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巨大盆腔神经鞘瘤:病例报告及文献复习。

Giant Pelvic Schwannoma: Case Report and Review of the Literature.

机构信息

Emergency Surgery Department, St. Orsola University Hospital, Bologna, Italy.

Pathological Anatomy Department, St. Orsola University Hospital, Bologna, Italy.

出版信息

Dig Dis Sci. 2020 May;65(5):1315-1320. doi: 10.1007/s10620-020-06128-2.

Abstract

INTRODUCTION

Pelvic schwannomas are rare, mostly benign tumors. They are usually asymptomatic until their massive growth compresses adjacent organs. We describe the case of a 53-year-old man with a pelvic schwannoma who initially complained of constipation and urinary retention.

AREAS COVERED

We analyzed the clinical presentation, histopathology, diagnostic imaging tools, and the treatment options for pelvic schwannomas, compared with the few other cases reported in the literature.

EXPERT COMMENTARY

Pelvic schwannomas are masses that can grow to considerable size, producing symptoms over time. Due to their size and localization, surgery, although difficult, is the only available treatment.

摘要

简介

盆腔神经鞘瘤罕见,多为良性肿瘤。在巨大生长压迫临近器官前,通常无症状。我们描述了一位 53 岁男性盆腔神经鞘瘤患者的病例,其最初主诉为便秘和尿潴留。

涵盖范围

我们分析了该病例的临床表现、组织病理学、诊断影像学手段,以及与文献中少数其他病例相比的治疗选择。

专家评论

盆腔神经鞘瘤是可以生长到相当大体积的肿块,随着时间的推移会产生症状。由于其大小和位置,手术虽然困难,但却是唯一可行的治疗方法。

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