Jefferson Institute of Molecular Medicine and Division of Connective Tissue Diseases, Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.
J Clin Rheumatol. 2011 Sep;17(6):318-22. doi: 10.1097/RHU.0b013e31822be61e.
Scleromyxedema is a systemic disease characterized by lichenoid papules, nodules, and plaques on the skin and often diffuse skin induration resembling the cutaneous involvement of systemic sclerosis. The systemic involvement affects the musculoskeletal, pulmonary, cardiovascular, gastrointestinal, and central nervous systems, and the disorder is commonly associated with a paraproteinemia. Involvement of the kidney is rare and not considered a feature of the disease. Here, we describe an unusual case of scleromyxedema complicated by the development of scleroderma renal crisis-like acute renal failure with a marked intimal deposition of mucin, mucopolysaccharides, and hyaluronic acid in the intrarenal vessels.
硬肿性黏液水肿是一种全身性疾病,其特征为皮肤出现苔藓样丘疹、结节和斑块,且常伴有弥漫性皮肤硬化,类似于系统性硬皮病的皮肤受累。全身性受累影响肌肉骨骼、肺、心血管、胃肠道和中枢神经系统,该疾病通常与副蛋白血症相关。肾脏受累罕见,不被认为是该疾病的特征。在此,我们描述了一例硬肿性黏液水肿的不典型病例,其并发了类似于硬皮病肾危象的急性肾衰竭,肾内血管有明显的内膜黏液、黏多糖和透明质酸沉积。