Stavros Kara, Motiwala Rajeev, Zhou Lan, Sejdiu Fatmir, Shin Susan
Department of Neurology, Mount Sinai School of Medicine, New York, NY.
J Clin Neuromuscul Dis. 2014 Mar;15(3):108-11. doi: 10.1097/CND.0000000000000024.
Calciphylaxis is a rare condition seen mostly in patients with chronic renal disease and secondary hyperparathyroidism who develop painful skin lesions and myopathy secondary to extensive small vessel calcification, which leads to tissue ischemia. It is typically diagnosed by a biopsy of prominent skin lesions. Here, we report a 49-year-old man with end-stage renal disease on chronic peritoneal dialysis who presented with weakness, myalgias, and necrotic skin lesions. Multiple skin biopsies were nondiagnostic because of severe extensive necrosis, and the diagnosis of systemic calciphylaxis was eventually made by a muscle biopsy. This case demonstrates the significant muscle involvement in calciphylaxis and highlights the importance of maintaining a high clinical suspicion for patients with risk factors for calciphylaxis, even when skin biopsy does not confirm it.
钙过敏是一种罕见病症,多见于患有慢性肾病和继发性甲状旁腺功能亢进的患者,这些患者会因广泛的小血管钙化继发疼痛性皮肤病变和肌病,进而导致组织缺血。通常通过对明显的皮肤病变进行活检来诊断。在此,我们报告一名49岁的终末期肾病患者,其接受慢性腹膜透析,出现了肌无力、肌痛和坏死性皮肤病变。由于严重的广泛坏死,多次皮肤活检均未得出诊断结果,最终通过肌肉活检确诊为系统性钙过敏。该病例表明钙过敏会显著累及肌肉,并强调对于有钙过敏风险因素的患者,即使皮肤活检未证实,也需高度临床怀疑的重要性。