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急性卟啉病:内科和急诊医学中的诊断与治疗挑战

The acute porphyrias: a diagnostic and therapeutic challenge in internal and emergency medicine.

作者信息

Ventura Paolo, Cappellini Maria Domenica, Rocchi Emilio

机构信息

Department of Medicines and Medical Specialties, Ambulatorio delle Porfirie e delle Malattie da Disturbo del Metabolismo degli Aminoacidi, University of Modena and Reggio Emilia, Policlinico of Modena, Largo del Pozzo 71, Modena, Italy.

出版信息

Intern Emerg Med. 2009 Aug;4(4):297-308. doi: 10.1007/s11739-009-0261-4. Epub 2009 May 29.

Abstract

The porphyrias are a heterogeneous group of metabolic diseases resulting from a variable catalytic defect of one of the eight enzymes involved in the heme biosynthesis pathway; they are mostly inherited diseases, but in some circumstances the metabolic disturbance may be acquired. The specific patterns of tissue overproduction (and hence accumulation and excretion) of toxic heme precursors, associated with each enzymatic deficiency, are responsible for the characteristic biochemical and clinical features of each of these diseases. Moreover, even in the presence of a specific inherited enzymatic defect, many different environmental factors (such as drugs, calorie restriction, hormones, sunlight exposition, infections, etc.) often play a key role in triggering the clinical expression of the various forms of porphyrias. The porphyrias are often misdiagnosed diseases, due their multiform clinical manifestations, able to mimic many other more common diseases. For this reason, many different specialists, such as surgeons, psychiatrists, gastroenterologists, neurologists, emergency physicians and dermatologists may be variably involved in the diagnostic process, especially for the forms presenting with acute and life-threatening clinical features. According to the clinical features, the porphyrias can be classified into neuropsychiatric (characterized by neurovisceral crises involving autonomic and central nervous system but also the liver and the kidney with possible consequences in terms of neurological, psychic, cardiac, respiratory, liver and kidney functions), dermatological (mostly presenting with cutaneous lesions due to photosensitivity), and mixed forms. From a strictly clinical point of view, porphyrias presenting with neurovisceral attacks are also referred as acute porphyrias: they are the object of the present review. An accurate diagnosis of acute porphyria requires knowledge and the use of correct diagnostic tools, and it is mandatory to provide a more appropriate therapeutic approach and prevent the use of potentially unsafe drugs, able to severely precipitate these diseases, especially in the presence of life-threatening symptoms. To date, availability of a relatively stable haem preparation (haem arginate) has significantly improved the treatment outcome of acute porphyric attacks, so the knowledge about the diagnosis and the management of these diseases may be relevant for physicians working in internal medicine, neurology and emergency units.

摘要

卟啉病是一组异质性代谢疾病,由血红素生物合成途径中八种酶之一的可变催化缺陷引起;它们大多是遗传性疾病,但在某些情况下,代谢紊乱可能是后天获得的。与每种酶缺乏相关的有毒血红素前体在组织中过度产生(进而积累和排泄)的特定模式,是这些疾病各自特征性生化和临床特征的原因。此外,即使存在特定的遗传性酶缺陷,许多不同的环境因素(如药物、热量限制、激素、阳光照射、感染等)通常在引发各种形式卟啉病的临床症状方面起关键作用。由于卟啉病临床表现多样,能够模仿许多其他更常见的疾病,因此常常被误诊。因此,许多不同的专科医生,如外科医生、精神科医生、胃肠病学家、神经科医生、急诊科医生和皮肤科医生,可能会不同程度地参与诊断过程,尤其是对于那些表现出急性和危及生命临床特征的类型。根据临床特征,卟啉病可分为神经精神性(以涉及自主神经系统和中枢神经系统以及肝脏和肾脏的神经内脏危象为特征,可能对神经、心理、心脏、呼吸、肝脏和肾脏功能产生影响)、皮肤病性(主要表现为光敏性引起的皮肤病变)和混合型。从严格的临床角度来看,表现为神经内脏发作的卟啉病也被称为急性卟啉病:它们是本综述的主题。准确诊断急性卟啉病需要了解并使用正确的诊断工具,并且必须提供更合适的治疗方法,防止使用可能严重诱发这些疾病的潜在不安全药物,尤其是在出现危及生命的症状时。迄今为止,一种相对稳定的血红素制剂(精氨酸血红素)的可用性显著改善了急性卟啉病发作的治疗效果,因此关于这些疾病的诊断和管理的知识可能对内科、神经科和急诊科的医生很重要。

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