多灶性假性血管内皮瘤累及头皮及鼻子,误诊为肉瘤1例。

IF 1.1 Q4 PATHOLOGY
Neha Mittal, Bharat Rekhi, Priyamvada Singhal, Munita Bal, Swapnil Rane, Asawari Patil, Shivakumar Thiagarajan
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引用次数: 0

摘要

本病例报告旨在报告一个极为罕见的头皮多灶性假肌原性血管内皮瘤(PMHE)的临床病理特征。一名21岁男性在其鼻根和头皮上出现多发局灶性溃疡结节。其中一个皮肤病变是在另一个皮肤科诊所取样的,在那里被诊断为肉瘤。活检切片复查显示界限分明的真皮病变,包括丰满的梭形细胞和上皮样细胞,模仿横纹肌母细胞。免疫组化结果显示,肿瘤细胞AE1/AE3、CD31、fl -1、ERG均呈阳性。i -1被保留。诊断为PMHE。随后,患者接受了大范围切除,术后8个月无症状。PMHE很少报告在头颈部,在那里它可以构成一个诊断陷阱。认识这种肿瘤和适当的免疫组织化学染色是必要的,以及时诊断,以避免根治治疗。对以前记录的类似病例进行了审查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multifocal Pseudomyogenic Hemangioendothelioma Involving the Scalp and Nose, Misdiagnosed as A Sarcoma: A Rare Case Report.

This case report aims to present clinicopathological features of an extremely rare case of multifocal pseudomyogenic hemangioendothelioma (PMHE) in the scalp. A 21-year-old male developed multiple, focally ulcerated, nodules over the root of his nose and scalp. One of the skin lesions was sampled at another dermatology clinic, where this was diagnosed as a sarcoma. A review of biopsy sections showed well-circumscribed dermal lesions, comprising plump spindle and epithelioid cells, mimicking rhabdomyoblasts. Immunohistochemically, tumor cells were positive for AE1/AE3, CD31, FLI-1 and ERG. INI-1 was retained. A diagnosis of PMHE was offered. Subsequently, the patient underwent wide excision and has been asymptomatic for 8 months, post-surgery. PMHE is rarely reported in the head and neck region, where it can constitute a diagnostic pitfall. Awareness of this tumor and appropriate immunohistochemical stains are necessary for its timely diagnosis, in order to avoid radical treatments. A review of similar, previously documented cases is presented.

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来源期刊
CiteScore
1.90
自引率
10.00%
发文量
23
审稿时长
14 weeks
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