Winship I M, Saxe N P, Hugel H
Department of Genetics, University of Cape Town, South Africa.
Clin Exp Dermatol. 1991 Sep;16(5):367-70. doi: 10.1111/j.1365-2230.1991.tb00403.x.
A young woman presented with renal failure and skin lesions of livedo reticularis (LR) due to primary oxalosis. Primary oxalosis is a rare autosomal-recessive error of metabolism characterized by accumulation of calcium-oxalate crystals in the kidneys, eyes, heart and skin. This unusual cause of intravascular obstruction resulting in livedo reticularis should be considered in patients with renal impairment. An approach to the diagnosis of LR is presented.
一名年轻女性因原发性草酸盐沉积症出现肾衰竭和网状青斑（LR）皮肤病变。原发性草酸盐沉积症是一种罕见的常染色体隐性代谢紊乱疾病，其特征是草酸钙晶体在肾脏、眼睛、心脏和皮肤中积聚。对于肾功能损害患者，应考虑这种导致网状青斑的血管内阻塞的不寻常病因。本文介绍了一种诊断网状青斑的方法。
