Meng Xianmin, Guzzo Thomas J, Bing Zhanyong
Department of Pathology and Laboratory Medicine;
Rare Tumors. 2013 Mar 26;5(1):e4. doi: 10.4081/rt.2013.e4. Print 2013 Feb 11.
Primary malignant mesothelioma (MM) of spermatic cord is extremely rare. We presented two malignant mesotheliomas involving the spermatic cords; one was primary, one secondary. The secondary one represented the direct involvement by a peritoneal MM. No occupational exposure to asbestos was identified in either patient. Both of them presented with a painless inguinal mass. Microscopically the primary MM was epithelioid type with tumor nests infiltrating adjacent adipose tissue, while the secondary MM grew in mixed type. No tumor necrosis was seen in the primary MM, while extensive necrosis was seen in the secondary one. Rare mitotic figure was seen in the primary MM while the mitosis in the secondary tumor was brisk, and with atypical mitosis. Immunohistochemically the tumor cells were positive for calretinin and CK5/6 and negative for BER-EP4 and BRST3 in both cases. The reported cases of primary MM from spermatic cord in English literature were briefly reviewed.
原发性精索恶性间皮瘤(MM)极为罕见。我们报告了两例累及精索的恶性间皮瘤;一例为原发性,一例为继发性。继发性病例表现为腹膜MM的直接累及。两名患者均未发现职业性石棉接触史。他们均表现为无痛性腹股沟肿块。显微镜下,原发性MM为上皮样型,肿瘤巢浸润相邻脂肪组织,而继发性MM为混合型生长。原发性MM未见肿瘤坏死,而继发性MM可见广泛坏死。原发性MM可见罕见的有丝分裂象,而继发性肿瘤有丝分裂活跃,且有非典型有丝分裂。免疫组化显示,两例肿瘤细胞钙结合蛋白和CK5/6均为阳性,BER-EP4和BRST3均为阴性。本文简要回顾了英文文献中报道的原发性精索MM病例。