A rare case of hemophagocytic lymphohistiocytosis associated with sarcoidosis

V. Marwah, N. Kumar, R. Choudhary, D. Mutreja, Anmol Sharma
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Abstract

Sarcoidosis is a chronic granulomatous disorder often misdiagnosed as tuberculosis. Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal complication linked to extensive hemophagocytosis and hyperinflammatory response. Cases of sarcoidosis developing HLH are rarely documented and difficult to diagnose. We present the case of a 63-year-old female with sarcoidosis complicated with HLH, successfully managed at our center.
嗜血球性淋巴组织细胞增多症合并结节病一例
结节病是一种慢性肉芽肿性疾病,常被误诊为肺结核。噬血细胞性淋巴组织细胞增多症(HLH)是一种潜在的致命并发症,与广泛的噬血细胞增多和高炎症反应有关。结节病发展为HLH的病例很少有记录,而且很难诊断。我们报告一例63岁女性结节病合并HLH,在我们中心成功治疗。
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