaly and splenomegaly.

Case report: We report the case of a twelve-year-old adolescent with late-onset childhood sarcoidosis which diagnosis was confirmed by lymph node histopathological study. The patient presented general condition, hypercalcemia, erythema nodosum, severe lung disorders, lym-phadenopathy, hepatomegaly and testicular mass. He received treatment with steroids, with excellent clinical response.

Conclusions: We highlight the importance of considering the diagnosis of sarcoidosis in patients with hepatomegaly, lymphadenopathy, diffuse lung damage, erythema nodosum, testicular mass and hypercalcemia, as well as the need for a multidisciplinary approach to assess multiple organ involvement and the early beginning of steroid treatment in order to prevent the progression of the disease.

© 2016 Hospital Infantil de México Federico Gómez. Published by Masson Doyma México S.A.This is an open access article under the CC BY-NC-ND license ( by-nc-nd/4.0/).

☆ Please cite this article as: Zamora-Chávez A, et al. Sarcoidosis en la infancia. Una rara enfermedad sistémica. Bol Med Hosp Infant Mex. 2016;73:117-28.

* Corresponding author. E-mail: (A. Zamora-Chávez).

2444-3409/© 2016 Hospital Infantil de México Federico Gómez. Published by Masson Doyma México S.A. This is an open access article under the CC BY-NC-ND license (

Sarcoidosis en la infancia. Una rara enfermedad sistémica Resumen

Introducción. La sarcoidosis es una enfermedad sistémica de etiología desconocida que raramente se presenta en la infancia. Generalmente afecta los pulmones; sin embargo, puede involucrar diversos órganos. Ocasionalmente afecta el estado general, y origina fiebre, hepatome-galia y esplenomegalia.

Caso clínico. Se presenta el caso de un adolescente de doce años de edad con sarcoidosis infantil de inicio tardío, cuyo diagnóstico fue confirmado con un estudio histopatológico de ganglio linfático. El paciente cursó con afección general, hypercalcemia, eritema nodoso, alteraciones pulmonares graves, adenopatías, hepatomegalia y masa testicular. Recibió tratamiento con es-teroides, con excelente respuesta clínica.

Conclusiones. Se resalta la importancia de considerar el diagnóstico de sarcoidosis en los pacientes con hepatomegalia, adenopatías, daño pulmonar difuso, eritema nodoso, masa testicular e hypercalcemia, así como la necesidad del abordaje multidisciplinario para valorar el compromiso orgánico múltiple y el inicio oportuno de la terapia con esteroides, con el fin de evitar la progresión de la enfermedad.

© 2016 Hospital Infantil de México Federico Gómez. Publicado por Masson Doyma México S.A. Este es un artículo Open Access bajo la licencia CC BY-NC-ND ( licenses/by-nc-nd/4.0/).


Sarcoidosis infantil; Compromiso multiorgánico; Hipercalcemia

1. Introduction

Sarcoidosis is a chronic systemic disease of unknown etiology and worldwide distribution which is usually diagnosed in adults. Sarcoidosis in childhood is very rare.

Lungs are the most frequently affected organs; however, the disease can involve other organs such as eyes, skin, lymph nodes and joints. Less often it involves the nervous system, heart and urogenital tract, causing nephrolithiasis and a testicular mass; in some cases, fever of unknown origin with splenomegaly and hepatomegaly are observed.

The diagnosis of sarcoidosis is made by exclusion of other diseases. Therefore, once there is clinical suspicion, a biopsy of the organs involved shows, as a characteristic histopathological finding, the presence of noncaseating epithelioid granulomas.1

The first descriptions of sarcoidosis were made in Europe in the late nineteenth century. In 1877, in England, J. Hutchinson studied a patient with chronic skin lesions, arthritis and chronic renal failure, and named the skin findings papillary psoriasis. In France, in 1889, E. Besnier also described the skin lesions and named them lupus pernio. In 1899, in Denmark, C. Boeck labeled the skin histological lesions with the term sarkoid because of its similarity with sarcoma. In 1914, in Sweden, N. J. Schaumann described the systemic presentation of the disease; likewise, he pointed out that both Besnier's lupus pernio and Boeck's sarkoid were manifestations of the same disease, as the tissues affected in these patients showed granulomas which he called benign lymphogranulomatosis to differentiate them from Hodgkin's malignant granuloma. The neurologic involvement in sarcoidosis was reported by C. Heerfordt in 1923 who described patients with uveo-pa-rotid fever and lesion of cranial nerves.

The acute pulmonary form of sarcoidosis accompanied of mediastinal lymphadenopathy and erythema nodosum,

arthritis and uveitis was described in Sweden in 1953 by S. Lofgren.

For more than 130 years, most of the studies on sarcoidosis have been performed in adults. However, pediatric cases have been reported since 1923. The condition was known as Besnier-Boeck-Schaumann disease until 1958 when the Sarcoidosis World Congress was carried out in London and the term sarcoidosis was generalized.2 3

Nowadays, accordingly to the international consensus established by the American Thoracic Society, the European Respiratory Society and the World Association for Sarcoidosis and Other Granulomatosis, sarcoidosis is considered to be a systemic granulomatous disease of unknown etiology, which usually affects adults, and is very rare in children.45

The incidence and severity of sarcoidosis vary in different regions of the world and in different ethnic groups probably due to variations in environmental exposures, the prevalence of HLA alleles and other genetic factors. Scandinavia, England, the United States and Japan have the highest prevalence of the disease; in Sweden, the morbidity rate in the general population is 64/100,000 and in the United States, 35/100,000.

There are very few epidemiological data on children. The rate of morbidity of childhood sarcoidosis is 0.29/100,000; however, this rate varies from 0.06/100,000 in children under 4 years to up to 1.02/100,000 in adolescents aged 14 to 15 years.6-8

Regarding mortality from sarcoidosis, during the period 1999-2010 the National Center for Health Statistics reported sarcoidosis as a cause of death in 10,348 of 29,176,040 deaths which represents a rate of 2.8/1,000,000 inhabitants. However, mortality in the African-American population was 12 times higher than in Caucasian population.9

In Mexico, the incidence of sarcoidosis is low, probably due to genetic factors or underreporting of cases. There-

fore, there are no studies on the epidemiology of childhood sarcoidosis since only thirteen cases have been published in the last 20 years, including the case of a teenager with lung disease published by the National Institute of Respiratory Diseases and another report from the National Institute of Pediatrics about two cases of early-onset cutaneous sarcoidosis.10-12

Sarcoidosis is a chronic inflammatory disease that results from the action of an environmental agent that triggers an initial immune response of T-helper cells type 1(Th1) and leads to the development of noncaseating granulomas with systemic involvement in genetically susceptible individuals.

