Regular review: Diagnosis and management of porphyria

作者：H. Thadani · 发表于：BMJ · 年份：2000 · DOI：10.1136/bmj.320.7250.1647 · 被引用次数：185 · 研究领域：Porphyrin Metabolism and Disorders、Heme Oxygenase-1 and Carbon Monoxide、Methemoglobinemia and Tumor Lysis Syndrome

Although porphyria is a relatively uncommon condition, it should be considered in patients presenting with an atypical medical, psychiatric, or surgical history. Acute attacks are associated with a substantial morbidity and mortality; there is a need for rapid and accurate diagnosis of the neuropsychiatric porphyrias, particularly because haem arginate can induce a definite remission if given early in an attack. Additionally, porphyrias may present with skin lesions or photosensitivity. #### Summary points The porphyrias form a group of inherited disorders of haem biosynthesis of which there are seven main types Porphyrias can be classified into acute (neuropsychiatric), cutaneous, and mixed forms Acute forms can be life threatening, but attacks can be aborted by early administration of haem arginate The acute porphyrias are often misdiagnosed; most commonly they present as acute abdominal pain or as neurological or atypical psychiatric symptoms Patients with porphyria should be referred to specialist centres and be advised to avoid precipitating factors, such as certain drugs When a patient is diagnosed with an acute porphyria the whole family needs to be screened The porphyrias form a heterogeneous group of inherited disorders of haem biosynthesis, and they are often missed or wrongly diagnosed. A partial deficiency of one of the seven enzymes in the pathway causes characteristic clinical and biochemical features. These disorders are due to a specific alteration in ...