Jiménez López A, García Marcos M A, Cañizo Fernández-Roldán C, Fuertes Martín K, Hernández Vicente I, Pastor Encinas I
Med Clin (Barc). 1980 Jan 10;74(1):31-3.
A case of CRST syndrome associated with a type III mixed cryoglobulinemia according to Seligman's classification is presented. The authors stress the concrete individualization of this syndrome, as well as the importance of the Raynaud's phenomenon as the first and early manifestation in the clinical picture. They state, on the other hand, that the abundance and distribution of the telangiectasias is similar to the hereditary Rendu-Osler telangiectasia. Finally, a possible common physiopathologic basis for the syndrome and the associated cryoglobulinemia in this patient is suggested.
本文报告了一例根据塞利格曼分类法与III型混合性冷球蛋白血症相关的CRST综合征病例。作者强调了该综合征具体的个体化特征，以及雷诺现象作为临床表现中首发和早期表现的重要性。另一方面，他们指出毛细血管扩张的数量和分布与遗传性遗传性出血性毛细血管扩张症相似。最后，提出了该患者综合征与相关冷球蛋白血症可能的共同生理病理基础。
