Liu Hang, Xu Zhiquan, Wang Yaxu, Gu Haitao, Tang Yunhao, Wu Dabin, Wang Jijian, Zhang Jianbo
Department of Gastrointestinal Surgery, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Front Surg. 2022 Nov 4;9:1020044. doi: 10.3389/fsurg.2022.1020044. eCollection 2022.
Solid pseudopapillary neoplasm (SPN) is a rare tumor with low malignant potential, which typically occurs in the pancreas. Extrapancreatic SPN is also extremely rare worldwide.
We report a case of a 70-year-old woman hospitalized with abdominal pain and bloating. The patient did not have any underlying diseases, such as diabetes, coronary heart disease, or hypertension. More than 30 years ago, the patient underwent surgery for "ectopic pregnancy". The patient had no family history of hereditary disease, nor did any immediate family members have a history of cancer. Laboratory tests showed that her hemoglobin and albumin levels were low and she had a high level of cancer antigen 125 (CA125). Enhanced computed tomography (CT) showed a large tumor in the abdomen and pelvis. The patient subsequently underwent surgery, and it was found that the tumor was attached to the terminal ileum. Pathological findings suggested that the tumor was an extrapancreatic SPN, with an ectopic pancreas found in the tumor tissue. The patient did not receive chemotherapy or radiotherapy after surgery. After 13 months of follow-up, the patient was admitted again with abdominal pain. CT showed tumor recurrence with extensive systemic metastases. The patient and her family refused reoperation and biopsy, and the patient was discharged after the abdominal pain and anemia resolved.
We report a rare case of extrapancreatic SPN of ileal origin, which could be the first report worldwide. It had aggressive biological features, with recurrence and metastasis 13 months after surgery. For extrapancreatic SPN, the risk of recurrence should be assessed, and for tumors suspected of malignant behavior, a longer follow-up after discharge may be needed. Although SPN generally has a good prognosis after surgery, there is no consensus on whether postoperative chemotherapy and other treatments are needed for patients with high recurrence risk.
实性假乳头状瘤(SPN)是一种恶性潜能较低的罕见肿瘤,通常发生于胰腺。胰腺外SPN在全球范围内也极为罕见。
我们报告一例70岁因腹痛和腹胀住院的女性病例。该患者无任何基础疾病,如糖尿病、冠心病或高血压。30多年前,该患者因“异位妊娠”接受过手术。患者无遗传性疾病家族史,直系亲属也无癌症病史。实验室检查显示其血红蛋白和白蛋白水平较低,癌抗原125(CA125)水平较高。增强计算机断层扫描(CT)显示腹部和盆腔有一个大肿瘤。患者随后接受手术,发现肿瘤附着于回肠末端。病理结果提示该肿瘤为胰腺外SPN,肿瘤组织中发现异位胰腺。患者术后未接受化疗或放疗。随访13个月后,患者因腹痛再次入院。CT显示肿瘤复发并伴有广泛的全身转移。患者及其家属拒绝再次手术和活检,腹痛和贫血缓解后出院。
我们报告一例罕见的回肠起源的胰腺外SPN病例,可能是全球首例报告。它具有侵袭性生物学特征,术后13个月复发并转移。对于胰腺外SPN,应评估复发风险,对于怀疑有恶性行为的肿瘤,出院后可能需要更长时间的随访。虽然SPN术后一般预后良好,但对于复发风险高的患者术后是否需要化疗及其他治疗尚无共识。