[Thrombotic thrombocytopenic purpura: report of seven cases].

Elisa Anselmi, Annalisa Arcari, Patrizia Bernuzzi, Giuseppe Civardi, Carlo Filippo Moroni, Daniele Vallisa, Raffaella Bertè, Antonio Lazzaro, Luigi Cavanna
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Abstract

From May 1999 to January 2002 we observed 7 patients (4 females and 3 males, median age 55 years, range 31-81 years) with thrombotic thrombocytopenic purpura (TTP). Six patients has been previously undiagnosed and 1 patient was at second relapse. Trigger factors of TTP were identified in 6 patients: ticlopidine treatment (2 patients); an acute cutaneous infection episode immediately before the features of TTP (1 patient); presence of devices: orthodontic (1 patient) and intrauterine contraceptive (1 patient), Mycoplasma urealyticum vaginal infection (1 patient). In all the 7 patients the clinical status was mainly related to the hemolytic anemia, thrombocytopenia and neurological events. One of these patients presented with hemolytic-uremic syndrome with acute renal failure and macrohematuria at onset, another one showed a systemic exanthema post-infection-like. Six out of 7 patients presented with different neurological events: headache, confusion, focal neurological failure. All the 7 patients were promptly treated with plasma-exchange and cryosupernatant plasma infusion. In addition they received prednisone 25-50 mg/day. All the 7 patients achieved a complete remission after plasma-exchange, one relapsed 3 months later and was treated with plasma-exchange again. All the patients are in complete remission with a median follow-up of 36.3 months (range 20-62 months). From these cases we suggest: 1) clinicians should take in mind the suspicion of TTP in every patient with hemolytic, negative direct Coombs test, anemia, thrombocytopenia, high level of lactate dehydrogenase; 2) the treatment of choice is plasma-exchange; 3) the response of treatment is good if therapy is promptly and aggressively administered; 4) the possible role of a trigger factor for removing it and to prevent relapses.

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血栓性血小板减少性紫癜7例报告
自1999年5月至2002年1月,我们观察到7例血栓性血小板减少性紫癜(TTP),其中女4例,男3例,中位年龄55岁,年龄范围31 ~ 81岁。6例既往未确诊,1例二次复发。6例患者中TTP的触发因素:噻氯匹定治疗(2例);在出现TTP症状之前,有一次急性皮肤感染发作(1例);存在器械:正畸(1例)和宫内避孕(1例),解脲支原体阴道感染(1例)。7例患者的临床状况主要与溶血性贫血、血小板减少和神经系统事件有关。其中1例患者在发病时表现为溶血性尿毒症综合征伴急性肾功能衰竭和大量血尿,另1例患者表现为感染后全身性皮疹样。7例患者中有6例出现不同的神经系统事件:头痛、意识模糊、局灶性神经功能衰竭。7例患者均及时行血浆置换和低温上清血浆输注治疗。此外,他们接受强的松25-50毫克/天。7例患者经血浆置换后均完全缓解,1例3个月后复发,再次行血浆置换治疗。所有患者均完全缓解,中位随访36.3个月(范围20-62个月)。根据这些病例,我们建议:1)临床医生对溶血、直接库姆斯试验阴性、贫血、血小板减少、乳酸脱氢酶高水平的患者应注意TTP的怀疑;2)治疗方式选择血浆置换;3)如果治疗及时且积极,治疗效果良好;4)可能的触发因素的作用,以消除它,防止复发。
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