AbuDalu M, Munz Y, Ohana G
Department of General Surgery, Barzilai Medical Center, Ashkelon, Israel.
Front Surg. 2023 May 24;10:1171234. doi: 10.3389/fsurg.2023.1171234. eCollection 2023.
An intraductal papillary mucinous neoplasm (IPMN) is a potentially malignant cystic tumor that is characterized by an excessive papillary proliferation of mucin-producing epithelial cells. The IPMN usually exhibits different degrees of dysplasia and is accompanied by cystic dilation of the main pancreatic duct (MPD) or side branch. We report a case of an IPMN that has penetrated the stomach and has differentiated into an adenocarcinoma.
A 69-year-old female, suffering from chronic pancreatitis of unknown etiology, visited our outpatient clinic with complaints of sudden weight loss, diarrhea, and abdominal pain. She underwent several examinations to evaluate the reasons for her sudden onset of symptoms. A gastroscopy showed an ulcerated lesion covered with mucus. CT and magnetic resonance cholangiopancreatography images revealed that the MPD was dilated to 1.3 cm with a fistula formation between the MPD and the stomach. After a multidisciplinary discussion of this case, a total pancreatectomy was proposed. An total pancreatectomy with gastric wedge resection including the fistula together with splenectomy was carried out. A Roux-en-Y choledochojejunostomy and gastrojejunostomy were performed. Histology results revealed the association of IPMN with invasive carcinoma.
Many reports on IPMN of the pancreas have been published recently. Fistula formation between IPMN and adjacent organs is possible. Given the CT and endoscopic ultrasonography findings, it shows that in our case a main duct IPMN (MD-IPMN) formed a pancreatico-gastric fistula. We point out that the adherence of invasive cancer cells contributed to the fistula formation between the pancreas and the stomach.
This case report provides evidence for the possibility of IPMN becoming complicated with pancreatico-gastric fistula. Thus, we suggest that surgical resection should be considered in the case of MD-IPMN because of its high propensity for malignant transformation.
导管内乳头状黏液性肿瘤(IPMN)是一种潜在的恶性囊性肿瘤,其特征是产生黏液的上皮细胞过度乳头状增生。IPMN通常表现出不同程度的发育异常,并伴有主胰管(MPD)或分支的囊性扩张。我们报告一例IPMN穿透胃并分化为腺癌的病例。
一名69岁女性,患有病因不明的慢性胰腺炎,因突然体重减轻、腹泻和腹痛前来我院门诊就诊。她接受了多项检查以评估症状突然发作的原因。胃镜检查显示有一个覆盖着黏液的溃疡病变。CT和磁共振胰胆管造影图像显示,MPD扩张至1.3 cm,MPD与胃之间形成瘘管。经过对该病例的多学科讨论,建议进行全胰切除术。实施了包括瘘管在内的全胰切除术加胃楔形切除术以及脾切除术。进行了Roux-en-Y胆总管空肠吻合术和胃空肠吻合术。组织学结果显示IPMN与浸润性癌有关。
最近发表了许多关于胰腺IPMN的报告。IPMN与相邻器官之间可能形成瘘管。根据CT和内镜超声检查结果,在我们的病例中显示一个主胰管IPMN(MD-IPMN)形成了胰胃瘘。我们指出,浸润性癌细胞的黏附促成了胰腺与胃之间的瘘管形成。
本病例报告为IPMN并发胰胃瘘的可能性提供了证据。因此,我们建议对于MD-IPMN病例应考虑手术切除,因为其恶性转化的倾向较高。