According to epidemiological findings of the multicenter ACCESS (A Case Control Etiologic Study of Sarcoidosis), some environmental conditions are associated with an increased risk for developing sarcoidosis, generating anti-genic stimuli, which act as a trigger of the process. Some of the environmental conditions studied are organic materials (ragweed, pine leaves and seeds), inorganic materials (silica, beryllium, zirconium, titanium, aluminum and fiberglass) and microorganisms (Mycobacterium tuberculosis, Propionibacterium acnes, Brucella, Borrelia, Leptospira, Mycoplasma, Leishmania and Schistosoma).

Although an infectious agent has not been conclusively identified (by culture or by ribosomal RNA markers in tissue from biopsies), the hypothesis of a microbiological agent is the most accepted because there is clinical and epidemiological evidence of transmissibility of sarcoidosis. This observation comes from transplant patients who have developed the disease after tissue or organ transplantation from donors with sarcoidosis. Besides, it has been reported the development of sarcoidosis in the transplanted lung of a patient suffering from the disease; moreover, animals implanted with tissue from affected patients develop granu-lomas.13-18

The existence of a predisposing genetic factor explains the higher incidence of the disease in relatives of patients with sarcoidosis, as well as differences in the prevalence and clinical course of the disease in different ethnic groups.

Recent research with molecular biology techniques has shown that genetic alterations associated with sarcoidosis are located in the major histocompatibility complex (MHC), on the short arm of chromosome 6, in histocompatibility antigens HLA I, such as HLA-B7 and HLA-B8, as well as in alleles of HLA class II such as HLA-DR5, HLA-DR6, HLA-DR8 and HLA-DR9, which are related to high risk in Asian population. Likewise, genetic alterations are found in HLA -DRB1 in the African American population. In European population, HLA-DR14 and HLA-DR15 are related to chronic sarcoidosis, HLA-DR3 with the acute form, and HLA-DR17 with self-limited presentations of sarcoidosis.

The immune mechanisms that cause sarcoidosis are not completely known but it is assumed that macrophages do not adequately recognize and present antigens to T lymphocytes. However, patients with sarcoidosis do not have other evident manifestation of a cellular or humoral immunodeficiency.

The process begins when the antigen phagocyted by the macrophage and the dendritic cell are presented on

the MHC site. This enables the T cell to locate and bind to the MHC-II complex, and consequently to be activated and have clonal expansion, demonstrated by the increase in T cell receptor (TCR) mRNA, and by the presence of markers of antigen-specific T cell activation, such as CD69, glycoprotein 240 and the very late antigen-1 (VLA-1).

Afterwards, T-CD4 lymphocytes differentiate to a Th-Iphenotype, and release cytokines such as interferon-Y (IFN-y), tumor necrosis factor-a (TNF-a), transforming growth factor-B (TGF-B), IL-1B, IL-2, IL-12, IL-15 and IL-18, as well as several chemokines such as macrophage inflammatory protein 3a (MIP3a), interferon-inducible protein-10 (IP-10), monocyte chemotactic protein-1 (MCP-1) and CCL5 or RANTES (regulated on activation, normal T cell expressed and secreted). These chemokines maintain cell recruitment at sites of granuloma formation by their chemotactic effect.

T-regulatory cells from patients with chronic active sar-coidosis have altered function which leads to the persistence of inflammatory process and progression of granulomas. By contrast, patients with Lofgren syndrome, which is a form of acute sarcoidosis with a high rate of remission, have increased T-regulatory cells which reduce lymphocyte proliferation and cytokine production.

In some patients, the initial Th1-type response is replaced by a predominantly T-helper cell type 2 (Th2) response, characterized by a decrease in IFN-y, persistence of TNF-aand TGF-B activities, production of angiotensin converting enzyme (ACE), neopterin and IL-8. These proteins reduce the formation of granulomas but, on the other hand, lead to the development of fibrosis due to the activity of some macrophage cytokines, like type1-insulin growth factor (IGF-1), platelet growth factor, IL-4 and IL-13 which generate fibroblast activation and collagen and fi-bronectin deposition in the extracellular space. The cause of progression to this fibro-proliferative form is unclear, but it may involve the loss of apoptotic mechanisms, loss of regulatory response, or persistence of an antigen that cannot be recognized or properly processed, which causes fibrous scarring and repair of the affected tissue with chronic and irreversible damage.19-24

Vitamin D deficiency has been shown to lead to an increased risk of sarcoidosis, as the antigen presenting cells (macrophages, monocytes and dendritic cells) have vitamin D receptors. This vitamin inhibits macrophage activation induced by IFN-y and decreases the macrophage MHC II antigen presenting activity; so, it is supposed that this deficiency leads to altered regulation of Th1 cells, allowing a persistent immune response.25-27

Furthermore, it has been found that activated macrophages are capable of producing active vitamin D3 (cal-citriol or 1,25-dihydroxycholecalciferol) and parathyroid hormone related peptide (PTHrP), which could contribute to hypercalcemia and hypercalciuria frequently present in this condition.28 29

One of the most remarkable findings in sarcoidosis is an immunological paradox. This paradox is characterized by intense cellular immune response in the affected organs in contrast to a situation of peripheral immunological aner-gy, observed as a lack of response to PPD and other intradermal tests. The likely explanation for this phenomenon is the presence of lymphopenia in peripheral blood, and

especially to the activity of suppressor T CD8+ lymphocytes.

Another phenomenon which is also subject of interest and controversy is the formation of granulomas in the skin of patients with sarcoidosis four to six weeks after the application of sarcoid tissue extract in the Kveim-Siltz-bachtest (used in the past for diagnostic purpose).3031

The histological finding characteristic of sarcoidosis is the presence of noncaseating epithelioid granulomas diffusely scattered in different tissues that mainly affect lymph nodes.

The granulomas of sarcoidosis have compact appearance with well-defined borders. They may be at different stages of development, ranging from highly cellular granulomas to structures of decreased cellularity with fibrosis or progressive hyalinization; besides, they do not have central necrosis neither foreign bodies, in contrast to granulomas caused by mycobacterial and fungal infections, or infestations by systemic metazoans.

The typical sarcoidosis granuloma has two characteristic zones described below:

1. The central zone or follicle is a dense cluster of epithelioid cells, accompanied by lymphocytes, macrophages, Langhans multinucleated giant cells, mast cells and fibroblasts. In 60% of the cases, star shaped structures (asteroid bodies) and lamellar PAS+ structures of 1-15 microns in diameter called Schaumann bodies can be observed. Immunohistochemical staining shows that the central zone of an active granuloma has macrophages in various stages of activation and differentiation. This zone is surrounded by CD4+ T cells intercalated with a small number of CD8+ T cells and B cells.

