Bernard Soulier Syndrome; A Rare Bleeding Disorder

P. Tripathi, K. Karthika, H. Pati, S. Tyagi
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引用次数: 2

Abstract

Bleeding syndromes in the newborn are rare, but they may be life-threatening and demand immediate attention. Congenital bleeding disorders especially pose a diagnostic challenge to the clinician because of their rarity and the need to be differentiated from the other common causes of bleeding in children. We present a case of an infant presenting with bleeding symptoms early in his life (since 5 months of age) which was initially thought to be immune thrombocytopenic purpura (ITP) with low platelet count. No response to steroids and further evaluation by platelet aggregometry and flowcytometry led to the correct diagnosis – Bernard soulier syndrome(BSS). Though, there is no specific treatment available for this rare bleeding disorder, however it is imperative to have arrived at correct diagnosis in order to save unnecessary therapy and to take due precautions for prevention of bleeding.
Bernard Soulier综合征;一种罕见的出血性疾病
新生儿出血综合征是罕见的,但它们可能危及生命,需要立即注意。先天性出血性疾病尤其对临床医生提出了诊断挑战,因为它们罕见,需要与其他常见的儿童出血原因区分开来。我们提出一例婴儿在他的生命早期出现出血症状(自5个月大),最初被认为是血小板计数低的免疫性血小板减少性紫癜(ITP)。对类固醇无反应,进一步的血小板聚集和流式细胞术评估导致正确的诊断-伯纳德·苏氏综合征(BSS)。虽然,对于这种罕见的出血性疾病没有特定的治疗方法,但是为了避免不必要的治疗和采取适当的预防措施来预防出血,必须做出正确的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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