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暴发性肌肉骨骼和神经结节病:病例报告及文献综述

Fulminant musculoskeletal and neurologic sarcoidosis: case report and literature update.

作者信息

Sweeney Ashley, Hammer Richard, Evenski Andrea, Crim Julia

机构信息

University of Missouri at Columbia, Columbia, MO, USA.

出版信息

Skeletal Radiol. 2016 Nov;45(11):1571-6. doi: 10.1007/s00256-016-2463-y. Epub 2016 Sep 5.

Abstract

We report a case of fulminant sarcoidosis in a 28-year-old man presenting with skin nodules, multifocal small and large joint arthralgias, and blurred vision. Characteristic bone, soft tissue, articular, and CNS findings were evident on multimodality imaging. Bony abnormalities included near-complete destruction of a distal phalanx, "lace-like" lucent lesions, erosive arthritis, lytic lesions with and without sclerotic margins, and bone marrow replacement visible only on MRI. The extent of bony disease at time of presentation was unusual. We review the widely varying reported prevalence of imaging findings of bony sarcoidosis in the literature, and discuss reasons for this variability. We found that musculoskeletal findings at US and MRI were less specific than radiographic and CT findings, but were useful in quantifying extent of disease.

摘要

我们报告一例28岁男性暴发性结节病,患者表现为皮肤结节、多灶性大小关节疼痛和视力模糊。多模态影像学检查显示出特征性的骨骼、软组织、关节和中枢神经系统表现。骨骼异常包括远端指骨几乎完全破坏、“花边样”透亮区、侵蚀性关节炎、有或无硬化边缘的溶骨性病变,以及仅在磁共振成像(MRI)上可见的骨髓替代。就诊时骨骼疾病的范围并不常见。我们回顾了文献中报道的骨结节病影像学表现的广泛差异患病率,并讨论了这种变异性的原因。我们发现,超声和MRI的肌肉骨骼表现不如X线和CT表现特异,但有助于量化疾病范围。

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