耳廓孤立性浅表血管黏液瘤:诊断难题及文献复习。

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Archive of clinical cases Pub Date : 2023-09-26 eCollection Date: 2023-01-01 DOI:10.22551/2023.40.1003.10258
Anurag Singh, Shalini Rawat, Gulshan Kumar, Uma Shankar Singh, Mala Sagar
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引用次数: 0

摘要

浅表性血管黏液瘤是一种极为罕见的皮下黏液样软组织肿瘤。由于这种肿瘤的罕见性,很少有细针抽吸细胞学和组织病理学结果的病例报告。在这里,我们描述了一例浅表性血管黏液瘤,发生在一名24岁女孩身上,她在出现时或在手术切除肿瘤后的两年随访结束时,有一个没有卡尼综合征的孤立左耳耳廓肿块。浅表血管黏液瘤的临床、细胞形态学和组织学表现,以及免疫组织化学标志物,在英国文献中首次在这一罕见病例报告中进行了描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Solitary superficial angiomyxoma of the ear pinna: a diagnostic dilemma with a review of literature.

Solitary superficial angiomyxoma of the ear pinna: a diagnostic dilemma with a review of literature.

Solitary superficial angiomyxoma of the ear pinna: a diagnostic dilemma with a review of literature.

Solitary superficial angiomyxoma of the ear pinna: a diagnostic dilemma with a review of literature.

Superficial angiomyxoma is an extremely rare subcutaneously placed myxoid soft tissue neoplasm. There are few case reports with fine needle aspiration cytological and histopathological findings available for this tumor because of its rarity. Here, we describe a case of superficial angiomyxoma in a 24-year-old girl who had a solitary left ear pinna mass without a Carney's complex at the time of presentation or at the end of two years of follow-up next to the surgical removal of the tumor. The clinical, cytomorphological, and histological findings, together with the immunohistochemical markers, in a case of superficial angiomyxoma are described in this rare case report for the first time in the English literature.

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