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重症新生儿先天性红细胞生成性卟啉病

Severe neonatal congenital erythropoietic porphyria.

作者信息

Hogeling Marcia, Nakano Taizo, Dvorak Christopher C, Maguiness Sheilagh, Frieden Ilona J

机构信息

Department of Dermatology, University of California, San Francisco, California, USA.

出版信息

Pediatr Dermatol. 2011 Jul-Aug;28(4):416-20. doi: 10.1111/j.1525-1470.2010.01376.x. Epub 2011 Mar 1.

Abstract

Congenital erythropoietic porphyria is a rare form of porphyria, presenting during the neonatal period or during infancy. Clinical features include photosensitive blistering and severe anemia. Wood's lamp fluorescence of the diaper is a useful screening test. We describe a severely affected neonate with systemic involvement due to a homozygous mutation. Because of ongoing severe hemolytic anemia and severe photosensitivity, bone-marrow transplantation was performed, but the patient ultimately succumbed to chemotherapy-induced lung damage, as well as severe pulmonary hypertension, likely due to his chronic hemolytic anemia.

摘要

先天性红细胞生成性卟啉病是一种罕见的卟啉病,在新生儿期或婴儿期发病。临床特征包括光敏性水疱和严重贫血。尿布的伍德灯荧光检查是一种有用的筛查试验。我们描述了一名因纯合突变而全身受累的重症新生儿。由于持续的严重溶血性贫血和严重光敏性,进行了骨髓移植,但患者最终死于化疗引起的肺损伤以及严重的肺动脉高压,这可能是由于他的慢性溶血性贫血所致。

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