Rossi E, Curnow D H, Schenberg H
Pathology. 1978 Jan;10(1):17-26. doi: 10.3109/00313027809063476.
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.
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。