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呈加速期表现的切-希二氏综合征

Chediak-Higashi syndrome presenting in accelerated phase.

作者信息

Imran Tanzeel, Zafar Lubna, Rehan Madeeha, Nasir Aqsa, Tariq Parveen Akhtar, Batool Iffat

机构信息

Department of Haematology, Fauji Foundation Hospital, Jehlum Road, Rawalpindi.

出版信息

J Coll Physicians Surg Pak. 2012 Aug;22(8):539-41.

Abstract

Chediak-Higashi Syndrome (CHS) is a rare autosomal recessive disorder, characterized by silver hair, recurrent infections, partial oculo-cutaneous albinism, mild coagulation defect and progressive neuropathy. The characteristic feature of CHS is the presence of huge lysosomes and cytoplasmic inclusions within different body cells like the white blood cells. The disease has an early onset but usually presents in an accelerated phase. We present a case of a 2 years old boy with high grade fever, bilateral cervical lymphadenopathy, hepatosplenomegaly, abdominal distention of 28 days duration. He was diagnosed with Chediak-Higashi syndrome in accelerated phase on the basis of clinical presentation, morphological findings on peripheral blood film and bone marrow aspirate.

摘要

切迪阿克-希加希综合征(CHS)是一种罕见的常染色体隐性疾病,其特征为白发、反复感染、部分眼皮肤白化病、轻度凝血缺陷和进行性神经病变。CHS的特征性表现是在不同体细胞(如白细胞)内存在巨大的溶酶体和细胞质内含物。该疾病起病较早,但通常会进入加速期。我们报告一例2岁男孩,持续高热28天,伴有双侧颈部淋巴结肿大、肝脾肿大及腹胀。根据临床表现、外周血涂片和骨髓穿刺的形态学检查结果,他被诊断为处于加速期的切迪阿克-希加希综合征。

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