Zhang Yu, Cheng Heng-Hui, Fan Wen-Juan
Department of Gastroenterology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, China.
Institution of Pathology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, China.
World J Gastrointest Surg. 2023 Dec 27;15(12):2945-2953. doi: 10.4240/wjgs.v15.i12.2945.
Groove pancreatitis (GP) is a rare condition affecting the pancreatic groove region within the dorsal-cranial part of the pancreatic head, duodenum, and common bile duct. As a rare form of chronic pancreatitis, GP poses a diagnostic and therapeutic challenge for clinicians. GP is frequently misdiagnosed or not considered; thus, the diagnosis is often delayed by weeks or months. The treatment of GP is complicated and often requires surgical intervention, especially pancreatoduodenectomy.
A 66-year-old man with a history of long-term drinking was admitted to the gastroenterology department of our hospital, complaining of vomiting and acid reflux. Upper gastrointestinal endoscopy showed luminal stenosis in the descending part of the duodenum. Abdominal computed tomography showed slight exudation in the descending and horizontal parts of the duodenum with broadening of the groove region, indicating local pancreatitis. The symptoms of intestinal obstruction were not relieved with conservative therapy, and insertion of an enteral feeding tube was not successful. Exploratory laparoscopy was performed and revealed a hard mass with scarring in the horizontal part of the duodenum and stenosis. Intraoperative frozen section analysis showed no evidence of malignancy, and side-to-side duodenojejunostomy was performed. Routine pathologic examination showed massive proliferation of fibrous tissue, hyaline change, and the proliferation of spindle cells. Based on the radiologic and pathologic characteristics, a diagnosis of GP was made. The patient presented with anastomotic obstruction postoperatively and took a long time to recover, requiring supportive therapy.
GP often involves the descending and horizontal parts of the duodenum and causes duodenal stenosis, impaired duodenal motility, and gastric emptying due to fibrosis.
沟部胰腺炎(GP)是一种罕见疾病,累及胰头背侧上部、十二指肠和胆总管内的胰腺沟区域。作为一种罕见的慢性胰腺炎形式,GP给临床医生带来了诊断和治疗挑战。GP常被误诊或未被考虑到;因此,诊断往往延迟数周或数月。GP的治疗复杂,通常需要手术干预,尤其是胰十二指肠切除术。
一名有长期饮酒史的66岁男性因呕吐和反酸入住我院消化内科。上消化道内镜检查显示十二指肠降部管腔狭窄。腹部计算机断层扫描显示十二指肠降部和水平部有轻微渗出,沟区域增宽,提示局部胰腺炎。保守治疗后肠梗阻症状未缓解,肠内营养管置入未成功。进行了腹腔镜探查,发现十二指肠水平部有一个伴有瘢痕形成的硬块及狭窄。术中冰冻切片分析未发现恶性证据,遂行十二指肠空肠侧侧吻合术。常规病理检查显示纤维组织大量增生、玻璃样变及梭形细胞增生。根据影像学和病理特征,诊断为GP。患者术后出现吻合口梗阻,恢复时间长,需要支持治疗。
GP常累及十二指肠降部和水平部,因纤维化导致十二指肠狭窄、十二指肠动力受损及胃排空障碍。