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The first case of benign multicystic mesothelioma presenting as a splenic mass

机译:首例良性多囊性间皮瘤表现为脾肿块

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摘要

Multicystic mesothelioma (MM) is a relatively rare tumour arising in the pelvic peritoneum of the tuboovarian region of young woman. Exceptionally, MM occurs on the serosal surfaces of various organs including kidney, bladder, lymph nodes, and liver. We report here the first case of MM wherein a 58-year-old woman with a previous history of endometriosis of the right ovary presented with a large multicystic mass of the spleen. The diagnosis of MM was made on a surgical specimen after splenectomy. A histopathologic examination is always necessary for the diagnosis of MM which should be differentiated from other lesions particularly from cystic lymphangioma. At one year follow-up, the patient had no evidence of recurrence. Despite the high frequency of local recurrences, MM is a benign lesion and ‘en bloc’ surgical excision with prolonged follow-ups is the treatment of choice.
机译:多囊性间皮瘤(MM)是一种相对罕见的肿瘤,发生在年轻女性的微管卵巢区域的盆腔腹膜中。 MM异常发生在包括肾脏,膀胱,淋巴结和肝脏在内的各种器官的浆膜表面。我们在这里报告的第一例MM,其中一名58岁的女性先前有右卵巢子宫内膜异位病史,表现为脾脏多囊性肿块。 MM的诊断是在脾切除术后的手术标本上进行的。 MM的诊断始终需要组织病理学检查,应与其他病变(尤其是囊性淋巴管瘤)区分开来。在一年的随访中,患者没有复发的迹象。尽管局部复发的频率很高,但是MM是一种良性病变,需要长期随访的“整块”手术切除是治疗的选择。

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