Ghiringhelli P, Farfaglia P, Ghiringhelli L
Ospedale Provinciale di Gallarate, Divisione di Medicina I.
Minerva Med. 1987 Oct 31;78(20):1495-517.
Porphyrin metabolism disorders are grouped into three classes. 1) Hereditary porphyrias including those caused by an inherited deficiency in one of the enzymes responsible for porphyrin synthesis. 2) Secondary porphyrias: well defined clinical situations due to disturbed porphyrin metabolism caused by a variety of toxic substances or drugs or secondary to other pathological conditions. 3) porphyrin metabolism disorders as concomitant featured of certain types of poisoning or particular pathologies. This is followed by a brief description of porphyrin synthesis and the enzymes involved in it, and the distribution of porphyrins and their precursors in certain tissues and biological materials. Hereditary porphyrins are treated individually and not classified since all the classification systems proposed are open to criticism. However the value of grouping acute intermittent porphyria, hereditary coproporphyria, variegated porphyria and the porphyria caused by PBG-synthetase deficiency under "acute porphyrias" is recognised since all involve acute attacks with similar symptoms and prognoses, all are triggered by the same factors and all are treated in the same way. The various forms of hereditary porphyrias are grouped into 3 main categories: a) acute attacks featuring abdominal colics and signs of distress on the cerebral and peripheral nervous systems; b) skin alteration due to photosensitisation; c) haemolytic anaemia. Treatment is divided into preventive, symptomatic and aetiopathogenic. The individual hereditary porphyrias are then examined. The secondary porphyrias examined include lead poisoning, porphyria of the skin caused by hexachlorobenzene, subacute or chronic tyrosinaemia and acute intermittent porphyria caused by carbamazepine. Finally the porphyrin metabolism disorders concomitant with other diseases are examined including those encountered in anaemia, liver disease, dermatological conditions and infections and conditions caused by drugs and toxic substances.
卟啉代谢紊乱可分为三类。1)遗传性卟啉病,包括由卟啉合成所负责的一种酶的遗传性缺乏引起的疾病。2)继发性卟啉病:由各种有毒物质或药物引起的卟啉代谢紊乱,或继发于其他病理状况的明确临床情况。3)作为某些类型中毒或特定病理伴随特征的卟啉代谢紊乱。接下来简要描述卟啉合成及其相关酶,以及卟啉及其前体在某些组织和生物材料中的分布。遗传性卟啉病是单独治疗而不进行分类,因为所有提出的分类系统都受到批评。然而,将急性间歇性卟啉病、遗传性粪卟啉病、混合型卟啉病和由卟胆原合成酶缺乏引起的卟啉病归为“急性卟啉病”是被认可的,因为它们都涉及具有相似症状和预后的急性发作,都由相同因素触发且治疗方式相同。各种形式的遗传性卟啉病主要分为三大类:a)以腹部绞痛以及脑和周围神经系统的不适症状为特征的急性发作;b)由于光敏感引起皮肤改变;c)溶血性贫血。治疗分为预防性、对症性和病因性治疗。然后对各个遗传性卟啉病进行研究。所研究的继发性卟啉病包括铅中毒、六氯苯引起的皮肤卟啉病、亚急性或慢性酪氨酸血症以及卡马西平引起的急性间歇性卟啉病。最后研究与其他疾病伴随的卟啉代谢紊乱,包括在贫血、肝病、皮肤病学状况和感染以及由药物和有毒物质引起的状况中所遇到的情况。