Literature DB >> 24731456

[The value of soft tissue neurogenic tumors in the extremities with 3.0 T magnetic resonance imaging].

Xiaojuan Guo1, Huibo Zhang2, Min Liu1, Li Wang1, Tao Jiang1, Renyou Zhai1.   

Abstract

OBJECTIVE: To explore the diagnostic value of 3.0T MRI in neurogenic tumor of soft tissue in the extremities.
METHODS: The MRI appearance of 17 neurogenic tumors with pathological confirmation was retrospectively analyzed. Various imaging characteristics of tumors were evaluated and different imaging findings were compared. The diagnosis value of each MRI features was evaluated with receiver-operating-characteristics (ROC) analysis.
RESULTS: In the benign tumors significant differences between neurilemmoma and neurofibromas were noted for the position (P = 0.044). Heterogenicity on T(2)-weighted fat suppression images was also significant in differentiating between neurilemmoma and neurofibromas ( P = 0.020) . The shape of tumors, maximum length of tumor short diameter, edem around masses, relationship with adjoining fascia had the best discriminatory ability. The ROC analysis yield the area under curve (AUC) of them was 0.967 (P = 0.037), 0.923 (P = 0.048) , 0.981 (P = 0.034) , 0.981 (P = 0.034), respectively.
CONCLUSION: If the neurogenic tumors of soft tissue in the extremities had one or several features of these characteristics (irregular margin, big volume, edem around masses, aggressive behavior with adjoining fascia) on 3.0T MRI, they had more possibility to be malignant. T(2)-weighted fat suppression series on 3.0TMRI was very important for discrimination of tumor histological characteristics.

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Year:  2014        PMID: 24731456

Source DB:  PubMed          Journal:  Zhonghua Yi Xue Za Zhi        ISSN: 0376-2491


  1 in total

1.  Aggressive fibromatosis of the leg and sacrococcygeal region: a report of two cases.

Authors:  Fuwen Pan; Qiang Liu; Guoru Zhang; Qiqi Wang; Bo Yun; Yaoguang Han; Rui Deng; Linqing Wu; Shihua Wang
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01
  1 in total

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