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局限于蝶鞍的伴有巨大淋巴结病的窦性组织细胞增生症。

Sinus histiocytosis with massive lymphadenopathy localized to the sella.

作者信息

Ng H K, Poon W S

机构信息

Department of Anatomical & Cellular Pathology, Prince of Wales Hospital, Chinese University of Hong Kong.

出版信息

Br J Neurosurg. 1995;9(4):551-5. doi: 10.1080/02688699550041223.

Abstract

Sinus histiocytosis with massive lymphadenopathy (SHML) is a condition of unknown aetiology characterized by proliferation of histiocytes and lymphocytes, with the former phagocytosing the latter producing a typical histological appearance. Although first described in lymph nodes, cases have been reported in many extranodal sites, including the central nervous system. We report a case of SHML involving the sella turcica producing diabetes inspidus and pituitary dysfunction.

摘要

伴有巨大淋巴结病的窦性组织细胞增生症(SHML)是一种病因不明的疾病,其特征为组织细胞和淋巴细胞增生,前者吞噬后者,产生典型的组织学表现。尽管最初在淋巴结中被描述,但在包括中枢神经系统在内的许多结外部位都有病例报道。我们报告一例累及蝶鞍的SHML病例,该病例导致尿崩症和垂体功能障碍。

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