Nonomura A, Mizukami Y, Matsubara F, Ueda H
Pathology Section, Kanazawa University Hospital, School of Medicine, Kanazawa University, Japan.
J Gastroenterol. 1994 Oct;29(5):669-75. doi: 10.1007/BF02365455.
One complication of choledochal cyst in adulthood is the development of secondary carcinoma, usually well-differentiated adenocarcinoma. We report a case of extrahepatic bile duct carcinoma associated with choledochal cyst and presenting predominantly sarcomatous features. The patient was a 52-year-old female who presented with abdominal fullness and pain. Ultrasound (US), computed tomography (CT), and cholangiography revealed a choledochal cyst with a tumor. The resected choledochal cyst was 10 x 7.5 cm and contained a protruding, ulcerated tumor, measuring about 4.0 x 2.5 cm. Histologically, the tumor was composed of spindle-shaped or fusiform cells with occasional pleomorphic or bizarre giant cells and abundant fibrous stroma, similar to malignant mesenchymal tumors. However, further histologic and immunohistochemical examination revealed that the tumor was adenocarcinoma with prominent sarcomatous features. To our knowledge, sarcomatous change in extrahepatic bile duct carcinoma associated with choledochal cyst has not been previously described.
胆总管囊肿在成年期的一个并发症是继发性癌的发生,通常为高分化腺癌。我们报告一例与胆总管囊肿相关的肝外胆管癌,其主要表现为肉瘤样特征。患者为一名52岁女性,表现为腹部胀满和疼痛。超声(US)、计算机断层扫描(CT)和胆管造影显示胆总管囊肿合并肿瘤。切除的胆总管囊肿大小为10×7.5 cm,内有一突出的溃疡性肿瘤,大小约为4.0×2.5 cm。组织学上,肿瘤由梭形或纺锤形细胞组成,偶尔可见多形性或奇异的巨细胞以及丰富的纤维性间质,类似于恶性间叶性肿瘤。然而,进一步的组织学和免疫组化检查显示该肿瘤为具有显著肉瘤样特征的腺癌。据我们所知,此前尚未描述过与胆总管囊肿相关的肝外胆管癌的肉瘤样改变。