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[血栓性血小板减少性紫癜:7例报告]

[Thrombotic thrombocytopenic purpura: report of seven cases].

作者信息

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

机构信息

Divisione di Medicina Oncologica ed Ematologia, Ospedale "Guglielmo da Saliceto" di Piacenza.

出版信息

Ann Ital Med Int. 2005 Apr-Jun;20(2):108-12.

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.

摘要

1999年5月至2002年1月,我们观察了7例血栓性血小板减少性紫癜(TTP)患者(4例女性,3例男性,中位年龄55岁,范围31 - 81岁)。6例患者此前未被诊断,1例患者为第二次复发。6例患者确定了TTP的触发因素:噻氯匹定治疗(2例);TTP症状出现前立即发生的急性皮肤感染发作(1例);存在器械:正畸器械(1例)和宫内节育器(1例),解脲脲原体阴道感染(1例)。所有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例患者起病时表现为溶血尿毒综合征伴急性肾衰竭和肉眼血尿,另1例表现为感染后样全身性皮疹。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、局灶性神经功能障碍。所有7例患者均立即接受了血浆置换和冷上清血浆输注治疗。此外,他们还接受了每日25 - 50毫克的泼尼松治疗。所有7例患者在血浆置换后均实现了完全缓解,1例在3个月后复发并再次接受血浆置换治疗。所有患者均处于完全缓解状态,中位随访时间为36.3个月(范围20 - 62个月)。从这些病例中我们建议:1)临床医生对于每一位有溶血、直接抗人球蛋白试验阴性、贫血、血小板减少、乳酸脱氢酶水平升高的患者都应考虑TTP的可能性;2)首选治疗方法是血浆置换;3)如果及时、积极地进行治疗,治疗反应良好;4)触发因素在去除及预防复发方面可能起作用。

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