Axillary lesion in a young adult ends up to a peculiar diagnosis: primitive neuro-ectodermal tumor (PNET) of ulnar nerve: a rare case report.

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2024-08-26 eCollection Date: 2024-10-01 DOI:10.1097/MS9.0000000000002505
Mohammadreza Emamhadi, Nooshin Zaresharifi, Zoheir Reihanian, Anita Khalili, Mohammad Taghi Ashoobi, Sama Noroozi Guilandehi, Iraj Baghi, Alireza Mehrvarz
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Abstract

Introduction and importance: Primitive neuro-ectodermal tumor (PNET) is a highly aggressive tumor composed of small round blue cells, mostly developing in children and young adults. Being a member of Ewing's Sarcoma Family of Tumors (ESFT); it has been discussed in two subcategories of central and peripheral PNET. PNETs of peripheral nerves are very uncommon pathologic findings, as to the best of our knowledge only 12 well-documented cases have been yet reported.

Case presentation: A 30-year-old male presented with progressive paresthesia of his right hand's little finger and painless swelling of the right axilla. Magnetic resonance (MR) neurography demonstrated a heterogeneous, high-signal, round mass within the right axilla fossa in proximity to the medial aspect of brachial plexus branches. The clinical and radiological study failed to an accurate diagnosis, thus surgical resection of the tumor was done for tissue evaluation. Histopathologic study of the lesion revealed a neoplasm comprising sheets of small, round, blue cells (Hematoxylin and Eosin stain), which immunohistochemically consisted with the diagnosis of PNET.

Clinical discussion: The differential diagnosis of axillary fossa masses, focusses on peripheral nerve tumors like Schwannoma and PNET. MR neurography aids in evaluation, but tissue diagnosis remains crucial. Treatment involves surgical resection, chemotherapy, and radiotherapy tailored to individual patients.

Conclusion: Although pPNET is not apparently the first differential diagnosis coming to mind when encountering a rapidly growing mass in the axillary fossa with peripheral nerve origin, its highly malignant behavior, makes it crucial to be considered in the differential diagnoses.

一名年轻成年人的腋窝病变最终被确诊为尺骨神经原始神经外胚层肿瘤(PNET):罕见病例报告。
导言和重要性:原始神经外胚层瘤(PNET)是一种由小圆形蓝细胞组成的侵袭性极强的肿瘤,多发于儿童和青壮年。作为尤文肉瘤家族肿瘤(ESFT)的一员,它被分为中枢性和周围性 PNET 两个亚类进行讨论。外周神经的 PNET 是非常罕见的病理结果,据我们所知,目前仅有 12 例记录详实的病例被报道过:一名 30 岁的男性因右手小指进行性麻痹和右侧腋窝无痛性肿胀而就诊。磁共振(MR)神经影像学检查显示,右侧腋窝内靠近臂丛神经分支内侧有一异质、高信号、圆形肿块。临床和放射学检查均未能得出准确诊断,因此对肿瘤进行了手术切除以进行组织评估。病变组织病理学检查显示,肿瘤由成片的小圆形蓝色细胞组成(血红素和伊红染色),免疫组化诊断为 PNET:腋窝肿块的鉴别诊断主要集中在周围神经肿瘤,如许旺瘤和 PNET。磁共振神经显像有助于评估,但组织诊断仍然至关重要。治疗包括手术切除、化疗和放疗,因人而异:虽然当腋窝出现迅速生长的周围神经源性肿块时,pPNET显然不是首先想到的鉴别诊断,但其高度恶性的行为使其成为鉴别诊断中必须考虑的因素。
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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来源期刊
Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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