Vrettos M E, Kostopoulou E, Papavasileiou C, Sikas N, Agelidou S
B Department of Surgery, Hippokrateion Hospital of Thessaloniki, Konstantinoupoleos 49, Thessaloniki 54642, Greece.
Surg Endosc. 2000 Jun;14(6):595. doi: 10.1007/s004640000126. Epub 2000 Apr 28.
Primary mucinous cystadenoma of the mesocolon is a rare tumor with an uncertain histogenesis. A 38-year-old woman was diagnosed with a 17-cm cystic lesion in the left abdomen, identified as a mucinous cystadenoma of the mesocolon. This type of tumor appears rarely in extraovarian sites. We believe that metaplasia, either celomic or mucinous, is the most likely pathogenic mechanism. On rare occasions, a borderline or invasive component may be present.
结肠系膜原发性黏液性囊腺瘤是一种组织发生尚不明确的罕见肿瘤。一名38岁女性被诊断出左腹部有一个17厘米的囊性病变，经鉴定为结肠系膜黏液性囊腺瘤。这种肿瘤很少出现在卵巢外部位。我们认为化生，无论是间皮化生还是黏液化生，是最可能的致病机制。极少数情况下，可能会出现交界性或浸润性成分。
