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血管活性肠肽分泌肿瘤:综述。

Vasoactive Intestinal Peptide-Secreting Tumors: A Review.

机构信息

From the Department of Internal Medicine, UCONN Health, Farmington, CT.

Gastroenterology Division, Mayo Clinic, Rochester, MN.

出版信息

Pancreas. 2019 Oct;48(9):1119-1125. doi: 10.1097/MPA.0000000000001402.

Abstract

Vasoactive intestinal peptide-secreting tumors (VIPomas) are a group of rare neuroendocrine tumors, which cause a typical syndrome of watery diarrhea. Most of these tumors are found in the pancreas and are usually detected at a later stage. Although curative resection is not possible in most of these tumors, both symptom and tumor control can be achieved by a multidimensional approach, to enable a long survival of most patients. There are no clear-cut guidelines for the management of VIPomas because of the rarity of this neoplasm and lack of prospective data. In this review, we discuss the available evidence on the clinical features and management of these rare tumors.

摘要

血管活性肠肽瘤(VIPomas)是一组罕见的神经内分泌肿瘤,可引起典型的水样腹泻综合征。这些肿瘤大多数发生在胰腺,通常在晚期才被发现。尽管大多数肿瘤无法进行根治性切除,但通过多维度的方法可以控制症状和肿瘤,使大多数患者获得长期生存。由于这种肿瘤罕见且缺乏前瞻性数据,因此对于 VIPomas 的治疗尚无明确的指南。在这篇综述中,我们讨论了关于这些罕见肿瘤的临床特征和治疗的现有证据。

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