Jones M A, Young R H, Scully R E
Department of Pathology, Maine Medical Center, Portland 04102, USA.
Am J Surg Pathol. 1995 Jul;19(7):815-25. doi: 10.1097/00000478-199507000-00010.
Eleven malignant mesotheliomas of the testicular tunica vaginalis occurred in patients aged 12 to 76 (mean, 54.1) years. Hydrocele, with or without an associated mass, or appreciation of a paratesticular mass accounted for the clinical presentation. One patient had a history of asbestos exposure. Grossly, the tumors typically presented as multiple nodules studding a hydrocele sac, frequently associated with a mass infiltrating the spermatic cord or adjacent testis. Microscopically, five tumors were epithelial and six biphasic, with the typical architectural and cytologic features of mesothelioma. Mixtures of papillary, tubular, and solid patterns predominated in the epithelial areas; interlacing fascicles of spindle cells with scanty stroma characterized the sarcomatous components. All eight of the tumors that were stained for keratin (AE1/AE3) were positive, four of five for epithelial membrane antigen, and four of five for vimentin. Seven of seven tumors were carcinoembryonic antigen negative and five of five B72.3, Leu-M1, and Ber-Ep4 negative. Follow-up ranging from 1 to 15 (mean, 4.3) years was available for seven patients. Three died of disease after 4, 4, and 3 years, and three are alive with disease 2, 2, and 15 years after diagnosis. Two of the latter three patients had extensive local recurrences, one 15 years after the diagnosis of a well-differentiated papillary mesothelioma, the other 2 years following treatment with hydrocelectomy only. One patient who has been followed for only 1 year has no evidence of disease. This series emphasizes a number of important features of testicular mesothelioma; (a) a wide age range with occasional occurrence at a young age, (b) a wide morphologic spectrum with regard to degree of differentiation, and (c) an aggressive natural history with a potential for late recurrence or metastasis of even well-differentiated tumors, suggesting the need for initial aggressive surgical treatment.
11例睾丸鞘膜恶性间皮瘤发生于12至76岁(平均54.1岁)的患者。鞘膜积液伴或不伴有相关肿块,或发现睾丸旁肿块构成临床表现。1例患者有石棉接触史。大体上,肿瘤通常表现为多个结节散布于鞘膜积液囊内,常伴有浸润精索或邻近睾丸的肿块。显微镜下,5例为上皮型,6例为双相型,具有间皮瘤典型的结构和细胞学特征。上皮区域以乳头、管状和实性结构混合为主;梭形细胞交织束状且间质稀少是肉瘤成分的特征。8例进行角蛋白(AE1/AE3)染色的肿瘤均为阳性,5例中有4例上皮膜抗原阳性,5例中有4例波形蛋白阳性。7例肿瘤癌胚抗原阴性,5例B72.3、Leu-M1和Ber-Ep4均阴性。7例患者有1至15年(平均4.3年)的随访资料。3例分别在4年、4年和3年后死于疾病,3例在诊断后2年、2年和15年仍患有疾病存活。后3例患者中有2例有广泛的局部复发,1例在诊断高分化乳头状间皮瘤15年后复发,另1例仅在进行鞘膜积液切除术后2年复发。1例仅随访1年的患者无疾病证据。该系列病例强调了睾丸间皮瘤的一些重要特征:(a)年龄范围广,偶见年轻患者发病;(b)在分化程度方面形态学谱广;(c)自然病程侵袭性强,即使是高分化肿瘤也有晚期复发或转移的可能,提示需要初始进行积极的手术治疗。