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1例冯雷克林霍增氏病患者的神经纤维瘤表现为恶性神经鞘瘤。病例报告。

Neurofibroma in a patient with von Recklinghausen's disease seen as a malignant schwannoma. A case report.

作者信息

Menendez L R, DiCesare P E, Soto C

机构信息

Department of Orthopaedics, University of Southern California School of Medicine, Los Angeles.

出版信息

Clin Orthop Relat Res. 1990 May(254):298-302.

PMID:2108836
Abstract

A rapidly growing, malignant schwannoma occurred in a 46-year-old woman with neurofibromatosis. Computed tomography, isotope bone scan, chest roentgenogram, and angiogram are helpful in determining the local extent and distant spread of such musculoskeletal tumors and are useful in planning appropriate surgical management. A well-planned biopsy, however, is essential to accurately determine the histologic diagnosis of the tumor. Clinical and roentgenographic presentation of some benign lesions may mimic malignant tumors. To confirm the diagnosis of a malignant or benign tumor, it is advisable to examine the musculoskeletal tumor histologically before proceeding with the definitive treatment, even if the clinical presentation strongly suggests malignancy.

摘要

一名患有神经纤维瘤病的46岁女性发生了快速生长的恶性神经鞘瘤。计算机断层扫描、同位素骨扫描、胸部X线片和血管造影有助于确定此类肌肉骨骼肿瘤的局部范围和远处转移,对规划适当的手术治疗很有用。然而,精心规划的活检对于准确确定肿瘤的组织学诊断至关重要。一些良性病变的临床和X线表现可能类似于恶性肿瘤。为了确诊恶性或良性肿瘤,即使临床表现强烈提示为恶性,在进行确定性治疗之前,对肌肉骨骼肿瘤进行组织学检查是明智的。

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