2. The peripheral zone is formed by a ring of lymphocytes, monocytes and fibroblasts. T-regulatory CD3+/ CD4+/CD25+/Foxp3+ cells accumulate in this outer zone in addition to CD8+ T cells and fibroblasts, which leads to fibrosis when granulomas activity decreases.

In the chronic form of the disease, granulomas may be encapsulated by a fibrous halo or may be replaced by scars of fibrous and hyaline tissue.32-34

The clinical presentation of sarcoidosis in children varies as it depends on the extent of the disease and the organs involved. In most cases of childhood sarcoidosis, multiple organs are affected with a diffuse inflammatory reaction that causes systemic symptoms such as fever, fatigue, hyporexia, nausea and weight loss, in addition to the specific signs and symptoms arising from dysfunction of each affected organ.

Sarcoidosis in childhood can occur in two clinical forms:

1. Early onset sarcoidosis or Blau syndrome: It occurs before age five sporadically or in a familiar cluster. It is associated with NOD2/CARD15 gene located on chromosome 16. In 75 % percent, the cases present a clinical triad characterized by polyarthritis, uveitis and rash, whereas the remaining 25% are accompanied by other organs signs.

2. Late onset sarcoidosis: It develops in children older than 5 years and resembles the adult clinical form. It is

not associated with mutations in the NOD2/CARD15 gene and it is characterized by fever, multiorgan involvement, especially lung, skin, nervous system, eyes, kidneys, joints, lymph nodes, liver and spleen.35-36

The lung is involved in over 90% of cases; however, the clinical spectrum of the disease is wide. Most cases occur in an acute form, with malaise and non-specific respiratory symptoms such as dry cough, dyspnea and airway hy-perresponsiveness, but the disease can start insidiously and with minimal symptoms. The condition is mainly located in the pulmonary interstitium, with enlarged hilar, tracheobronchial and mediastinal lymph nodes.

Approximately 70% of cases resolve spontaneously, but the remaining 30% evolves to chronicity and cause irreversible changes in lung parenchyma with fibrosis and formation of pneumatoceles that lead to chronic respiratory failure and death.

Spirometry and plethysmography show a restrictive pattern, coincident with pulmonary dysfunction, and are useful to assess disease progression and response to treatment.

Sarcoidosis may be stratified in four radiographic stages, which guide the clinician to choose the treatment plan and to make a prognosis. In addition, radiographic imaging allows the follow up of the disease; the probability of remission decreases according to the stage of evolution of the lesions. This is, while radiographic resolution in the first three stages of the disease is feasible, during stage IV, which is considered the end stage, radiographic lesions are already irreversible37 (Table 1).

The incidence of ocular involvement varies from 30 to 70%. The characteristic lesion is uveitis. However, conjunctiva, sclera, crystalline and lacrimal glands may also be affected, resulting in cataract, glaucoma and dry keratoconjunctivitis. In the posterior segment patients may develop vitritis, ischemic retinal vasculitis with neovascu-larization, occlusion of the central retinal vein, optic nerve affection, macular edema, perforating lesions, "wax drops" exudates and retinal detachment with blindness, which can be detected by slit lamp eye examination and retinangiog-raphy.38 39

Skin disorders occur in 20 to 30% of the patients. The most frequent lesion is erythema nodosum, used as a marker of acute sarcoidosis since it usually disappears in 6-8 weeks. The simultaneous appearance of erythema nodosum, fever, joint pain and hilar lymphadenopathy is

Table 1 Chest radiographic staging*

Stages Findings Remission

Stage 0 Normal chest radiograph > 90%

Stage I Bilateral hilar lymphadenopathy 60-90%

Stage II BHL plus pulmonary infiltrations 40-60°%

Stage III Pulmonary infiltrations without 10-20%

Stage IV Pulmonary fibrosis 0%

'Adaptation from The American Thoracic Society Statement on

Sarcoidosis (ref. 4).

called Lofgren syndrome. Other skin lesions include subcutaneous nodules, psoriasis like plaques, alopecia, hyper-pigmented lesions and leukocytoclastic vasculitis.

Joint involvement is present in 80% of cases. It can be in the form of migratory polyarthritis and/or persistent arthritis, as well as granulomatous tenosynovitis. When polyarthritis, rash and uveitis occur in children under 5 years, it is recognized as Blau syndrome.40

Nervous system involvement occurs in 10% of patients, usually with involvement of II and VII cranial nerves as a result of granulomatous meningitis. However, CNS involvement is found in up to 25% of autopsy cases of sarcoidosis.

Cardiac involvement is diagnosed clinically in less than 5% of patients with sarcoidosis, although it has been found that 20 to 30% of post-mortem studies have lesions in the conduction system, which can cause arrhythmias and sudden death. Echocardiographic findings include ventricular dysfunction and decreased ejection fraction of the left ventricle; however, histological evidence of myocardial biopsies requires cardiac catheterization.

Exocrine glands are frequently affected. Sarcoidosis can involve parotid and minor salivary glands in up to 60% of cases; granulomatous pancreatitis has also been reported.

Renal involvement occurs in 10% of patients due to hypercalcemia, nephrocalcinosis and nephrolithiasis.

Clinical genitourinary involvement has been reported in

0.2. of cases, and in 5% of autopsy studies, the most frequent alteration being scrotal mass.41"48-

The diagnosis of childhood sarcoidosis is performed with the same criteria established for adults, published by the American Thoracic Society and the European Respiratory Society in 1999:

1. Compatible clinical scenario.

2. Histological evidence of noncaseating granulomas in biopsies obtained from the affected organs.

3. Exclusion of other pathological processes that may present with a similar clinical or histopathological presentation, especially mycobacterial and fungal infections and other immunological processes.

There is no definitive test available to confirm the diagnosis of sarcoidosis. However, auxiliary studies are:

1. Cytological analysis of bronchoalveolar lavage of patients with sarcoidosis shows a predominant lymphocyte cellularity in > 90% of cases. Furthermore, a CD4/ CD8 ratio > 3.5 by flow cytometry, has sensitivity of 52-59% and specificity of 94-96% for the diagnosis of sarcoidosis.49-51

2. Kveim-Siltzbach test has been used for sarcoidosis diagnosis since 1941. It consists of an intradermal inoculation of a suspension obtained from spleen tissue of patients with sarcoidosis; a skin biopsy should be per-

formed 6 weeks after inoculation in search of granulomas. The test has sensitivity of 75% and specificity > 90%, but currently its clinical application is restricted because of the difficulty in obtaining the reagent; besides, it requires that the patient has not received steroids, and some authors have discouraged it because of the risk of transmission of infectious diseases.51,52

3. Serum angiotensin converting enzyme (ACE) quantification has been used in the diagnosis of the disease, because 80% of pediatric patients with sarcoidosis have elevated ACE. It is also useful as a marker of disease activity as the enzyme levels descend when patients are in remission.

