Arora Aditi, Singh Pradyumn, Anand Nidhi, Husain Nuzhat
Department of Pathology, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India
Department of Pathology, Dr Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.
BMJ Case Rep. 2017 Apr 10;2017:bcr-2016-218329. doi: 10.1136/bcr-2016-218329.
Choledochal cyst is a rare congenital malformation, particularly when associated with stones in cyst (cystolithiasis), gallstones and heterotopic pancreatic tissue within the cyst wall. The current case represents a 5-year-old boy with abdominal pain, pale colored stools, and jaundice. Magnetic resonance cholangiopancreatography showed a cystic lesion, arising from common bile duct with cystolithiasis and cholelithiasis. He underwent excision of choledochal cyst and gallbladder with Roux-en-Y hepaticojejunostomy. Microscopic examination showed a cyst wall composed of fibrocollagenous tissue lined by cuboidal to low columnar epithelium. The subserosal layer of cyst wall showed presence of heterotopic exocrine pancreatic tissue comprising of pancreatic acinar cells and ducts. We report the first case of heterotopic pancreatic tissue associated with choledochal cyst and cystolithiasis and cholelithiasis occurring at the same time.
胆总管囊肿是一种罕见的先天性畸形,尤其是当囊肿内伴有结石(囊肿结石病)、胆结石以及囊肿壁内的异位胰腺组织时。本病例为一名5岁男孩,有腹痛、浅色粪便和黄疸症状。磁共振胰胆管造影显示一个囊性病变,起源于胆总管,伴有囊肿结石病和胆结石。他接受了胆总管囊肿及胆囊切除术,并进行了 Roux-en-Y 肝空肠吻合术。显微镜检查显示囊肿壁由纤维胶原组织构成,内衬立方上皮至低柱状上皮。囊肿壁的浆膜下层显示存在异位外分泌胰腺组织,由胰腺腺泡细胞和导管组成。我们报告了首例同时出现胆总管囊肿、囊肿结石病、胆结石且伴有异位胰腺组织的病例。