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胰腺实性假乳头状瘤:单中心经验及文献综述

Solid Pseudopapillary Tumor of the Pancreas: A Single-center Experience and Review of the Literature.

作者信息

Antoniou Efstathios A, Damaskos Christos, Garmpis Nikolaos, Salakos Christos, Margonis Giorgos-Antonios, Kontzoglou Konstantinos, Lahanis Stefanos, Spartalis Eleftherios, Patsouras Dimitrios, Kykalos Stylianos, Garmpi Anna, Andreatos Nikolaos, Pawlik Timothy M, Kouraklis Gregory

机构信息

Second Department of Propedeutic Surgery, "Laiko" General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Second Department of Propedeutic Surgery, "Laiko" General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece

出版信息

In Vivo. 2017 Jul-Aug;31(4):501-510. doi: 10.21873/invivo.11089.

Abstract

BACKGROUND

Solid pseudopapillary tumors (SPTs) of the pancreas are a rare occurrence, not exceeding 1-2% of all exocrine pancreatic tumors. SPT was first described in 1959 as "papillary tumor of the pancreas, benign or malignant" and affects mainly young women, in their second or third decade of age. These tumors are of low malignant potential, unclear pathogenesis, grow gradually and become considerably large before causing symptoms. A typical clinical presentation is often described by affected patients and, in some cases, an SPT is an incidental finding during the time the patient undergoes medical imaging studies for other health issues. SPT is frequently located at the head or tail of the pancreas. Metastases are rare but, when present, affect predominantly the liver.

PATIENTS AND METHODS

We report a series of five SPT cases in female patients 13-47 years old, presenting with almost identical symptoms of upper abdominal discomfort and non-tender palpable mass. Two out of five patients also reported vomiting, nausea and poor appetite as co-existing non-diagnostic symptoms. Only one patient presented without any symptoms. Tumor location and dimensions varied. One patient underwent a pancreatoduodenectomy (Whipple's procedure), while the remaining patients underwent distal pancreatectomy with concomitant splenectomy.

RESULTS

Perioperative morbidity and mortality was zero. All five patients are disease-free at a follow-up from 3 months to 13 years. Histopathology reports supported the diagnosis of SPT and no metastatic disease was present in any of the patients.

CONCLUSION

The overall prognosis of SPT of the pancreas is excellent due to its favorable biological features, even in the presence of distal metastasis. Although surgical resection is often curative, a close follow-up is advised in order to diagnose a possible local recurrence or distal metastasis and choose the proper therapeutic option for the patients.

摘要

背景

胰腺实性假乳头状瘤(SPT)较为罕见,占所有胰腺外分泌肿瘤的比例不超过1%-2%。SPT于1959年首次被描述为“胰腺乳头状肿瘤,良性或恶性”,主要影响20到30岁的年轻女性。这些肿瘤恶性潜能低,发病机制不明,生长缓慢,在引起症状之前会长得相当大。受影响的患者通常会有典型的临床表现,在某些情况下,SPT是患者因其他健康问题进行医学影像检查时的偶然发现。SPT常位于胰腺头部或尾部。转移很少见,但一旦发生,主要影响肝脏。

患者与方法

我们报告了一系列5例SPT病例,患者为13至47岁的女性,均表现出几乎相同的上腹部不适症状和可触及的无压痛肿块。5名患者中有2名还报告伴有呕吐、恶心和食欲不振等非特异性症状。只有1名患者没有任何症状。肿瘤位置和大小各不相同。1例患者接受了胰十二指肠切除术(惠普尔手术),其余患者接受了远端胰腺切除术并同时切除脾脏。

结果

围手术期发病率和死亡率为零。所有5例患者在3个月至13年的随访中均无疾病复发。组织病理学报告支持SPT的诊断,所有患者均未出现转移性疾病。

结论

胰腺SPT因其良好的生物学特性,总体预后良好,即使存在远处转移也是如此。虽然手术切除通常可治愈,但建议密切随访,以便诊断可能的局部复发或远处转移,并为患者选择合适的治疗方案。

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