Morris Mw, Anderson Cd, Drake Lc, Redfield Sm, Subramony C, Vanderlan Wb
University of Mississippi School of Medicine, Jackson, USA.
J Surg Case Rep. 2012 Sep 1;2012(9):15. doi: 10.1093/jscr/2012.9.15.
Biliary cystadenoma (BCA) is a rare cystic tumor which originates from intrahepatic or extrahepatic biliary ducts. Intrahepatic BCAs are more common, demonstrate a female predominance, and generally asymptomatic. Radiographic evaluation assists in the preoperative differentiation of these tumors from other cystic liver masses while resection remains the only means for definitive diagnosis. We report a case of massive mucinous intrahepatic BCA initially diagnosed as a nonresectable malignancy presenting in a female patient with progressively increasing abdominal pain and girth. Enucleation of the mass with non-anatomic resection was employed for surgical management of this intrahepatic BCA.
胆管囊腺瘤(BCA)是一种罕见的囊性肿瘤,起源于肝内或肝外胆管。肝内BCA更为常见,女性居多,通常无症状。影像学评估有助于术前将这些肿瘤与其他肝囊肿性肿块相鉴别,而切除仍是明确诊断的唯一方法。我们报告一例巨大黏液性肝内BCA病例,最初被诊断为不可切除的恶性肿瘤,该患者为女性,出现进行性加重的腹痛和腹围增大。采用肿物剜除术及非解剖性切除对该肝内BCA进行手术治疗。