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髂腰肌局灶性肌炎——一种良性假肿瘤:超声表现及其与CT和MRI的相关性

Focal myositis of the iliopsoas muscle--a benign pseudotumour: ultrasound appearance in correlation with CT and MRI.

作者信息

Hoffmann A, Buitrago Téllez C, Tolnay M, Tyndall A, Steinbrich W

机构信息

Department of Radiology, University Hospital Basel, Switzerland.

出版信息

Ultraschall Med. 2006 Apr;27(2):180-4. doi: 10.1055/s-2005-858371.

Abstract

OBJECTIVE

Focal myositis of the iliopsoas muscle is a rare condition. A case is presented, emphasizing the value of ultrasound for detection, localisation, image-guided biopsy and follow-up in correlation with CT and MRI findings.

MATERIAL AND METHODS

A 58-year-old woman was referred to our clinic with strong left sided inguinal pain, which radiated to the thigh and had lasted for four days. Ultrasound, CT and MRI were performed. Ultrasound-guided biopsy with histological correlation was obtained and US-follow-ups were available.

RESULTS

CT showed an enlarged iliopsoas muscle on the left side without any focal pathology or enhancement. MRI revealed a sharpely delineated lesion, which was hypointense to muscle in fat-suppressed T1 w images with circumferential enhancement and showed a hyperintense appearance in T2 w images. Ultrasound displayed a polylobulated, inhomogeneous and hypoechoic tumour within the iliopsoas muscle. Ultrasound-guided biopsy was found to be compatible with myositis. After oral therapy with steroids, improvement could be documented by serial ultrasound follow-up as the size of the tumour was definitely regressing.

CONCLUSION

Focal myositis of the iliopsoas muscle is a rare entity which may mimic a tumoural lesion. Imaging findings may not be conclusive, and US-guided biopsy is recommended to rule out a malignant mass. Ultrasound seems to be the most cost-effective method for diagnosis, image guided biopsy and follow-up.

摘要

目的

髂腰肌局灶性肌炎是一种罕见疾病。本文报告一例,强调超声在检测、定位、图像引导活检及随访方面的价值,并与CT和MRI结果进行对比。

材料与方法

一名58岁女性因左侧腹股沟剧烈疼痛前来我院就诊,疼痛放射至大腿,持续了四天。进行了超声、CT和MRI检查。获取了超声引导下的活检组织并进行组织学关联分析,且有超声随访结果。

结果

CT显示左侧髂腰肌增大,无任何局灶性病变或强化。MRI显示一个边界清晰的病变,在脂肪抑制T1加权图像上相对于肌肉呈低信号,有环形强化,在T2加权图像上呈高信号。超声显示髂腰肌内有一个多叶状、不均匀且低回声的肿瘤。超声引导下活检结果与肌炎相符。口服类固醇治疗后,通过系列超声随访可记录到病情改善,因为肿瘤大小明显缩小。

结论

髂腰肌局灶性肌炎是一种罕见病症,可能类似肿瘤性病变。影像学表现可能不具有决定性,建议进行超声引导下活检以排除恶性肿块。超声似乎是诊断、图像引导活检及随访最具成本效益的方法。

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