4. Measurement of soluble receptor of interleukin-2 (sIL-2R) is a test that has been very useful in evaluating the activity of the sarcoidosis.53-55

5. Serum and urinary calcium are both useful in the diagnosis and monitoring of disease progression, as hyper-calcemia occurs in 20% of cases and hypercalciuria in up to 60% and depend on the activity and the extent of the disease.56-60

2. Clinical case

We present the case of a twelve-year-old male with no relevant family history, parents and four siblings healthy. He was the product of a first pregnancy, born at term by vaginal delivery without perinatal complications. He had achieved age-appropriate psychomotor development and had a complete immunization schedule. He had no medical history except for chickenpox at the age of 6 years without complications.

Symptomatic disease began one year earlier with his first visit to the hospital, presenting dry cough in isolated bouts. During the last 6 months he had loss 12 kg of weight, and had asthenia, hyporexia, paleness, nausea and occasional vomiting of gastric content. Four months earlier, a mass growing in the left supraclavicular region and painless subcutaneous nodules appeared on both forearms. A week before admission he attended a regional hospital because of abdominal colic pain in the right flank and tenderness to lumbar percussion. Abdominal ultrasound showed hepatomegaly and right nephrolithia-sis, so he was referred to our institution.

On physical examination, the pacient was conscious and well oriented, emaciated, pale, with equal sized pupils reactive to light, without abnormal findings in ear, nose or throat. Cranial nerves function was preserved. The neck showed no jugular engorgement; he had cervical nodes of 0.5 to 1 cm, and a 2 cm mobile, painless node was present in the left supraclavicular zone which had no erythema or temperature increase. He had tachypnea and light intercostal retraction, respiratory movements were normal and breath sounds were normal without rales or wheezing. Heart sounds were rhythmic and without murmurs. The abdomen was soft. Hepatic border was 6 cm and spleen border 4 cm below the costal edge, bowel sounds were normal. He had Tanner II genital development stage and an asymmetric scrotum. Left testicle had a painless increase of volume with no transillumination. Extremities were hypotrophic with erythema nodosum located in forearms and legs, had symmetrical peripheral pulses, normal tendon reflexes with no pyramidal signs.

Initial laboratory test results were: hemoglobin 14.4 g/ dl, leukocytes 7,600/mm3, neutrophils 48%, band forms 4%, lymphocytes 37%, monocytes 7% platelets 286,000/ mm3, erythrocyte sedimentation rate 38 mm/h. C-reactive

protein <0.319 mg/dl. Blood chemistry showed glucose 91 mg/dl, creatinine 1.5 mg/dl, BUN 17 mg/dl, uric acid 6 mg/ dl, serum proteins 8.6 g/dl, albumin 3.2 g/dl, globulins 5.4 g/dl, total bilirubin 0.36 mg/dl, direct bilirubin 0.9 mg/dl, indirect bilirubin 0.27 mg/dl, ALT 35 U, AST 26 U, cholesterol 120 mg/dl, triglycerides 160 mg/dl, Na 129 mmol/l, K 3.6 mmol/l, Cl 98 mmol/l, Ca 13 mg/dl, P 4.02 mg/dl, Mg 2.4 mg/dl, serum osmolality 268 mOsm/l. ABG without oxygen: pH 7.43, pCO2 32.4 mmHg, pO249.9 mmHg, HCO3 21.3 mmol/l, SO2 83%, lactate 2.4 mmol/l, anion Gap 13.6 mmol/l, TP 12.4'', TTP 29.3''.

Serologic studies for hepatitis A, B and C, CMV, EBV, varicella zoster, and type I and II herpes simplex virus were negative. ELISA for HIV was negative. Anti-ds-DNA antibodies, antinuclear antibodies (ANA), anti-neutrophil-cytoplasmic antibodies (p-ANCA and c-ANCA) and VDRL were negative.

The urinalysis reported a density of 1.020, pH 6.0, abundant erythrocytes, leukocytes 1-2/field, negative nitrites, protein 75 mg/dl, sediment with calcium oxalate crystals and amorphous phosphate.

Twenty four-hour urine collection showed a creatinine clearance of 70.4 mg/ml/min, calciuria of 10.9 mg/kg/day, phosphaturia of 63.1 mg/kg/day. Tubular phosphate reabsorption was 63.3%, phosphorus/creatinine ratio (P/cr) 0.80 mg/mg and calcium/creatinine ratio (Ca/cr) was 0.52 mg/mg. Twenty four-hour oxaluria was 53.7 mg (<38 mg) and 24-h citric acid urine excretion, 427 mg (100-1300 mg).

Serum cystatin C, 2.18 mg/l (0.53-0.95 mg/l), parathyroid hormone (PTH), <1.20 pg/ml (10-55 pg/ml), calcitriol (1, 25-dihydroxy-vitamin D), 30.7 pg/ml (19.9-79.3 pg/ml), angiotensin converting enzyme (ACE), 272 U/l (13-100 U/l). Alphafetoprotein, 1.07 ng/ml (<10 ng/ml), human chorionic gonadotropin, 1.20 mIU/ml (<5 mIU/l).

PPD test with candidin control was negative. BAAR search in three samples of gastric juice was negative.

Bone marrow aspirate showed decreased cellularity, diminished megakaryocytes, metamyelocytes 2.5%, band forms 10.5%, mature neutrophils 35%, eosinophils 3%, lymphocytes 23.5%, blasts 1.5%, and normoblasts 24%.

Serum immunoglobulins: IgA 724 mg/dl (108-325 mg/dl), IgE 82.6 mg/dl (0-100 mg/dl), IgM 175 mg/dl (70-150 mg/ dl), IgG 2710 mg/dl (770-1510 mg/dl).

Complement: C3 113 mg/dl (90-180 mg/dl), C4 16.6 mg/ dl (10-40 mg/dl).

Nitroblue tetrazolium slide test and chemiluminescence at rest and after stimulus were normal. Soluble Interleu-kin-2 receptor (sIL-2R), 3230 U/ml (406 -1100 U/ml).

Flow cytometry showed a normal quantity of T and B lymphocytes with a CD4/CD8 ratio of 1.22 (Table 2).

The initial chest X-ray showed diffuse reticular and mi-cronodular infiltrates with bilateral hilar lymphadenopa-thy (Figure 1).

