Martin S
Arch Dermatol. 1979 Feb;115(2):208-11.
A patient with purpura, acral blisters, and ulcerations was evaluated and found to have cryofibrinogenemia and an IgG K light chain monoclonal gammopathy. No other systemic illness was found. The overall incidence of significant cryofibrinogenemia include neoplastic, thrombotic, infectious, and miscellaneous disorders. The patient described was not easily classified. This case is probably best considered primary or idiopathic cryofibrinogenemia.
对一名患有紫癜、肢端水疱和溃疡的患者进行了评估，发现其患有冷纤维蛋白原血症和IgG κ轻链单克隆丙种球蛋白病。未发现其他全身性疾病。显著冷纤维蛋白原血症的总体发病率包括肿瘤性、血栓性、感染性和其他杂类疾病。所描述的该患者不易分类。此病例可能最好被视为原发性或特发性冷纤维蛋白原血症。
