A Rare Variant of Mazabraud’s Syndrome Overlapping with McCune-Albright Syndrome with a Clinical Review: A Case Report

D. Lee, S. Kwak, S. Jang, Hwanjun Choi, Jun Hyuk Kim
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Abstract

Mazabraud syndrome (MS) is a rare and sporadic disorder. It is mainly characterized by fibrous dysplasia (FD) of single or multiple bones and intramuscular myxomas (IM). Data on the prevalence since it was first reported, clinical features, and prognosis are extremely scarce. We report a case of a 59-year-old woman with IM and polyostotic FD. She also had multiple cafe’-au-lait spots suggestive of McCune-Albright syndrome (MAS). On magnetic resonance imaging, there are masses with well-defined heterogeneous enhancement, accompanied by an inner cyst in the vastus lateralis muscle and femur. These radiological results are identical to those of FD. After surgical intervention with excision of intramuscular soft-tissue mass, a diagnosis of IM of MS was confirmed. Given that cafe’-au-lait spots also appeared, the patient was diagnosed with a variant of MS with some of the clinical characteristics of MAS.
一罕见的马扎布罗氏综合征与麦库恩-奥尔布赖特综合征重叠的变异与临床回顾:一个病例报告
马扎布罗综合征(MS)是一种罕见的散发性疾病。主要表现为单骨或多骨纤维发育不良(FD)和肌内黏液瘤(IM)。自首次报道以来,有关该病的患病率、临床特征和预后的数据极为缺乏。我们报告一例59岁女性IM和多囊性FD。她身上还有多处咖啡斑,提示她患有麦丘内-奥尔布赖特综合征(MAS)。在磁共振成像上,有明确的不均匀强化肿块,并伴有股外侧肌和股骨内囊肿。这些放射学结果与FD相同。手术切除肌内软组织肿块后,确诊为多发性硬化症。考虑到还出现了咖啡斑,该患者被诊断为多发性硬化症的变体,具有多发性硬化症的一些临床特征。
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