X-rays showed normal skull, and long bones with evidence of decalcification (Figure 2).

Thoracoabdominal computed tomography showed lymph node clusters in the mediastinum, mesentery, retroperito-neal and inguinal regions, bilateral diffuse micronodular infiltration of the lungs, hepatomegaly, splenomegaly, and right renal calculi (Figure 3).

Renal ultrasound reported normal sized kidneys with regular morphology, appropriate corticomedullary rela-

Table 2 Peripheral blood flow cytometry.

Lymphocyte subpopulation

Cells % N

Lymph events - 2,501

Bead events - 1,528

CD3+ 50.7 790.84

CD3+CD8+ 22.15 345.52

CD3+CD4+ 27.03 421.62

CD3+CD4+CD8+ 1.28 19.96

CD16+CD56+ 13.71 213.93

CD19+ 33.47 522.03

CD45+ - 1,559.85

CD4/CD8 ratio 1.22

Figure 1 Bilateral hilar lymphadenopathy and micronodular and diffuse reticular infiltrates.

Figure 2 Osteopenia and bone demineralization.

tionship with no dilatation of collecting systems. The right kidney had a stone of 6.7 mm located at the sinus. Doppler perfusion image was normal.

Testicular ultrasound showed both testes and right epididymis of normal size, whereas the left epididymis was

Figure 3 Retroperitoneal lymphadenopathy and right kidney stones.

enlarged, lobed and with well-defined borders, a size of 15x7x15 mm and central vascularity on Doppler mode (Figure 4).

Eye fundoscopy showed temporal and inferior-nasal periphlebitis which are vascular changes characteristic of sarcoidosis (Figure 5). However, fluorescein angiography reported a 3/10 excavation in both eyes, central emergency of vessels, attached retinas, and normal choroidal phase without alterations in vascular pathways (Figure 6).

Echocardiogram showed an anatomically normal heart, left ventricle ejection fraction 72%, shortening fraction 40%, right ventricle systolic pressure 17 mmHg, diastolic interventricular septum 9 mm.

Pulmonary function test results (quality grade A, met ATS acceptability and repeatability criteria). Spirometry:

FEV, / FVC 89 (102), FVC 2.73 (91%), FEV1 2.43 (93%). Plethysmography: SVC 2.72 (90), IC 1.85 (74), ERV 0.87 (164), TGV 1.27 (71), RV 0.40 (45), TLC 3.11 (73) RV/TLC 13 (57), compatible with a mild restrictive pattern.

Supraclavicular lymph node biopsy. Hematoxylin-eosin, Grocott, Ziehl-Neelsen and PAS staining were performed. Histological sections showed loss of lymph node architecture, secondary to the formation of multiple confluent noncaseating granulomas (Figure 7), made of numerous epithelioid macrophages, giant Langhans cells and other cells of foreign body-type. Concentric calcifications or Schaumann bodies were observed occasionally (Figure 8) as well as asteroid bodies (Figure 9). Neither special stains nor PCR nor cultures identified Mycobacterium tuberculosis. Histopathological diagnosis: supraclavicular lymph nodes with chronic noncaseating granulomatous lymphadenitis compatible with sarcoidosis.

In the early days of hospital stay, the patient had headache and Kernig and Brudzinski signs. Cranial computed tomography showed adequate differentiation of gray and white matter, normal ventricular system and vascular structures without meningeal alterations. Cerebrospinal fluid (CSF) was transparent, proteins 30 mg/dl, glucose 49 mg/dl, leukocytes 1 /field. Gram stain and cultures were negative. PCR test for Mycobacterium tuberculosis in CSF was negative.

Treatment was initiated with prednisone 2 mg/kg/day and hydrochlorothiazide 1.2 mg/kg/day. The patient showed clinical improvement in his general condition, remission of hepatomegaly and splenomegaly, erythema no-dosum, as well as disappearance of lymphadenopathy and the testicular mass. Mediastinal lymph nodes and pulmonary infiltrates also disappeared (Figure 10).

Figure 5 Fundoscopy: temporal and inferior nasal periphlebitis.

Figure 6 Retinal fluorangiography: normal vessels.

Figure 7 Lymph node biopsy with non-caseating granulomas.

Figure 8 Lymph node biopsy with Schaumann bodies.

Figure 9 Lymph node biopsy with asteroid bodies.

Figure 10 Lymphadenopathy and pulmonary infiltrates remission after treatment.

Four months later, the patient was asymptomatic, had recovered 15 kg of weight and had resumed school. In follow up, abdominal tomography showed remission of retro-peritoneal lymphadenopathy and no evidence of renal calculi; spirometry and plethysmography had a normal pattern. Laboratory tests showed serum calcium 9.0 mg/ dl, phosphorus 5.8 mg/dl, creatinine 0.8 mg/dl, uric acid 6.2 mg/dl, 24-hour calciuria 0.93 mg/kg/day, and ACE was 71 U/l. According to these values, it was considered that the sarcoidosis was in remission.

3. Discussion

This case is about an adolescent male with late-onset pediatric sarcoidosis who had serious affection of the general state leading to cachexia. He also had lung damage, hepatomegaly, splenomegaly, adenopathy, erythema no-dosum and a scrotal mass. The diagnostic approach to patients with hepatosplenomegaly, allowed to rule out several infectious diseases such as tuberculosis, systemic mycosis, syphilis, Epstein Barr virus (EBV) and human immunodeficiency virus (HIV), as well as infiltrative disorders, such as leukemias, lymphomas, metastatic tumors and hemophagocytic lymphohistiocytosis by computed tomography, and bone marrow and lymph node biopsies. Systemic vasculitis and other autoimmune diseases were discarded as well as testicular tumors based on the findings of testicular ultrasound and normal levels of the tumor markers alpha-fetoprotein and beta-gonadotrophin.61

The diagnosis of sarcoidosis was suspected because of the presence of a systemic disease with hypercalcemia, hypercalciuria and urolithiasis, accompanied by elevated levels of ACE and sIL-2R. It was confirmed by histopatho-logical study of a lymph node which showed the presence of multiple noncaseating epithelioid granulomas formed by macrophages, giant Langhans cells, asteroid bodies and Schaumann bodies. Cytological analysis of bronchoalveolar lavage and the Kveim-Siltzbach test could not be performed.

On admission, the patient had chronic respiratory failure type I (hypoxemia, normocarbia and hyperlactatemia) with no cardiovascular repercussion. Chest radiography showed diffuse reticular and micronodular infiltrates with bilateral hilar lymphadenopathy concordant with the stage II of the American Thoracic Society for thoracic sarcoidosis classification. Likewise, spirometry and plethysmography reported a decrease in FEV1/FVC, compatible with mild restrictive lung disease as described in the first two stages of pulmonary sarcoidosis, and which normalized after prednisone treatment.

