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胰腺神经鞘瘤:两例报告并文献复习

Pancreatic schwannoma: report of two cases and review of the literature.

作者信息

Feldman L, Philpotts L E, Reinhold C, Duguid W P, Rosenberg L

机构信息

Department of Surgery, McGill University, Montreal, Quebec, Canada.

出版信息

Pancreas. 1997 Jul;15(1):99-105.

PMID:9211499
Abstract

Solitary intrapancreatic schwannoma is a rare tumor. We present two patients with this tumor and review 13 previously reported cases from the English-language literature. While the final diagnosis was made based on pathological examination of the tumors, both computed tomography scan and magnetic resonance imaging helped establish the benign nature of the lesion, narrow the differential diagnosis, and define the anatomical locations of the small tumors. Both tumors were treated by enucleation from the surrounding pancreatic parenchyma, and both patients, after 2 years of follow-up, are alive and well. It is concluded that multimodality radiologic investigations are useful in the workup of unusual pancreatic masses. In addition, based on the known biologic behavior of schwannomas occurring elsewhere in the body, simple enucleation, rather than more radical resection, is likely to be adequate therapy for these tumors.

摘要

孤立性胰腺内神经鞘瘤是一种罕见的肿瘤。我们报告了两名患有这种肿瘤的患者,并回顾了英文文献中先前报道的13例病例。虽然最终诊断是基于肿瘤的病理检查,但计算机断层扫描和磁共振成像都有助于确定病变的良性性质、缩小鉴别诊断范围并明确小肿瘤的解剖位置。两个肿瘤均通过从周围胰腺实质中摘除进行治疗,两名患者在随访2年后均存活且状况良好。结论是多模态放射学检查在不寻常胰腺肿块的检查中很有用。此外,基于身体其他部位发生的神经鞘瘤已知的生物学行为,单纯摘除而非更激进的切除可能是这些肿瘤的充分治疗方法。

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