Butterly L F, Schapiro R H, LaMuraglia G M, Warshaw A L
Department of Medicine, Harvard Medical School, Boston, Mass.
Surgery. 1988 Mar;103(3):328-34.
Two granular cell tumors of the biliary tree are described, one in a 37-year-old black woman with obstructive jaundice and the other in a 26-year-old white woman with abdominal pain. These are rare soft tissue tumors that have an excellent prognosis when surgically excised. Almost all reported cases have been in young women, the majority of whom have been black. Because granular cell tumors of the biliary tract are uniformly resectable and curable, they should be considered and distinguished from cholangiocarcinoma or localized sclerosing cholangitis, particularly if the patient is young, female, and black.
本文描述了两例胆管颗粒细胞瘤,一例发生在一名37岁患有梗阻性黄疸的黑人女性身上,另一例发生在一名26岁患有腹痛的白人女性身上。这些是罕见的软组织肿瘤,手术切除后预后良好。几乎所有报道的病例都发生在年轻女性中,其中大多数是黑人。由于胆管颗粒细胞瘤均可切除且可治愈,因此应予以考虑,并与胆管癌或局限性硬化性胆管炎相鉴别,特别是当患者为年轻女性且为黑人时。