During his hospital stay, the patient also presented headache and meningeal signs which we attributed to sar-coidosis infiltration of the meninges, since CSF cytochemi-cal and microbiological studies were normal as well as cranial computed tomography. These clinical findings also disappeared after prednisone administration.62 63

Although the patient never had ocular manifestations, ophthalmological examination was carried out due to the high frequency of ocular involvement in sarcoidosis. Periphlebitis was compatible with uveal sarcoidosis. As previously described, this is the treatment of choice since

sarcoidosis eye injuries usually improve rapidly after prednisone administration, preventing disease progression and the appearance of other irreversible damage which may lead to blindness.64

Hypercalcemia of sarcoidosis traditionally has been attributed to calcitriol production by activated macrophages and monocytes from granulomas, which in turn increase the intestinal absorption of calcium and osteoclast activity with bone resorption and increased levels of serum calcium. However, in this case, the determination of calcitriol (1, 25-dihydroxy-vitamin D3) was found to be within the reference interval, and suppressed PTH levels; this is indicative of inhibition of the parathyroid glands due to elevated serum calcium and, on the other hand, hypercalcemia was probably caused by another autonomous factor such as PTHrP production by activated macrophages, which could not be measured in this case.65

Initially the patient had acute renal failure, but no renal replacement therapy was needed. Hypercalcemic hypercalciuria with decreased tubular phosphate reabsorption, which was expressed as calcium oxalate and calcium phosphate, caused him kidney stones. While the acute colic pain is uncommon in children with urolithiasis, this patient presented right flank pain accompanied by microscopic hematuria. As part of the medical management, treatment with hydrochlorothiazide was provided in order to reduce the renal calcium excretion and decrease the formation of calcium oxalate and calcium phosphate calculi, achieving remission of hypercalciuria and expulsion of renal calculi (Figure 11).66-72

In this patient no studies of histocompatibility antigens (HLA) were performed. Regarding immune function, moderate polyclonal hypergammaglobulinemia was observed, with appropriate levels of C3 and C4, as described in patients with sarcoidosis. The phagocytic function tests ni-troblue tetrazolium slide test and chemiluminescence at rest and after stimulus were normal, so the possibility of chronic granulomatous disease was discarded.

While flow cytometry on peripheral blood reported a total number of lymphocytes within the normal interval,

Figure 11 Abdominal computed tomography after treatment: retroperitoneal lymphadenopathy remission and kidney stone disappearance.

the identification of the major lymphocyte subpopulations showed 50.7% of T cells, 33.4% of B lymphocytes and 13.7% of NK cells with one CD4/CD8 ratio = 1.22. This could explain the immune paradox observed in skin tests because it was considered that the patient had normal cellular and humoral immunity.73"77

Finally, it should be noted that childhood sarcoidosis is an underdiagnosed disease in Mexico, so there is no clinical or epidemiological information about this condition in our population. This clinical case may contribute to the knowledge of sarcoidosis in children whose clinical symptoms are nonspecific. In the few reported cases, sarcoido-sis has been misdiagnosed as juvenile idiopathic arthritis, tuberculosis or systemic fungal infections. However, the involvement of multiple organs may lead to serious disability and/or death, highlighting the importance to consider sarcoidosis in the diagnostic approach of patients with generalized lymphadenopathy, splenomegaly and hepatomegaly in order to initiate glucocorticoid therapy, which is the most effective treatment to prevent disease and stop its progression in most of these patients.

Ethical disclosure

Protection of human and animal subjects. The authors declare that no experiments were performed on humans or animals for this study.

Confidentiality of data. The authors declare that no patient data appear in this article.

Right to privacy and informed consent. The authors declare that no patient data appear in this article.

Conflict of interest

The authors declare no conflict of interest of any nature.


1. Fauroux B, Clément A. Sarcoidosis. In: Taussig LM, Landau LI, editors. Pediatric respiratory medicine. Philadelphia: Mosby-Elsevier Inc; 2008. pp. 717-23.

2. Sharma OP. Definition and history of sarcoidosis. Eur Respir Mon. 2005;32:1-12.

3. Sharma OP. Sarcoidosis: a historical perspective. Clin Dermatol. 2007;25:232-41.

4. Statement on sarcoidosis. Joint Statement of the American Thoracic Society (ATS), the European Respiratory Society (ERS) and the World Association of Sarcoidosis and Other Granulomatous Disorders (WASOG) adopted by the ATS Board of Directors and by the ERS Executive Committee, February 1999. Am J Respir Crit Care Med. 1999;160:736-55.

5. Shetty AK, Gedalia A. Sarcoidosis in children. Curr Probl Pediatr. 2000;30:149-76.

6. Rybicki BA, Major M, Popovich J Jr, Maliarik MJ, Iannuzzi MC. Racial differences in sarcoidosis incidence: a 5-year study in a health maintenance organization. Am J Epidemiol. 1997;145:234-41.

7. Hoffmann AL, Milman N, Byg KE. Childhood sarcoidosis in Denmark 1979-1994: incidence, clinical features and laboratory

results at presentation in 48 children. Acta Paediatr. 2004;93:30-6.

8. ACCESS Research Group. Design of A Case Control Etiologic Study of Sarcoidosis (ACCESS). J Clin Epidemiol. 1999;52:1173-86. doi: 10.1016/S0895-4356(99)00142-0.

9. Mirsaeidi M, Machado RF, Schraufnagel D, Sweiss NJ, Baughman RP. Racial difference in sarcoidosis mortality in the United States. Chest. 2015;147:438-49.

10. Carrillo-Pérez DL, Apodaca-Chávez EI, Carrillo-Maravilla E, Mejía-Ávila M, Hernández-Oropeza JL, Reyes E, et al. Sarcoidosis: a single hospital-based study in a 24-year period. Rev Invest Clin. 2015;67:33-8.

11. Julián-González RE, Saez-de-Ocariz M, Orozco-Covarrubias L, Durán-McKinster C, Ruiz-Maldonado R. Sarcoidosis de inicio temprano. Rastreo de casos nuevos en pacientes previamente diagnosticados con artritis idiopática juvenil. Dermatol Pediatr Latinoam. 2012;10:58-63.

12. Cruz AID, Barón LS, Garrido GC, Velázquez SJR. Sarcoidosis infantil. Una rara enfermedad pediátrica. Caso clínico. Rev Chil Pediatr. 2011;82:535-41.

