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光敏患者中卟啉病的检测。

The detection of porphyria in photosensitive patients.

作者信息

Rossi E, Curnow D H, Schenberg H

出版信息

Pathology. 1978 Jan;10(1):17-26. doi: 10.3109/00313027809063476.

Abstract

The biochemical diversity of the various porphyris often leads to incomplete investigation of photosensitive patients and porphyria may be excluded wrongly on the basis of normal urinary porphyrins alone. Establishing a biochemical referral centre for photosensitive patients suspected of having porphyria led to the diagnosis of 5 cases of porphyria cutanea tarda (PCT) and 2 cases of erythropoietic protoporphyria (EPP) among 34 patients referred by dermatologists over a period of 12 months. Iron overload was conformed in 3 the PCT patients by plasma ferritin assay. Studies on the available families of the two EPP patients revealed elevated red cell protoporphyrin levels in several clinically asymptomatic relatives.

摘要

各种卟啉的生化多样性常常导致对光敏患者的调查不完整,卟啉病可能仅基于正常的尿卟啉就被错误地排除。为疑似患有卟啉病的光敏患者建立生化转诊中心后,在皮肤科医生转诊的34例患者中,在12个月内诊断出5例迟发性皮肤卟啉病(PCT)和2例红细胞生成性原卟啉病(EPP)。通过血浆铁蛋白测定,3例PCT患者确诊存在铁过载。对两名EPP患者的现有家族进行的研究显示,几名临床无症状的亲属红细胞原卟啉水平升高。

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