妊娠期血栓性血小板减少性紫癜的成功治疗:1例报告

E. Naghshineh, M. Mostaghaci
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摘要

孕妇28岁,孕周24周,因前日积点及紫癜就诊,无外伤。从昨晚开始她就有枕部头痛。口腔及皮肤可见明显的点状及紫癜性病变。无肝脾肿大及淋巴结病变。她神志清醒,有方向感。患者发热、贫血、血小板减少,生命体征稳定。所有肝酶均升高。凝血指标正常。白细胞正常。红细胞减少,她有色素沉着症。可见明显的淋巴细胞增多。血小板明显减少。首次诊断为TTP。所有必要的实验室检查均已完成,以排除继发性TTP的风湿病原因;这些都是正常的。库姆斯试验呈阴性ADAMTS 13ab升高。胎儿超声检查正常。治疗开始于血浆置换和皮质类固醇。治疗后,血小板计数开始升高,LDH下降。病人出院时一般情况良好,实验室检查正常。她继续怀孕直到足月,生了一个正常的婴儿,没有任何并发症。直到2014年9月,她才出现TTP复发。
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Successful treatment of thrombotic thrombocytopenic purpura during pregnancy: A case report
A 28 years’ pregnant woman with 24 weeks’ gestational age referred with petechiae and purpura from previous day without any trauma. She had an occipital headache from last night. Overt petechial and purpuric lesions were seen in the mouth and skin. There was neither hepatosplenomegaly nor lymphadenopathy. She was conscious and oriented. The patient was febrile, anemic and thrombocytopenic with stable vital signs. All liver enzymes were elevated. Coagulation profile was normal. WBCs were normal. RBCs were reduced, and she had polychromatosis. Overt shistocytosis was seen. Platelets were significantly decreased. The first diagnosis was TTP. All necessary laboratory tests were done to rule out the secondary rheumatologic causes of TTP; which all were normal. Coombs tests were negative. ADAMTS 13 Ab was elevated. Fetal ultrasonography was normal. Treatment started with plasmapheresis and corticosteroid. After treatment, platelets count begins elevated, and LDH decreased. The patient discharged with a good general condition and normal lab tests. She continued her pregnancy until term, and born a normal infant without any complication. She did not have a recurrence of TTP until September 2014.
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