全身性爆发性组织细胞增多症诊断的临床病理相关性

Sandhya Chauhan, Anchana Gulati, G. Tegta, M. Gupta
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引用次数: 0

摘要

组织细胞增多症是一种罕见的疾病,由单核吞噬细胞和免疫调节效应系统的反应性或恶性增殖引起。全身性爆发性组织细胞增多症(GEH)是一种罕见的组织细胞增多症,由Winkelmann和Muller首先描述[1]。迄今为止,只有大约43例GEH报告。[2]我们报告一位41岁男性,怀疑为汉森病,但临床病理相关证实为GEH。
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Clinicopathological correlation in diagnosis of generalized eruptive histiocytosis
Sir, Histiocytoses are a rare group of disorders resulting from reactive or malignant proliferation of mononuclear phagocyte and immunoregulatory effector system. Generalized eruptive histiocytosis (GEH) is a rare variant of histiocytosis first described by Winkelmann and Muller.[1] There are only approximately 43 case reports of GEH till date.[2] We are reporting a 41-year-old male who was suspected as Hansen’s disease, but clinicopathological correlation confirmed GEH.
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