Kinné M, Filleron A, Salet R, Saumet L, Baron Joly S, Tran T A
Service de pédiatrie, hôpital Carémeau, CHU de Nîmes, place du Professeur-Robert-Debré, 30029 Nîmes cedex 9, France.
Service de pédiatrie, hôpital Carémeau, CHU de Nîmes, place du Professeur-Robert-Debré, 30029 Nîmes cedex 9, France; Inserm U 1183, équipe 3, groupe nîmois : immuno-régulation et microbiote, faculté de médecine de Montpellier-Nîmes, 186, chemin du Carreau-de-Lanes, CS 83021, 30908 Nîmes cedex 2, France.
Arch Pediatr. 2016 May;23(5):508-13. doi: 10.1016/j.arcped.2016.02.007. Epub 2016 Mar 25.
Sarcoidosis is a systemic granulomatosis disease with a classic triad of presentation: typical clinical and radiological signs, presence of tuberculoid granuloma without caseum in histopathology, and exclusion of other causes of granulomatosis, especially tuberculosis. Sarcoidosis is rare in the general population, and even more so in children. In the literature, few cases of sarcoidosis associated with hypercalcemia have been reported in children. We report here the case of a 14-year-old boy with bone marrow and lymph node sarcoidosis suspected, based on poor general condition with hypercalcemia. The patient was treated with hydration, diuretics, and bisphosphonates with good results. We also performed a literature review of published cases of hypercalcemia since 1990 with a diagnosis of sarcoidosis in children, comparing 23 cases (including ours) on clinical and epidemiological, biological, imaging, and histopathological diagnosis. When hypercalcemia is present in the initial clinical presentation, the diagnosis of sarcoidosis is usually made in younger children. Classical locations of the lesions, including lung, skin, and lymph nodes, were highly suggestive of sarcoidosis. Corticosteroids are commonly used to treat sarcoidosis lesions including hypercalcemia. In conclusion, sarcoidosis in children remains difficult to diagnose because the disease is rare and it is common to have nonspecific symptoms in the clinical picture (with diagnosis delayed between 3 months and several years). The classic triad is not always present. Sarcoidosis should be systematically considered and investigated in case of hypercalcemia of unknown cause in children.
结节病是一种全身性肉芽肿病,具有典型的三联征表现:典型的临床和放射学征象、组织病理学显示存在无干酪样坏死的结核样肉芽肿,以及排除其他肉芽肿病病因,尤其是结核病。结节病在普通人群中较为罕见,在儿童中更是如此。在文献中,儿童结节病合并高钙血症的病例报道较少。我们在此报告一例14岁男孩,因全身状况不佳并伴有高钙血症而疑似患有骨髓和淋巴结结节病。该患者接受了补液、利尿剂和双膦酸盐治疗,效果良好。我们还对1990年以来已发表的儿童结节病合并高钙血症病例进行了文献综述,比较了23例(包括我们的病例)的临床、流行病学、生物学、影像学和组织病理学诊断情况。当初始临床表现出现高钙血症时,结节病的诊断通常在年幼儿童中做出。病变的典型部位,包括肺、皮肤和淋巴结,高度提示结节病。糖皮质激素通常用于治疗包括高钙血症在内的结节病病变。总之,儿童结节病仍然难以诊断,因为该疾病罕见,且临床症状通常不具有特异性(诊断延迟3个月至数年)。典型的三联征并不总是存在。在儿童不明原因高钙血症的情况下,应系统地考虑并调查结节病。