Malignant Para-Testicular Mesothelioma: A Rare Presentation in the Tunica Vaginalis of an Elderly Male With No Prior Asbestos Exposure.

IF 0.9 4区 医学 Q4 PATHOLOGY International Journal of Surgical Pathology Pub Date : 2024-09-01 Epub Date: 2024-01-02 DOI:10.1177/10668969231215426
Nada Shaker, Heath Blankenship, Nuha Shaker, Ruwaida Ben Musa, Shuo Niu, Alaaeddin Alrohaibani, Ibrahim Mansoor, Rafat Abu Shakra, Omar P Sangueza
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Abstract

Malignant mesothelioma of the tunica vaginalis is an extremely rare and aggressive tumor that is frequently encountered in elderly patients. The diagnosis of malignant mesothelioma of the tunica vaginalis poses a diagnostic challenge due to its infrequency and nonspecific clinical presentation. Histopathological examination and immunohistochemical staining are essential in differentiating this tumor from other para-testicular masses and establishing a definitive diagnosis. Early detection and comprehensive treatment planning are crucial for improving the prognosis and overall outcomes for patients with this rare malignancy. We present a report of malignant mesothelioma of the tunica vaginalis in a 78-year-old male patient with no history of asbestos exposure who presented with a large infiltrative left para-testicular mass. Histopathological examination revealed a biphasic proliferation composed of epithelioid and spindle cells with infiltrative features, foci of necrosis, and increased mitotic figures. Immunohistochemical staining exhibited positive staining for WT1, D2-40, and calretinin, supporting the mesothelial origin of the tumor. Notably, BerEP4 staining was negative, arguing against carcinoma. Immunostaining for keratin 5 was positive, supporting the mesothelial differentiation. The Ki67 proliferation index was high. The differential diagnosis included adenomatoid tumors, germ cell tumors, and pleomorphic sarcoma. We aim to discuss the clinical presentation, diagnostic approach, and therapeutic approaches of this rare entity.

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恶性睾丸旁间皮瘤:一名既往未接触过石棉的老年男性阴道鳞状上皮内的罕见病例。
阴道鳞状上皮恶性间皮瘤是一种极为罕见的侵袭性肿瘤,常发生在老年患者身上。由于阴道鳞状上皮恶性间皮瘤并不常见,且临床表现无特异性,因此诊断难度很大。组织病理学检查和免疫组化染色对于将这种肿瘤与其他睾丸旁肿块区分开来并确定诊断至关重要。早期发现和综合治疗计划对于改善这种罕见恶性肿瘤患者的预后和总体疗效至关重要。我们报告了一名78岁男性患者的阴道外膜恶性间皮瘤,该患者无石棉接触史,出现左侧睾丸旁巨大浸润性肿块。组织病理学检查显示,该瘤由上皮样细胞和纺锤形细胞组成,呈双相增殖,具有浸润特征、坏死灶和有丝分裂增快。免疫组化染色显示 WT1、D2-40 和 calretinin 染色阳性,支持肿瘤来源于间皮细胞。值得注意的是,BerEP4 染色呈阴性,这证明肿瘤不是癌。角蛋白 5 免疫染色呈阳性,支持间皮分化。Ki67 增殖指数很高。鉴别诊断包括腺瘤样肿瘤、生殖细胞肿瘤和多形性肉瘤。我们旨在讨论这一罕见病例的临床表现、诊断方法和治疗方法。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
198
审稿时长
1 months
期刊介绍: International Journal of Surgical Pathology (IJSP) is a peer-reviewed journal published eight times a year, which offers original research and observations covering all major organ systems, timely reviews of new techniques and procedures, discussions of controversies in surgical pathology, case reports, and images in pathology. This journal is a member of the Committee on Publication Ethics (COPE).
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