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Malignant Mesothelioma of Tunica Vaginalis Testis: Macroscopic and Microscopic Features of a Very Rare Malignancy

机译:阴道睾丸恶性间皮瘤:非常罕见恶性肿瘤的宏观和微观特征

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Malignant mesothelioma of the tunica vaginalis testis (MMTVT) is an extremely rare tumour, usually mimicking benign pathologies of the scrotum. Our case is an 84-year-old male patient who appealed with a painless, left-sided scrotal swelling longer than 2 months. Although the level of tumour markers was?normal, ultrasonographic examination results forced us to perform an inguinal scrotal exploration. Multiple small papillary tumours, both on tunica vaginalis and tunica albuginea, were?detected intraoperatively. Due to these findings, radical orchiectomy was performed. A?pathological evaluation showed malignant mesothelioma (MM) of the tunica vaginalis testis. Exposure to asbestos?is a well-known risk factor. Furthermore, a history of trauma, herniorrhaphy and chronic hydroceles is blamed as a possible risk factor. Scrotal ultrasonography is the mainstay of primary diagnosis and, therefore, it should not be overlooked when dealing with benign scrotal cysts or hydroceles, which are very common pathologies at these decades, too. Radical inguinal orchiectomy is the primary treatment choice for localised MMTVT disease,?whereas in signs of lymph node metastasis, inguinal lymph node dissection is required. Radical resection should be completed with?chemotherapy and/or radiotherapy for an?advanced or recurrent disease. This case, which is?very rarely reported in the literature and detected during inguinal exploration, along with the pathological works that supported the diagnosis, was presented with this report.
机译:阴道膜睾丸的恶性间皮瘤(MMTVT)是一种极为罕见的肿瘤,通常模仿阴囊的良性病变。我们的病例是一位84岁的男性患者,他的病痛无痛,左侧阴囊肿胀超过2个月。尽管肿瘤标志物水平正常,但超声检查结果迫使我们进行了腹股沟阴囊探查。术中在阴道膜和白膜上发现多个乳头状小瘤。由于这些发现,进行了根治性睾丸切除术。病理评估显示阴道膜睾丸有恶性间皮瘤(MM)。接触石棉是一个众所周知的危险因素。此外,将外伤,疝气和慢性鞘膜积液的病史归咎为可能的危险因素。阴囊超声检查是初步诊断的主要手段,因此,在治疗良性阴囊囊肿或鞘膜积液时,也不应忽视它,这也是近几十年来非常常见的病理。根治性腹股沟睾丸切除术是局部MMTVT疾病的主要治疗选择,而在淋巴结转移的迹象中,需要进行腹股沟淋巴结清扫术。对于晚期或复发性疾病,应通过化学疗法和/或放射疗法完成根治性切除。该病例在文献中很少报道,在腹股沟探查中发现,并伴有支持该诊断的病理学表现。

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