Byard R W, Thorner P S, Cutz E, Filler R M, Durie P
Department of Histopathology, Adelaide Children's Hospital, Australia.
Pathology. 1990 Oct;22(4):239-41. doi: 10.3109/00313029009086671.
A unique complication of florid xanthogranulomatous cholecystitis with cholecystoduodenal fistula formation is described in a 6 yr old male. The patient, who had a short gut syndrome, had been maintained on lifelong total parenteral nutrition (TPN) following extensive neonatal ischemic bowel necrosis secondary to gastroschisis. Endoscopic duodenal mucosal biopsy demonstrated a granulomatous inflammatory infiltrate surrounding bile casts suggesting the possibility of a fistula between the biliary tract and duodenum. Additional clinical and radiological evidence of a cholecystoduodenal fistula prompted surgical intervention. At laparotomy the gallbladder was firmly bound to the duodenum by dense fibrous adhesions. Histologic examination showed xanthogranulomatous inflammation in association with fragments of bile that were present both within the gallbladder wall and within a fistulous tract in the adjacent connective tissue.
一名6岁男性患者出现了一种罕见的并发症,即伴有胆囊十二指肠瘘形成的 florid 黄色肉芽肿性胆囊炎。该患者患有短肠综合征,在因腹裂继发广泛的新生儿缺血性肠坏死之后,一直依靠终身全胃肠外营养(TPN)维持生命。内镜下十二指肠黏膜活检显示,胆汁铸型周围有肉芽肿性炎性浸润,提示胆道与十二指肠之间可能存在瘘管。胆囊十二指肠瘘的其他临床和影像学证据促使进行手术干预。剖腹手术时发现,胆囊通过致密的纤维粘连与十二指肠紧密相连。组织学检查显示,胆囊壁内以及相邻结缔组织的瘘管内均有黄色肉芽肿性炎症,并伴有胆汁碎片。