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Proteus 综合征:一例伴有骨骼闪烁显像结果的病例报告。

Proteus syndrome: a case report with bone scintigraphy findings.

机构信息

Department of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Diagn Interv Radiol. 2013 May-Jun;19(3):240-3. doi: 10.5152/dir.2013.081.

Abstract

Proteus syndrome is an extremely rare genetic disorder characterized by an asymmetrical overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. We present a case of a six-year-old boy with proteus syndrome who underwent bone scintigraphy for suspected osteomyelitis. Bone scintigraphy ruled out osteomyelitis and suggested cellulitis. In addition, it demonstrated striking characteristic deformities, which need to be emphasized. Knowledge of these findings will avoid misinterpretation of bone scintigraphy in patients with proteus syndrome.

摘要

脑颜面血管瘤病(Sturge-Weber 综合征)是一种罕见的神经皮肤综合征,其主要特征为软脑膜血管瘤、同侧面部三叉神经分布区的葡萄酒色斑、青光眼及对侧偏瘫。我们报道了 1 例以头痛为主要表现的脑颜面血管瘤病患者,头颅 CT 检查发现左侧顶枕叶脑梗死,磁共振血管成像(MRA)提示左侧大脑中动脉 M1 段重度狭窄,经积极治疗后头痛缓解。脑颜面血管瘤病患者的首发症状可为头痛,对于头痛伴葡萄酒色斑的患者,需警惕脑颜面血管瘤病的可能,建议行颅脑 CT 或磁共振检查以明确诊断。

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