Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL, USA.
Pediatr Rheumatol Online J. 2012 Aug 31;10(1):32. doi: 10.1186/1546-0096-10-32.
We report a now 6-year-old African-American male with both Alagille syndrome and pediatric sarcoidosis. With a prior JAG1 mutation positive diagnosis of Alagille syndrome, he presented to the hospital with a subacute, predominantly respiratory febrile condition, eventually diagnosed as sarcoidosis. A liver biopsy revealed paucity of bile ducts and scattered epithelioid granulomas, while a skin biopsy showed granulomatous angiitis, a manifestation of sarcoidosis not yet reported in a pediatric patient. He has subsequently been treated with corticosteroids, mycophenolate mofetil, and infliximab with clinical response. Alagille syndrome and sarcoidosis have not yet been reported in the medical literature in the same patient to the best of our knowledge. We briefly review these two seemingly unrelated conditions and propose a possible common pathogenic mechanism.
我们报告了一例现 6 岁的非裔美国男性,患有 Alagille 综合征和儿童期结节病。该患者曾因 JAG1 突变阳性诊断为 Alagille 综合征,因亚急性、主要为呼吸道发热就诊,最终诊断为结节病。肝脏活检显示胆管稀少和散在的上皮样肉芽肿,而皮肤活检显示肉芽肿性血管炎,这是一种在儿科患者中尚未报道的结节病表现。此后,他接受了皮质类固醇、霉酚酸酯和英夫利昔单抗治疗,临床反应良好。据我们所知,Alagille 综合征和结节病在同一患者中的医学文献中尚未被报道。我们简要回顾了这两种看似不相关的疾病,并提出了一种可能的共同发病机制。