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Nonfamilial hyperphosphatemic tumoral calcinosis with ulnar neuropathy.

机译：非家族性高磷酸盐血症性肿瘤钙化伴尺神经病变。

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摘要

We present a case of multiple large juxta-articular painless masses involving both the elbows and right hip in a 27-year old south Asian male who presented with ulnar neuropathy and constitutional symptoms. Radiology, blood investigations and biopsy confirmed it to be hyperphosphatemic tumoral calcinosis. Patient was also diagnosed with an extremely rare association, testicular microlithiasis. Complete surgical excision with low phosphate diet resulted in complete neurological recovery and no recurrence at 30 months. Tumoral calcinosis should be considered in the differential diagnosis of a case with multiple, symptomatic juxta-articular masses.
机译：我们在一个27岁的南亚男性患者中出现了一个涉及肘部和右髋的多个大型近关节无痛性肿块的病例，该男性患者出现尺神经病和体质症状。放射学，血液检查和活检证实这是高磷酸盐血症性肿瘤性钙化病。患者还被诊断出患有极为罕见的睾丸微石症。低磷酸盐饮食的完全手术切除可导致神经功能完全恢复，并且在30个月内没有复发。鉴别诊断为多发性症状性并发关节假体的病例应考虑肿瘤性结石病。

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