Perez Anthony, Arcilla Crisostomo, Fontanilla Maria Raisa Katrina, Berberabe Apolinario Ericson
University of the Philippines Manila College of Medicine, Department of Surgery, Philippines; Manila Doctors Hospital, Philippines.
University of the Philippines Manila College of Medicine, Department of Surgery, Philippines; Manila Doctors Hospital, Philippines.
Int J Surg Case Rep. 2021 Nov;88:106526. doi: 10.1016/j.ijscr.2021.106526. Epub 2021 Oct 18.
Solid Pseudopapillary Neoplasm (SPN) is a rare pancreatic neoplasm with low malignant potential and a relative indolent course. Complete resection of the SPN is curative for most cases and has a high survival rate. Recurrences, though rare, can still occur despite adequate resection. Pancreaticoduodenectomy is commonly performed to treat pancreatic head SPNs. In recent years, duodenum-preserving pancreatic head resection (DPPHR) has been reported as a less radical and acceptable alternative.
We are reporting a case of 26-year old female who presented with a 7 month history of epigastric pain and increasing abdominal girth. She was diagnosed by MRI to have a huge but resectable pancreatic head mass and subsequently underwent duodenum-preserving pancreatic head resection (DPPHR) with pancreaticojejunostomy. Histopathologic examination revealed a solid pseudopapillary tumor (SPN) with lymphovascular invasion and negative margins of resection. The patient underwent hepaticojejunostomy 5 months after resection for biliary stricture. Surveillance imaging revealed tumor recurrence warranting re-exploration for recurrence 3 years after the initial surgery. Intraoperative findings revealed the mass at the distal pancreatic remnant, requiring distal pancreatectomy and splenectomy.
Solid pseudopapillary neoplasms are rare pancreatic neoplasms. Surgical resection of SPNs affords long term cure with good 5-year survival rates for localized tumors Despite the low malignant potential of SPNs, relapse after resection can still occur.
Complete local resection of the tumor is the treatment of choice in SPNs. DPPHR should be considered as an alternative in young patients with a localized SPN in the pancreatic head.
实性假乳头状肿瘤(SPN)是一种罕见的胰腺肿瘤,恶性潜能低,病程相对惰性。大多数情况下,完整切除SPN可治愈,生存率高。复发虽罕见,但即使切除充分仍可能发生。胰十二指肠切除术常用于治疗胰头SPN。近年来,保留十二指肠的胰头切除术(DPPHR)已被报道为一种创伤较小且可接受的替代方法。
我们报告一例26岁女性患者,有7个月上腹部疼痛和腹围增大病史。磁共振成像(MRI)诊断为巨大但可切除的胰头肿块,随后接受了保留十二指肠的胰头切除术(DPPHR)并进行了胰空肠吻合术。组织病理学检查显示为实性假乳头状肿瘤(SPN),伴有脉管侵犯,切缘阴性。患者术后5个月因胆管狭窄接受了肝空肠吻合术。监测影像学显示肿瘤复发,在初次手术后3年需要再次手术探查复发情况。术中发现肿块位于胰腺远端残余部分,需要进行远端胰腺切除术和脾切除术。
实性假乳头状肿瘤是罕见的胰腺肿瘤。手术切除SPN可实现长期治愈,局部肿瘤的5年生存率良好。尽管SPN恶性潜能低,但切除后仍可能复发。
肿瘤的完整局部切除是SPN的首选治疗方法。对于胰头局限性SPN的年轻患者,应考虑DPPHR作为一种替代方法。