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先天性角化不良中的肺动静脉畸形

Pulmonary Arteriovenous Malformations in Dyskeratosis Congenita.

作者信息

Samuel Bennett P, Duffner Ulrich A, Abdel-Mageed Aly S, Vettukattil Joseph J

机构信息

Congenital Heart Center, Helen DeVos Children's Hospital of Spectrum Health, Grand Rapids, Michigan.

Blood and Bone Marrow Transplant, Helen DeVos Children's Hospital of Spectrum Health, Grand Rapids, Michigan.

出版信息

Pediatr Dermatol. 2015 Jul-Aug;32(4):e165-6. doi: 10.1111/pde.12589. Epub 2015 Apr 9.

Abstract

Pulmonary arteriovenous malformations (PAVMs) are rare lesions known to cause cyanosis due to abnormal communication between the pulmonary arteries and veins. They are commonly seen in association with hereditary hemorrhagic telangiectasia, congenital heart disease, hepatopulmonary syndrome, and portopulmonary shunting, but rarely in patients with dyskeratosis congenita (DC). We describe a patient previously diagnosed with DC confirmed to have microscopic PAVMs after bone marrow transplantation and discuss possible pathogenic mechanisms.

摘要

肺动静脉畸形(PAVM)是一种罕见的病变,已知由于肺动脉和静脉之间的异常连通而导致发绀。它们通常与遗传性出血性毛细血管扩张症、先天性心脏病、肝肺综合征和肺内分流相关,但在先天性角化不良(DC)患者中很少见。我们描述了一名先前被诊断为DC的患者,在骨髓移植后确诊患有微小PAVM,并讨论了可能的致病机制。

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