Pimstone N R
Department of Internal Medicine, University of California, Davis, Sacramento.
Clin Dermatol. 1985 Apr-Jun;3(2):83-102. doi: 10.1016/0738-081x(85)90035-5.
This chapter has dealt with five photocutaneous forms of human porphyria. The forms are a diverse group of disorders with many different hematologic, hepatologic, and neurologic manifestations. In essence, most photocutaneous porphyrias occurring in childhood will relate to congenital erythropoietic porphyria or protoporphyria. The nature of the skin lesions and a study of the heme precursor profile in red cells, plasma, urine, and feces should easily distinguish these two conditions. CEP is a disease wherein photomutilation is a dominant concern and aggressive new approaches of therapy also have been discussed. In protoporphyria, the dermatologic problem is less severe and the dermatologist should be aware that a subset of patients could develop active liver disease that may lead to fatal cirrhosis. Novel approaches of therapy have been briefly alluded to. With regard to postpubertal photocutaneous porphyria, the classic porphyria cutanea tarda syndrome is associated with liver disease, usually alcoholic with siderosis, and the treatment by phlebotomy to reduce hepatic iron is highly effective. The potential danger of liver carcinoma has been discussed. In subsets of porphyria cutanea tarda, this can be an endemic disease relating to environmental factors, ie, ingestion of polyhalogenated hydrocarbons. The biochemical diagnosis can be attained by fairly straight-forward solvent extraction analyses of urine and feces, showing the dominance of uroporphyrin excretion in the urine and coproporphyrin in the feces. Chromatographic techniques in plasma, bile, and feces reveal a PCT-specific porphyrin: isocoproporphyrin. Rare subtypes with hematologic manifestations, ie, hepatoerythropoietic porphyria and CEP, indicate the wide spectra of disorders that might be associated with a spontaneous deficiency of uroporphyrinogen decarboxylase activity. These latter syndromes are, however, rare. Two hereditary hepatic porphyrias, ie, autosomal dominantly inherited VP and HCP, have been briefly discussed. The hepatic lesion is metabolic, not morphologic, and its expression by the liver relates to its adaptive response to induction of microsomal hemoproteins by a variety of exogeneous and endogeneous compounds, eg, drugs and hormones. Photocutaneous lesions of HCP and VP are identical to PCT, the latter having no neurologic sequelae. In the former two, however, exposure of persons to drugs, such as the hydantoins and barbiturates, can lead to potentially fatal acute porphyric attacks.(ABSTRACT TRUNCATED AT 400 WORDS)
本章探讨了人类卟啉病的五种光皮肤型。这些类型是一组多样的病症,具有许多不同的血液学、肝脏学和神经学表现。本质上,大多数儿童期发生的光皮肤型卟啉病与先天性红细胞生成性卟啉病或原卟啉病有关。皮肤病变的性质以及对红细胞、血浆、尿液和粪便中血红素前体谱的研究应能轻松区分这两种情况。先天性红细胞生成性卟啉病是一种以光致伤残为主要问题的疾病,同时也讨论了积极的新治疗方法。在原卟啉病中,皮肤病问题不太严重,皮肤科医生应意识到一部分患者可能会发展为活动性肝病,这可能导致致命的肝硬化。文中简要提及了新的治疗方法。关于青春期后光皮肤型卟啉病,经典的迟发性皮肤卟啉病综合征与肝病相关,通常是酒精性肝病伴铁沉积,通过放血疗法减少肝脏铁含量的治疗非常有效。文中讨论了肝癌的潜在风险。在迟发性皮肤卟啉病的某些亚型中,这可能是一种与环境因素有关的地方病,即摄入多卤代烃。通过对尿液和粪便进行相当简单的溶剂萃取分析即可实现生化诊断,结果显示尿液中尿卟啉排泄占主导,粪便中粪卟啉占主导。血浆、胆汁和粪便中的色谱技术揭示了迟发性皮肤卟啉病特有的卟啉:异粪卟啉。具有血液学表现的罕见亚型,即肝红细胞生成性卟啉病和先天性红细胞生成性卟啉病,表明可能与尿卟啉原脱羧酶活性自发缺乏相关的疾病谱很广。然而,后两种综合征很罕见。文中简要讨论了两种遗传性肝脏卟啉病,即常染色体显性遗传的变异型卟啉病和遗传性粪卟啉病。肝脏病变是代谢性的,而非形态学的,其在肝脏中的表现与肝脏对多种外源性和内源性化合物(如药物和激素)诱导微粒体血红素蛋白的适应性反应有关。遗传性粪卟啉病和变异型卟啉病的光皮肤病变与迟发性皮肤卟啉病相同,后者没有神经学后遗症。然而,在前两种疾病中,患者接触某些药物(如乙内酰脲类和巴比妥类药物)可能会引发潜在致命的急性卟啉病发作。(摘要截取自400字)