Mlika Mona, Hamrouni Rim, Zeddini Abdelfatteh, Braham Emna, Ismail Olfa, El Mezni Faouzi
Tunis Med. 2015 Jul;93(7):427-9.
Histiocytic sarcoma (HS) is a rare hematologic malignancy with morphologic and immunophenotypic evidence of histiocytic differentiation. This tumor follows an aggressive clinical course.
We report the case of a 14 year-old white girl who presented with a nodular lesion in the thigh, involving the skin and soft tissue. The histologic diagnosis retained was a HS.
HS is a rare neoplasm that may cause a diagnostic pitfall. Unfortunately, incomplete clinical data and histopathologic disparities in addition to the overall rarity of the neoplasms induced difficulties of management and of full appreciation of their clinical behavior.
组织细胞肉瘤(HS)是一种罕见的血液系统恶性肿瘤,具有组织细胞分化的形态学和免疫表型证据。该肿瘤临床进程侵袭性强。
我们报告一例14岁白人女孩,其大腿出现一个结节性病变,累及皮肤和软组织。最终组织学诊断为HS。
HS是一种罕见肿瘤,可能导致诊断陷阱。不幸的是,除了肿瘤总体罕见外,临床数据不完整和组织病理学差异导致管理困难以及难以全面了解其临床行为。