線毛性前腸性肝嚢胞(ciliated hepatic foregut cyst)の1例-本邦報告例24例の検討-

智彦 万波, 嘉洋 大藤, 恵子 藤原, 勝弘 江野村, 徹哉 太田, 浩範 國末, 修一 野村, 香織 江口, 小田 和歌子, 一郎 山鳥, 晴弘 山下
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Abstract

We report a 52-year-old patient with a small hepatic mass which was ultrasonographically anechoic with scattered high echoic spots, and appearing slightly hyperattenuating relative to the surrounding parenchyma on unenhanced CT scans. Laparotomy revealed that the lesion was a unilocular cyst containing a mucinous fluid. The histologic diagnosis was ciliated hepatic foregut cyst (CHFC). The CHFC is a rare congenital cystic tumor which derives from the embryologic foregut. Up to 2006, only 24 cases, including our case, had been reported in Japan. The patients were 13 men and 11 women, aged between 41 years and 79 years. All of the lesions were solitary and unilocular. In 22 cases, the CHFC was located in the medial segment of the left lobe, mostly just beneath the hepatic surface. In all 24 Japanese cases, the cystic wall was benign histologically. However, reports of 3 malignant cases overseas indicates we should treat this disease cautiously.
线毛性肠前性囊肿(ciliated hepatic foregut, cyst) 1例-本邦报告24例的讨论-
我们报告一个52岁的病人,他有一个小的肝脏肿块,超声表现为无回声,有分散的高回声点,在CT非增强扫描上相对于周围的实质表现为轻微的高衰减。剖腹探查发现病变为含黏液的单眼囊肿。组织学诊断为纤毛肝前肠囊肿(CHFC)。CHFC是一种罕见的先天性囊性肿瘤,起源于胚胎前肠。截至2006年,日本仅报告了24例,包括我们的病例。患者男13例,女11例,年龄41 ~ 79岁。所有的病变都是孤立的、单眼的。22例CHFC位于左叶内侧段,多数位于肝表面下方。在所有24例日本病例中,囊壁在组织学上均为良性。然而,国外3例恶性病例的报道提示我们应谨慎对待此病。
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