Isolated splenic sarcoidosis: A case report.

IF 0.6
Coro Velasco Gametxogoikoetxea, Irene Fernández De Los Reyes, Fermín Jiménez Bermejo
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引用次数: 0

Abstract

Isolated splenic sarcoidosis is a rare entity, but clinicians should consider it in patients with compatible clinical features. Its diagnosis is challenging due to the broad differential diagnosis, which includes hematologic and splenic neoplasms, infiltrative and inflammatory disorders, autoimmune diseases, and infections. We report the case of a 15-year-old female diagnosed with isolated splenic sarcoidosis during hospitalization for fever of unknown origin. Histopathological examination revealed non-caseating granulomas and necrotizing granulomas. The patient showed marked clinical and radiological improvement following corticosteroid therapy, supporting the diagnosis. Despite its atypical presentation, this case highlights the importance of including sarcoidosis in the diagnostic evaluation of prolonged fever, even in young patients without respiratory symptoms.

孤立性脾结节病1例。
孤立性脾结节病是一个罕见的实体,但临床医生应考虑它在患者的相容临床特征。由于其广泛的鉴别诊断,包括血液学和脾肿瘤、浸润性和炎症性疾病、自身免疫性疾病和感染,其诊断具有挑战性。我们报告一个15岁的女性病例诊断为孤立性脾结节病住院期间发烧不明原因。组织病理学检查显示非干酪化肉芽肿和坏死性肉芽肿。患者在皮质类固醇治疗后表现出明显的临床和影像学改善,支持诊断。尽管其表现不典型,但该病例强调了将结节病包括在长时间发烧的诊断评估中的重要性,即使在没有呼吸道症状的年轻患者中也是如此。
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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