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婴儿肌纤维瘤病:细针穿刺活检提示诊断

Infantile myofibromatosis: diagnosis suggested by fine-needle aspiration biopsy.

作者信息

Ostrowski M L, Bradshaw J, Garrison D

机构信息

Department of Pathology, University Hospital of Jacksonville, FL 32209.

出版信息

Diagn Cytopathol. 1990;6(4):284-8. doi: 10.1002/dc.2840060412.

Abstract

A newborn male infant presented with multiple subcutaneous and parenchymal lesions. These lesions, thought clinically to represent disseminated neuroblastoma, were assessed via fine-needle aspiration biopsy. The spindled cells and associated collagen were interpreted as a type of fibromatosis, most probably infantile myofibromatosis. This diagnosis was subsequently confirmed histologically, and the patient experienced spontaneous involution or regression of all lesions by 18 mo of age. To our knowledge, this is the first documented case of this entity initially suggested on the basis of a fine-needle aspiration biopsy specimen.

摘要

一名男婴出生时即出现多处皮下和实质病变。临床认为这些病变代表播散性神经母细胞瘤,遂通过细针穿刺活检进行评估。梭形细胞及相关胶原被诊断为一种纤维瘤病,很可能是婴儿肌纤维瘤病。这一诊断随后经组织学证实,该患儿在18个月大时所有病变均出现自发退化或消退。据我们所知,这是首例基于细针穿刺活检标本初步诊断该病的记录病例。

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