A Giant Enchondroma Mimicking Sarcoidosis: Report of Case and Review of the Literature

A. Atik, Koray Ba delio lu, N. Şahin, S. Sargin
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Abstract

Sarcoidosis of the humerus is exceptionally rare and only a few cases have been reported. In this mini-review, a case of enchondroma in proximal humerus mimicking sarcoidosis and the features of bone involvement of sarcoidosis were reviewed. A 41-year-old female who was diagnosed with sarcoidosis in 2009 had used corticosteroids for 4 months. She had not any symptoms until 2014. She was admitted the clinic with a 2-month-history of erythema nodosum on her legs and right shoulder pain. Values of laboratory tests were all within normal limits except erythrocyte sedimentation rate and C-reactive protein levels. The mass in the proximal metaphyseal humerus has the characteristic as a medullary lesion which had calcifications in CT sections. MR images that the mass had low signal intensity on T1-weighted images and heterogeneous high signal intensity on T2-weighted images. It had irregular nodular contrast and the mass did not cause the expansion of the bone. Increased activity was observed on scintigraphy. We suspected the mass which was realized incidentally in a patient with sarcoidosis, could be bone sarcoidosis. As a result of our biopsy, it was enchondroma. Bone neoplasms should be kept in mind in issues like our case report.
一个巨大的模拟结节病的内生纤维瘤:病例报告及文献复习
肱骨结节病极为罕见,仅有少数病例被报道。在这个小型的回顾,在肱骨近端模拟结节病的内生纤维瘤和结节病累及骨的特点进行了回顾。一位41岁女性于2009年被诊断为结节病,已使用皮质类固醇4个月。她直到2014年才出现任何症状。患者因2个月的腿部结节性红斑和右肩疼痛入院。除血沉、c反应蛋白水平外,实验室各项指标均在正常范围内。肱骨干骺端肿块在CT切片上表现为髓样病变并有钙化。MR图像显示肿块在t1加权图像上呈低信号强度,在t2加权图像上呈异质性高信号强度。它有不规则的结节状对比,肿块没有引起骨扩张。在闪烁图上观察到活性增加。我们怀疑结节病患者偶然发现的肿块可能是骨结节病。根据我们的活组织检查,这是内生纤维瘤。在我们的病例报告中,骨肿瘤应该被牢记。
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