Dvilansky A, Yermiahu T, Hatskelzon L
Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Sangre (Barc). 1992 Apr;37(2):133-5.
A 24-year-old Beduin pregnant woman in her 22nd week of gestation was treated successfully by plasmaphereses and steroids as soon as the diagnosis of TTP was confirmed by the clinical and laboratory criteria needed. Her sister died due to complications of TTP in pregnancy five years earlier while her other sister recuperated from TTP during pregnancy. However, fetal loss ensued. Thus, family history in pregnant women presenting with toxemia of pregnancy--like--syndrome may be the first clue to familial TTP.
一名24岁处于妊娠22周的贝都因族孕妇，一旦根据所需的临床和实验室标准确诊为血栓性血小板减少性紫癜（TTP），就立即通过血浆置换和类固醇进行了成功治疗。她的姐姐在五年前因妊娠合并TTP并发症去世，而她的另一个姐姐在怀孕期间从TTP中康复，但随后发生了胎儿丢失。因此，出现类似妊娠中毒症综合征的孕妇的家族史可能是家族性TTP的首要线索。
