炎性肌纤维母细胞瘤的影像表现与病理研究

Imaging Manifestations and Pathological Study of Inflammatory Myofibroblastoma

目的:分析炎性肌纤维母细胞瘤的影像表现与病理研究。方法:回顾性分析2013年1月-2020年1月我院手术治疗的10例确诊的炎性肌纤维母细胞瘤患者的CT、MRI影响表现及病理检查结果。结果:10例患者中,2例病灶于胃部,2例病灶于肺部,1例病灶为腹腔,1例病灶为大腿软组织,2例病灶为肠系膜,1例病灶为输尿管,1例病灶为腹部。8例为单发病灶,2例为多发病灶,其中3例因粘性变成囊实性,另外7例仅有一例患者出现钙化。结论:炎性肌纤维母细胞瘤是临床较为少见的肿瘤,采用影像诊断能够帮助临床医师对患者病灶部位进行定位,观察患者的病情发展情况,但仍需要病理检查进行进一步的确诊。

Objective:To analyze the imaging manifestations and pathological studies of inflammatory myofibroblastoma.Methods:Retrospective analysis of CT,MRI and pathological findings of 10 patients with inflammatory myofibroblastoma who were surgically treated in our hospital from January 2013 to January 2020.Results:Of the 10 patients,2 cases were in the stomach,2 cases were in the lungs,1 case was the abdominal cavity,1 case was the soft tissue of the thigh,2 cases were the mesentery,1 case was the ureter,1 case was the lesion abdomen.8 cases were single lesions,2 cases were multiple lesions,of which 3 cases became cystic and solid due to stickiness,and only one patient had calcification in the other 7 cases.Conclusion:Inflammatory myofibroblastoma is a rare tumor in clinical practice.Imaging diagnosis can help clinicians locate the patient’s lesion and observe the patient’s disease development.However,pathological examination is still needed for further diagnosis.