Takeyoshi I, Suda Y, Sekine T, Uchida K, Hirata T, Saifuku K, Nakagawa T, Tanino M
Dept. of Abdominal Surgery, Saitama Cancer Center Hospital.
Gan No Rinsho. 1990 Jan;36(1):91-6.
Reported is a rare superficial papillary adenocarcinoma arising from a congenital cyst, along with a survey of pertinent cases in the world literature. A 43-year-old male with a huge hepatic cyst was admitted to hospital for further examination. Since the cystic drainage done for alcoholic fixation was seromucinous initially but later contaminated by bile, an operation was initiated for dome resection and the closure of the biliary communication. At the time of the deroofing, however, small granulomas were found. And those were confirmed as being malignant by frozen section. Thus, an extended right lobectomy was performed for therapy. From its history and nature, this was considered to be a cancer arising in a congenital hepatic cyst.
报告了一例罕见的起源于先天性囊肿的浅表乳头状腺癌,并对世界文献中的相关病例进行了综述。一名患有巨大肝囊肿的43岁男性因进一步检查入院。由于用于酒精固定的囊肿引流最初为浆液性,但后来被胆汁污染,因此开始进行囊肿顶部切除和胆道交通闭合手术。然而,在去顶时发现了小肉芽肿。经冰冻切片证实为恶性。因此,进行了扩大右叶切除术进行治疗。从其病史和性质来看,这被认为是一种起源于先天性肝囊肿的癌症。