小儿结节病误诊为肝脾脓肿:一例报告和复习。

IF 2.2 Q3 RHEUMATOLOGY Journal of Rheumatic Diseases Pub Date : 2022-07-01 DOI:10.4078/jrd.2022.29.3.181
Su Min Lee, Hyungwook Choi, Sungmin Lim, Jehee Shin, Ji-Man Kang, Jong Gyun Ahn
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引用次数: 1

摘要

结节病是一种病因不明的系统性肉芽肿性疾病,以肉芽肿形成为特征。由于结节病在儿童患者中的发病率有限,对这种疾病的临床病程知之甚少。临床、放射学和病理学检查的结合是必要的,以排除其他鉴别诊断(即感染和肉芽肿性炎症性疾病)并确定结节病的诊断。在这里,我们报告了一例组织学证实的结节病,最初被误诊为肝脾脓肿,发生在一名11岁男性身上。皮质类固醇治疗改善了他的症状,并解决了他的皮肤和肝脾损伤。三年的后续行动波澜不惊。本研究强调了在存在肉芽肿组织学证据的情况下,考虑儿童多器官受累结节病的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Pediatric Sarcoidosis Misdiagnosed as Hepatosplenic Abscesses: A Case Report and Review.

Sarcoidosis is a systemic granulomatous disorder of unknown etiology characterized by granuloma formation. Due to the limited incidence of sarcoidosis in pediatric patients, little is known about the clinical course of this disease. A combination of clinical, radiologic, and pathologic examination is necessary to exclude other differential diagnoses (i.e., infection and granulomatous inflammatory disorder) and establish a diagnosis of sarcoidosis. Here, we report a case of histologically confirmed sarcoidosis initially misdiagnosed as hepatosplenic abscesses in an 11-year-old male. Treatment with corticosteroids improved his symptoms and resolved his skin and hepatosplenic lesions. A three-year follow-up was uneventful. This study emphasizes the importance of considering sarcoidosis in children presenting with findings of multi-organ involvement in the presence of histologic evidence of granuloma.

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CiteScore
2.30
自引率
5.00%
发文量
39
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