肢端纤维软骨粘液样瘤表现为扩大结节累及远端指尖及颏下:1例报告。

IF 0.9 Q4 DERMATOLOGY Case Reports in Dermatology Pub Date : 2023-03-16 eCollection Date: 2023-01-01 DOI:10.1159/000529568
Rhiannon C Miller, Cynthia M Magro, Laura E Melnick, Shari R Lipner
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引用次数: 0

摘要

肢端纤维软骨粘液样瘤是一种新发现的良性软组织肿瘤,表现为手指或脚趾的单一结节性病变。以前只有一篇关于这种肿瘤的报道,一个病例系列描述了最初的病理和临床表现;然而,临床病史、体格检查和结果的细节尚不清楚。在这个报告中,我们描述了一个39岁的男性谁提出了一个痛苦的扩大肿块累及远端右手第三指和颏下部。行穿刺活检,显微镜检查发现病变为肢端纤维软骨粘液样瘤。x线片未见骨骼受累。肿瘤成功切除,疼痛症状完全缓解。我们讨论的临床特点和免疫组织化学发现我们的情况下,目前有限的知识对这种非常罕见的肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Acral Fibrochondromyxoid Tumor Presenting as Enlarging Nodule Involving the Distal Fingertip and Hyponychium: A Case Report.

An acral fibrochondromyxoid tumor is a newly described type of benign soft tissue neoplasm that presents as a single nodular lesion on a finger or toe. There has only been one previous report on this tumor, a case series that described the initial pathologic and clinical findings; however, details on clinical history, physical examination, and outcome are unknown. In this report, we describe a case of a 39-year-old male who presented with a painful enlarging mass involving the distal right 3rd finger and hyponychium. Punch biopsy was performed and the lesion was identified as an acral fibrochondromyxoid tumor on microscopic examination. X-ray showed no bony involvement. The tumor was successfully excised with complete resolution of pain symptoms. We discuss the clinical features and immunohistochemistry findings of our case in the context of the current limited knowledge about this very rare tumor.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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