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Prolonged survival after splenectomy in Wiskott-Aldrich syndrome: a case report

机译:Wiskott-Aldrich综合征脾切除术后延长生存期:病例报告

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摘要

Wiskott-Aldrich syndrome is a rare X-linked immunodeficiency disorder that is characterized by a variable clinical phenotype. Matched donor bone marrow transplantation is currently the only curative therapeutic option. We present the case of a 24-year-old male who was diagnosed at the age of seven with Wiskott-Aldrich syndrome. He did not respond to intravenous gammaglobulin and he experienced recurrent pulmonary infections despite prophylactic antibiotics. The patient had no matched donor. At the age of nine, he was submitted to splenectomy and his platelet count was normalized. Fifteen years later, the patient remains asymptomatic with a normal platelet count. He is still receiving prophylactic antibiotics and no bleeding episodes or septic complications have been reported. This case demonstrates that splenectomy can represent a safe therapeutic option in selected WAS patients, provided that there is a tight follow-up program, patient education and adherence to guidelines regarding post-splenectomy prophylaxis.
机译:Wiskott-Aldrich综合征是一种罕见的X连锁免疫缺陷病,其特征是临床表型可变。匹配的供体骨髓移植目前是唯一的治疗选择。我们介绍了一名24岁男性,该男性在7岁时被诊断患有Wiskott-Aldrich综合征。他对静脉内的球蛋白无反应,尽管使用了预防性抗生素,但仍反复发生肺部感染。该患者没有匹配的供体。 9岁时,他接受了脾切除术,血小板计数恢复正常。十五年后,患者仍无症状,血小板计数正常。他仍在接受预防性抗生素治疗,没有出血事件或感染性并发症的报道。该病例表明,如果有严格的随访计划,患者教育并遵守有关脾切除术后预防的指导原则,则脾切除术可以代表某些WAS患者的安全治疗选择。

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