Valabrega S, Barillari P, De Angelis R, Di Lorenzo N, Gozzo P, Ramacciato G, Indinnimeo M
Cattedra di I Clinica Chirurgica, Università La Sapienza, Roma.
Ital J Surg Sci. 1987;17(3):257-9.
A 20-year-old man with congenital choledochal dilatation associated with carcinoma was treated. At the age of 10 years he underwent a cholecystectomy and partial resection of the cyst. At admission the patient complained of hypochondriac and back pain combined with bilious vomiting. He underwent a palliative operation. A review of the literature is presented on treatment and prognosis of patients with carcinoma arising in choledochal congenital dilatation previously treated by surgery other than excision. It is emphasized that the cystic dilatation should be removed at the time of the first operation. Furthermore, in patients who underwent surgical treatment without excision of the choledochal dilatation, the dilated biliary tract should be removed even in absence of subjective symptoms.
一名患有先天性胆总管扩张症并伴有癌症的20岁男性接受了治疗。他在10岁时接受了胆囊切除术和囊肿部分切除术。入院时,患者主诉季肋部和背部疼痛,并伴有胆汁性呕吐。他接受了姑息性手术。本文对先前接受过非切除术的先天性胆总管扩张症患者发生癌症的治疗和预后进行了文献综述。强调应在首次手术时切除囊性扩张。此外,对于未切除胆总管扩张而接受手术治疗的患者,即使没有主观症状,也应切除扩张的胆道。