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累及锁骨的孤立性婴儿肌纤维瘤病

Solitary infantile myofibromatosis involving the clavicle.

作者信息

Imaizumi S, Ogose A, Hotta T, Takahashi H E, Emura I

机构信息

Department of Orthopedic Surgery, Niigata University School of Medicine, Asahimachidouri 1-757 Niigata City, Niigata, Japan 951-8510, USA.

出版信息

Skeletal Radiol. 1999 Aug;28(8):473-6. doi: 10.1007/s002560050550.

Abstract

A rare case of solitary infantile myofibromatosis of bone is reported in the right clavicle of a 15-year-old boy. A radiograph demonstrated an osteolytic lesion with a sharp margin and a sclerotic rim. CT revealed a circumscribed lesion with slight expansion of the cortex. On MRI the lesion appeared isointense to muscle on T1-weighted images, bright on T2-weighted images, and showed marked gadolinium enhancement. The patient was well, without evidence of recurrence or metastasis, 4 years and 5 months following resection.

摘要

报告了一例罕见的发生于一名15岁男孩右锁骨的孤立性骨婴儿肌纤维瘤病。X线片显示为一个边缘清晰且有硬化边缘的溶骨性病变。CT显示为一个边界清楚且皮质有轻度膨胀的病变。在MRI上,该病变在T1加权像上与肌肉信号等强,在T2加权像上呈高信号,并显示出明显的钆强化。切除术后4年零5个月,患者情况良好,无复发或转移迹象。

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