13. Shetty AK, Gedalia A. Childhood sarcoidosis: a rare but fascinating disorder. Pediatr Rheumatol Online J. 2008;6:16. doi: 10.1186/1546-0096-6-16

14. Mitchell DN, Rees RJ. A transmissible agent from sarcoid tissue. Lancet. 1969;2:81-4.

15. Padilla ML, Schilero GJ, Teirstein AS. Donor-acquired sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis. 2002;19:18-24.

16. Müller C, BriegelJ, Haller M, Vogelmeier C, Bittman I, Welz A, et al. Sarcoidosis recurrence following lung transplantation. Transplantation. 1996;61:1117-9.

17. Ikonomopoulos JA, Gorgoulis VG, Kastrinakis NG, Galanos AA, Karameris A, Kittas C. Experimental inoculation of laboratory animals with samples collected from sarcoidal patients and molecular diagnosis evaluation of the results. In Vivo. 2000;14:761-5.

18. Rotsinger JE, Drake WP. Sarcoidosis: unknown etiology and genetic predisposition provides therapeutic challenges. J Pulm Respir Med. 2014;4:190. doi: 10.4172/2161-105X. 1000190.

19. du Bois RM, Beirne PA, Anevlavis SE. Genetics of sarcoidosis. Eur Respir Mon. 2005;32:64-81.

20. Iannuzzi MC, Iyengar SK, Gray-McGuire C, Elston RC, Baughman RP, Donohue JF, et al. Genetic-wide search for sarcoidosis susceptibility genes in African Americans. Genes Immun. 2005;6:509-18.

21. Rybicki BA, Hirst K, IyengarSK, Barnard JG, Judson MA, Rose CS, et al. A sarcoidosis genetic linkage consortium: the Sarcoidosis Genetic Analysis (SAGA) study. Sarcoidosis Vasc Diffuse Lung Dis. 2005;22:115-22.

22. Gerke AK, Hunninghake G. The immunology of sarcoidosis. Clin Chest Med. 2008;29:379-90.

23. Agostini C, Cassatella M, Zambello R, Trentin L, Gasperini S, Perin A, et al. Involvement of the IP-10 chemokine in sarcoid granulomatous reactions. J Immunol. 1998;161:6413-20.

24. Nureki SI, Miyazaki E, Ando M, Ueno T, Fukami T, Kumamoto T, et al. Circulating levels of both Th1 and Th2 chemokines are elevated in patients with sarcoidosis. Respir Med. 2008;102:239-47. doi: 10.1016/j.rmed.2007.09.006.

25. Baughman RP, Teirstein AS, Judson MA, Rossman MD, Yeager H, Bresnitz EA, et al; Case Control Etiologic Study of Sarcoidosis (ACCESS) research group. Clinical characteristics of patients in a case control study of sarcoidosis. Am J Respir Crit Care Med. 2001;164(10 Pt 1):1885-9.

26. Mihailovic-Vucinic V, Ignjatovic S, Dudvarski-Ilic A, Stjepanovic M, Vukovic M, Omcikus M, et al. The role of vitamin D in multisystem sarcoidosis. J Med Biochem. 2012;31:339-46.

27. Hagaman JT, Panos RJ, McCormack FX, Thakar CV, Wikenheiser-Brokamp KA, Shipley RT, et al. Vitamin D deficiency and

reduced lung function in connective tissue-associated interstitial lung diseases. Chest. 2011;139:353-60.

28. Hayes CE, Nashold FE, Spach KM, Pedersen LB. The immunological functions of the vitamin D endocrine system. Cell Mol Biol (Noisy-le-grand). 2003;49:277-300.

29. Krikorian A, Shah S, Wasman J. Parathyroid hormone-related protein: an unusual mechanism for hypercalcemia in sarcoidosis. Endocr Pract. 2011;17:e84-e86.

30. Miyara M, Amoura Z, Parizot C, Badoual C, Dorgham K, Trad S, et al. The immune paradox of sarcoidosis and regulatory T cells. J Exp Med. 2006;203:359-70.

31. Siltzbach LE. The Kveim test in sarcoidosis. A study of 750 patients. JAMA. 1961;178:476-82. doi:10.1001/jama.1961. 03040440028006.

32. Newman LS, Rose CS, Maier LA. Sarcoidosis. N Engl J Med. 1997;336:1224-34.

33. DeRemee RA. Sarcoidosis. Mayo Clin Proc. 1995;70:177-81.

34. Pritchard J, Foley P, Wong H. Langerhans and Langhans: what's misleading in a name? Lancet. 2003;362:922.

35. Rosé CD, Wouters C. Pediatric Sarcoidosis. In: Petty RE, Laxer RM, Lindsley CB, Wedderburn LR, editors. Textbook of pediatric rheumatology. Philadelphia: Elsevier, Inc; 2016. pp. 517-525.

36. Rosé CD, Doyle TM, McIlvain-Simpson G, Coffman JE, Rosenbaum JT, Davey MP, et al. Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis. J Rheumatol. 2005;32:373-5.

37. Milman N, Hoffmann AL. Childhood sarcoidosis: long-term follow-up. Eur Respir J. 2008;31:592-8.

38. Rothova A, Suttorp-van Schulten MS, Frits Treffers W, Kijlstra A. Causes and frequency of blindness in patients with intraocular inflammatory disease. Br J Ophthalmol. 1996;80: 332-6.

39. Altan-Yaycioglu R, Akova YA, Akca S, Yilmaz G. Inflammation of the posterior uvea: findings on fundus fluorescein and indocyanine green angiography. Ocul Immuno Inflamm. 2006;14:171-9.

40. Rosé CD, Aróstegui JI, Martin TM, Espada G, Scalzi L, Yagüe J, et al. NOD2-associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain. Arthritis Rheum. 2009;60:1797-803. doi: 10.1002/art.24533.

41. Lazarus A. Sarcoidosis: epidemiology, etiology, pathogenesis, and genetics. Dis Mon. 2009;55:649-60.

42. Lindsley CB, Petty RE. Overview and report on international registry of sarcoid arthritis in childhood. Curr Rheumatol Rep. 2000;2:343-8.

43. Ricker W, Clark M. Sarcoidosis; a clinicopathologic review of 300 cases, including 22 autopsies. Am J Clin Pathol. 1949;19:725-49.

44. Massarweh NN, Bhalani VK, Shaw KK, Crawford B, Lang E, Davis R. Testicular presentation of sarcoidosis and organ preservation: case report and review of management strategies. Urology. 2006;67:200.

