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迟发性腺苷脱氨酶缺乏症表现为赫克病。

Late-onset adenosine deaminase deficiency presenting with Heck's disease.

机构信息

Department of Pediatric Immunology and Allergy, Meram Medical Faculty, Selcuk University, Beysehir yolu, 42080 Konya, Turkey.

出版信息

Eur J Pediatr. 2010 Aug;169(8):1033-6. doi: 10.1007/s00431-009-1131-9. Epub 2009 Dec 29.

Abstract

Focal epithelial hyperplasia, also known as Heck's disease, is a rare but distinctive entity of viral etiology with characteristic clinical and histopathological features. It is a benign, asymptomatic disease of the oral mucosa caused by human papilloma viruses (HPV). Previous studies postulated an association between these lesions and immunodeficiency. Genetic deficiency of adenosine deaminase (ADA) results in varying degrees of immunodeficiency, including neonatal onset severe combined immunodeficiency (ADA-SCID), and milder, later onset immunodeficiency. We report a 12-year-old girl with the late onset-ADA deficiency presenting with Heck's disease. Our case report should draw attention to the possibility of immunodeficiency in patients with HPV-induced focal epithelial hyperplasia.

摘要

局灶性上皮增生,又称 Heck 病,是一种罕见但具有特征性的病毒病因疾病,具有独特的临床和组织病理学特征。它是一种由人乳头瘤病毒(HPV)引起的口腔黏膜良性、无症状疾病。先前的研究推测这些病变与免疫缺陷有关。腺苷脱氨酶(ADA)的遗传缺陷导致不同程度的免疫缺陷,包括新生儿期严重联合免疫缺陷(ADA-SCID)和较轻的、较晚发病的免疫缺陷。我们报告了一例 12 岁女孩,患有晚发性 ADA 缺乏症,表现为 Heck 病。我们的病例报告应引起人们对 HPV 诱导的局灶性上皮增生患者发生免疫缺陷的可能性的关注。

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