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Malignant mesothelioma of tunica vaginalis testis: Report of a very rare case with review of the literature

机译:阴道膜睾丸恶性间皮瘤:非常罕见的病例报道并文献复习

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Introduction: Mesothelioma of the tunica vaginalis testis is a extremely rare tumor and represents 0.3 to 0.5% of all malignant mesotheliomas. Exposure to asbestos often precedes illness. Because of its low incidence and nonspecific clinical presentation, it is mostly diagnosed accidentally during surgery for other reasons and the prognosis is usually poor. We present a case of a patient with a mesothelioma of tunica vaginalis testis, diagnosed secondarily during hydrocele surgery, with long-term survival after radical surgery. Materials and methods: a 40 years old patient was admitted to our department for routine surgery of a left hydrocele. During the operation a frozen section analysis was requested because of the unusual nodular thickening of the tunica vaginalis: the examination revealed a diffuse malignant mesothelioma with epithelioid structure and tubular-papillary proliferation. Therefore a left hemi-scrotectomy with left inguinal lymph node dissection was performed. Results: The definitive histology confirmed the previous report of diffuse malignant mesothelioma with angio-invasion but normal testicle findings and negative lymph nodes. No metastases were found on the CT-scan. For the first 2 years a CT was repeated every 4 months, for other 3 years every 6 months and then yearly. Six years after surgery the patient is classified as no evidence of disease. Conclusions: malignant mesothelioma of the tunica vaginalis testis is a rare entity, often initially thought to be a hydrocele or an epididymal cyst. An aggressive approach with hemiscrotectomy with or without inguinal and retroperitoneal lymphadenectomy can reduce the risk of recurrence.
机译:简介:阴道膜睾丸间皮瘤是一种极为罕见的肿瘤,占所有恶性间皮瘤的0.3%至0.5%。接触石棉通常先于疾病。由于它的低发病率和非特异性的临床表现,多数是由于其他原因在手术中被意外诊断的,并且预后通常很差。我们介绍了一例患有睾丸间皮瘤的患者,该患者在鞘膜积液手术中被第二次诊断,根治性手术后可长期生存。材料和方法:一名40岁的患者被收治到我科接受左鞘膜积液的常规手术。在手术中,由于阴道膜的异常结节增厚,要求进行冷冻切片分析:检查发现弥漫性恶性间皮瘤具有上皮样结构和肾小管-乳头状增生。因此,进行了左半结肠切除术和左腹股沟淋巴结清扫术。结果:明确的组织学证实了先前报道的弥漫性恶性间皮瘤伴血管浸润,但睾丸检查结果正常,淋巴结阴性。在CT扫描中未发现转移。在头2年中,每4个月重复一次CT,其他3年每6个月一次,然后每年一次。手术六年后,该患者被分类为无疾病迹象。结论:阴道膜睾丸恶性间皮瘤是一种罕见的实体,通常最初被认为是鞘膜积液或附睾囊肿。积极行半结肠切除术,伴或不伴腹股沟和腹膜后淋巴结清扫术可以降低复发风险。

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