45. Turk CO, Schacht M, Ross L. Diagnosis and management of testicular sarcoidosis. J Urol. 1986;135:380-1.

46. Reinkes EZ, MacLennan GT. Sarcoidosis of the testis and epididymis. J Urol. 2008;179:1147. doi: 10.1016/j.juro.2007. 12.012

47. Rabinovich CE, Fels E, Shanahan J, Majure JM, Murphy TM. Sarcoidosis. Pulmonary Manifestations of Rheumatoid Diseases. In: Turcios NL, Fink RJ, editors. Pulmonary manifestations of pediatric diseases. Philadelphia: Saunders-Elsevier Inc; 2009. pp. 201-240. doi: 10.1016/B978-1-4160-3031-7.00010-3

48. Rosé CD, Wouters CH, Meiorin S, Doyle TM, Davey MP, Rosenbaum JT, et al. Pediatric granulomatous arthritis: an international registry. Arthritis Rheum. 2006;54:3337-44.

49. Thomeer M, Demedts M. Predicitive value of CD4/CD8 ratio in bronchoalveolar lavage in the diagnosis of sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis. 1997;14(Suppl 1):36.

50. Welker L, Jorres RA, Costabel U, Magnussen H. Predictive value of BAL cell differentials in the diagnosis of interstitial lung diseases. Eur Respir J. 2004;24:1000-6.

51. Wigley RD. Moratorium on Kveim test. Lancet. 1993;341:1284.

52. Marcoval J, Graells J, Mañá J, Baumann E, Moreno A, Peyrí J. Current value of the Kveim test in the diagnosis of sarcoidosis. Actas Dermosifiliogr. 2003;94:642-5.

53. Grutters JC, Fellrath JM, Mulder L, Janssen R, van den Bosh JM, van Velzen-Blad H. Serum soluble interleukin-2 receptor measurement in patients with sarcoidosis: a clinical evaluation. Chest. 2003;124:186-95.

54. Bargagli E, Bianchi N, Margollicci M, Olivieri C, Luddi A, Coviello G, et al. Chitotriosidase and soluble IL-2 receptor: comparison of two markers of sarcoidosis severity. Scand J Clin Lab Invest. 2008;68:479-83.

55. Létorneau S, Krieg C, Pantaleo G, Boyman O. IL-2- and CD25-dependent immunoregulatory mechanisms in the homeostasis of T-cell subsets. J Allergy Clin Immunol. 2009;123:758-62.

56. Bachiller-Corral J. Otras Causas de Hipercalcemia. In: Sociedad Española de Reumatología. Manual de enfermedades óseas. Madrid: Editorial Médica Panamericana, S. A. 2010: pp. 143-148.

57. Conron M, Young C, Beynon HLC. Calcium metabolism in sarcoidosis and its clinical implications. Rheumatology. 2000;39:707-13.

58. González-Lamuño D. Hipercalciuria. Pediatr Integral. 2013;17:422-32.

59. Schwartz GJ, Haycock GB, Edelmann CM Jr, Spitzer A. A simple estimate of glomerular filtration rate in children derived from body length and plasma creatinine. Pediatrics. 1976;58: 259-63.

60. Guignard JP, Santos F. Laboratory Investigations. In: Avner ED, Harmon WE, Niaudet P, editors. Pediatric Nephrology. Philadelphia: Lippincott Williams & Wilkins; 2004. pp. 399-424.

61. Caballero-Mora FJ, Muñoz-Calvo MT, García-Ros M, Rodríguez de Alarcón J, Fernández-Pérez ML, Casco F, et al. Tumores testiculares y paratesticulares en la infancia y adolescencia. An Pediatr. 2013;78:6-13.

62. Weil RJ. Meningeal neurosarcoidosis mimicking convexy meningioma. Case illustration. J Neurosurg. 2001;94:1013.

63. Zajicek JP, Scolding NJ, Foster O, Rovaris M, Evanson J, Moseley IF, et al. Central nervous system sarcoidosis-diagnosis and management. Q J Med. 1999;92:103-17.

64. Díaz-Valle D, Méndez R, Arriola P, Cuiña R, Ariño M. Enfermedades sistémicas no infecciosas y uveítis. An Sist Sanit Navar. 2008;31(Supl. 3):97-110.

65. Lim V, Clarke BL. Coexisting primary hyperparathyroidism and sarcoidosis cause increased angiotensin-converting enzyme and decreased parathyroid hormone and phosphate levels. J Clin Endocrinol Metab. 2013;98:1939-45.

66. Ammenti A, Pelizzoni A, Cecconi M, Molinari PP, Montini G. Nephrocalcinosis in children: a retrospective multi-centre study. Acta Paediatr. 2009;98:1628-31.

67. Milliner DS, Murphy ME. Urolithiasis in pediatric patients. Mayo Clin Proc. 1993;68:241-8.

68. Stapleton FB, Roy S 3rd, Noe HN, Jerkins G. Hypercalciuria in children with hematuria. N Engl J Med. 1984;310:1345-8.

69. Voghenzi A, Bezzi TM, Luscardi P, Soriani S. Acquired hyperoxaluria and haematuria in children. Pediat Nephrol. 1992;6:356-7.

70. Fernández-Rodríguez A, Arrabal-Martín M, García-Ruiz MJ, Arrabal-Polo MA, Pichardo-Pichardo S, Zuluaga-Gómez A. Papel de las tiazidas en la profilaxis de la litiasis cálcica recidivante. Actas Urol Esp. 2006;30:305-9.

71. Preminger GM, Pak CY. Eventual attenuation of hypercalciuric response to hydrochlorothiazide in absorptive hypercalciuria. J Urol. 1987;137:1104-9.

72. Türk C, Knoll T, Petrik A, Sarica K, Seitz C, Straub M, et al. Guía clínica sobre la urolitiasis. European Association of Urology. 2010. Available from:

73. Segal BH, Holland SM. Primary phagocytic disorders of childhood. Pediatr Clin North Am. 2000;47:1311-38.

74. Barrera-Ramírez LM, Drago SME, Pérez RJ, Zamora AC, Gómez AF, Sainz ETR, et al. Citometría de flujo: vínculo entre la

investigación básica y la aplicación clínica. Rev Inst Nal Enf Resp Mex. 2004;17:42-55.

75. Ramírez-Vargas NG, Berrón-Ruiz LR, Berrón-Pérez R, Blancas-Galicia L. Diagnóstico de enfermedad granulomatosa crónica; pacientes y portadoras. Rev Alergia Mex. 2011;58:120-5.

76. Holland SM. Chronic granulomatous disease. Clin Rev Allergy Immunol. 2010;38:3-10.

77. Silva MT. When two is better than one: macrophages and neutrophils work in concert in innate immunity as complementary and cooperative partners of a myeloid phagocyte system. J Leukoc Biol. 2010;87:93-106.