Department of Pathology, The Ohio State University Wexner Medical Center, Columbus, USA.
Department of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Int J Surg Pathol. 2024 Sep;32(6):1117-1122. doi: 10.1177/10668969231215426. Epub 2024 Jan 2.
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.
睾丸鞘膜恶性间皮瘤是一种极其罕见且侵袭性强的肿瘤,常见于老年患者。由于其罕见性和非特异性临床表现,睾丸鞘膜恶性间皮瘤的诊断具有一定挑战性。组织病理学检查和免疫组织化学染色对于将该肿瘤与其他睾丸旁肿块区分开来并确立明确诊断至关重要。早期发现和全面的治疗计划对于改善这种罕见恶性肿瘤患者的预后和总体结局至关重要。我们报告了一例 78 岁男性患者的睾丸鞘膜恶性间皮瘤病例,该患者无石棉暴露史,表现为左侧巨大浸润性睾丸旁肿块。组织病理学检查显示为上皮样和梭形细胞的双相增生,具有浸润性特征、坏死灶和增加的有丝分裂象。免疫组织化学染色显示 WT1、D2-40 和钙视网膜蛋白阳性染色,支持肿瘤的间皮起源。值得注意的是,BerEP4 染色阴性,排除了癌。角蛋白 5 的免疫染色阳性,支持间皮分化。Ki67 增殖指数较高。鉴别诊断包括腺肌瘤、生殖细胞肿瘤和多形性肉瘤。我们旨在讨论这种罕见实体的临床表现、诊断方法和治疗方法。