Ollier Disease With Digital Enchondromatosis Anatomic and Functional Imaging

被引：1

作者：

Le, Bryan B. ^{[1
]}

Nguyen, Ba D. ^{[1
]}

机构：

[1] Mayo Clin, Dept Radiol, Scottsdale, AZ 85259 USA

来源：

CLINICAL NUCLEAR MEDICINE | 2014年 / 39卷 / 08期

关键词：

Ollier disease; finger; PET; MRI; bone scintigraphy; radiographs; MAFFUCCI SYNDROME; HAND; CHONDROSARCOMA;

D O I：

10.1097/RLU.0000000000000284

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

Ollier disease is a rare skeletal disorder characterized by multiple enchondromas at metaphyseal regions of the bones. The disease is non-hereditary and usually the result of postzygote mutations during development. We present the features of digital enchondromatosis on bone scintigraphy, PET/CT, radiographs, and MRI in a patient, with a childhood diagnosis of Ollier disease.

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页码：E375 / E378

页数：4

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