高春涛, 赵天锁, 郝继辉. 50 例胰腺实性假乳头状瘤的临床诊治分析[J]. 中国肿瘤临床, 2017, 44(4): 173-176. DOI: 10.3969/j.issn.1000-8179.2017.04.387
引用本文: 高春涛, 赵天锁, 郝继辉. 50 例胰腺实性假乳头状瘤的临床诊治分析[J]. 中国肿瘤临床, 2017, 44(4): 173-176. DOI: 10.3969/j.issn.1000-8179.2017.04.387
GAO Chuntao, ZHAO Tiansuo, HAO Jihui. 50 cases of clinical diagnosis and treatment of solid-pseudopapillary tumor of pancreas[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(4): 173-176. DOI: 10.3969/j.issn.1000-8179.2017.04.387
Citation: GAO Chuntao, ZHAO Tiansuo, HAO Jihui. 50 cases of clinical diagnosis and treatment of solid-pseudopapillary tumor of pancreas[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(4): 173-176. DOI: 10.3969/j.issn.1000-8179.2017.04.387

50 例胰腺实性假乳头状瘤的临床诊治分析

50 cases of clinical diagnosis and treatment of solid-pseudopapillary tumor of pancreas

  • 摘要:
      目的  探讨胰腺实性假乳头状瘤的临床特点、影像学表现、病理特征、治疗方法与预后情况,为进一步提高其诊疗水平提供依据。
      方法  收集2011年1月至2016年10月天津医科大学肿瘤医院收治的50例胰腺实性假乳头状瘤患者的临床资料,回顾性分析其临床特征及诊治情况并行随访,对患者的病例资料、病理特征、诊疗方法和预后等进行总结。
      结果  50例患者年龄11~58岁,平均年龄(33±12)岁;临床表现多为查体发现腹部占位就诊。肿瘤多位于胰头部和体尾部。患者均行手术切除治疗,多为胰十二指肠切除术或脾胰体尾切除术。术后组织病理学检查已明确诊断为胰腺实性假乳头状瘤。住院时间为(13.90±5.16)d。对50例患者均进行随访,随访时间为3~70个月,49例患者未见复发或转移,所有患者均存活至今。
      结论  胰腺实性假乳头状瘤是一种较为罕见的低恶性胰腺肿瘤,多见于青年女性,其临床表现和实验室检查等无明显特异性,肿瘤标志物多阴性。切除肿瘤后能获得良好的预后。

     

    Abstract:
      Objective   This study explored the clinical characteristics, imaging features, biological characteristics, treatment, and prognosis of solid-pseudopapillary tumor of the pancreas (SPT).
      Methods   We collected clinical data of 50 cases of SPT in Tianjin Medical University Cancer Istitute and Hospital from January 2011 to October 2016. We then retrospectively reviewed and analyzed clinical and pathological features of these patients. We conducted follow-up consultations and summarized data on patient characteristics, pathological features, diagnosis, treatment, and prognosis.
      Results   Among 50 SPT patients, mean age was 33.0±12.00 years, and maleto- female ratio was 1:5.25. Clinical presentation was mostly an abdominal placeholder diagnosed by physical examination, and tumor was usually located in the head or body and tail of the pancreas. All patients received surgery; procedures included pancreaticoduodenectomy, and distal pancreatectomy plus spleen resection. SPT was clearly diagnosed with postoperative histopathological examination. Hospital stay lasted for 13.9±5.16 days. All 50 cases were followed up, with consultation period lasting for 3-70 months. No recurrence or metastasis appeared in 49 cases, and perioperative death was not noted in our patients.
      Conclusion   SPT is a rare, potential low-grade malignant tumor, which mostly affects young females. There is no obvious specificity in the clinical manifestation and laboratory examination. Tumor marker levels are almost within normal range. Surgery for SPT provides good prognosis and long survival duration.

     

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