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血液透析:发展中国家急性间歇性卟啉症严重发作的一种治疗选择。

Hemodialysis: a therapeutic option for severe attacks of acute intermittent porphyria in developing countries.

作者信息

Prabahar Murugesan R, Manorajan Rajendran, Sathiyakumar Devasahayam, Soundararajan Periyasamy, Jayakumar Matcha

机构信息

Department of Nephrology, Sri Ramachandra University, Chennai, India.

出版信息

Hemodial Int. 2008 Jan;12(1):34-8. doi: 10.1111/j.1542-4758.2008.00237.x.

Abstract

Acute intermittent prophyria (AIP) is an autosomal dominant disease that results from a defect in the enzyme porphobilinogen deaminase. Acute intermittent porphyria is the most common of hepatic porphyrias and can tax the therapeutic capabilities of the physician to the limit. Motor weakness is a major feature of an acute attack, and flaccid paralysis of all extremities can occur rapidly, within a matter of days. The acute attacks may be life threatening. Hematin (Heme Arginate) should be given early during an acute attack to prevent neurologic sequel. Hemodialysis and hemoperfusion have been tried in the treatment of acute attacks of AIP with success. As hematin is not available in India, a severe acute attack of AIP in a patient was managed with hemodialysis successfully. Later, hematin was imported and provided to the patient. An 18-year-old girl was admitted to our hospital with recurrent abdominal pain and 2 episodes of convulsions. She had undergone an appendectomy earlier at another hospital for abdominal pain. On evaluation, she had hyponatremia, episodic abnormal behavior, generalized muscle pain, hypertension, and sinus tachycardia. In view of the above clinical picture, a clinical diagnosis of acute intermittent porphyria was made. Her 24-hr urinary porphobilinogen was 90.8 mg/day (<2 mg-normal) and alpha amino levalunic acid was 108.8 mg/day (1-7 mg-normal), consistent with the diagnosis. Her hyponatremia was corrected. Arrangements were made to import hematin and she was managed with dextrose infusion. Meanwhile, she developed flaccid quardriparesis with urinary incontinence and bulbar palsy. Her brain MRI was normal. Her nerve conduction study was suggestive of motor radiculoneuropathy. Specific treatment for severe porphyric crisis was planned. She failed to improve with dextrose infusion alone. As hematin was not readily available in the country, other therapeutic options were considered. As few case reports of AIP being successfully treated with hemodialysis were available, the option of dialytic support was explained to the family. After procuring informed consent, she was subjected to hemodialysis for 4 hr in the first day, increasing to 6 hr a day for the next 6 days. Her abdominal pain and myalgia subsided on the third day of dialysis. Her lower limb muscle power improved and she became ambulant by the fourth day. Urinary retention improved within 4 days. Hematin was imported by then from the United States. Later, 2 doses of hematin (4 mg/kg-160 mg in 20% albumin) were given via a central vein. She was maintained on physiotherapy. Repeat nerve conduction study revealed recovery. She has been provided with a list of drugs that have to be avoided. Currently, she is on outpatient follow-up with occasional abdominal pain, which subsides with intravenous dextrose therapy.

摘要

急性间歇性卟啉病(AIP)是一种常染色体显性疾病,由胆色素原脱氨酶缺陷引起。急性间歇性卟啉病是最常见的肝卟啉病,会极大地考验医生的治疗能力。肌无力是急性发作的主要特征,在几天内所有肢体可能迅速出现弛缓性麻痹。急性发作可能危及生命。在急性发作早期应给予血红素(精氨酸血红素)以预防神经系统后遗症。血液透析和血液灌流已用于治疗AIP急性发作并取得成功。由于印度没有血红素,一名AIP严重急性发作的患者通过血液透析成功得到治疗。后来,进口了血红素并提供给该患者。一名18岁女孩因反复腹痛和2次惊厥发作入院。她早些时候在另一家医院因腹痛接受了阑尾切除术。经评估,她有低钠血症、发作性异常行为、全身肌肉疼痛、高血压和窦性心动过速。鉴于上述临床表现,临床诊断为急性间歇性卟啉病。她24小时尿胆色素原是90.8毫克/天(正常<2毫克),α氨基乙酰丙酸是108.8毫克/天(正常1 - 7毫克),与诊断相符。她的低钠血症得到纠正。安排进口血红素,并用葡萄糖输注对她进行治疗。与此同时,她出现了弛缓性四肢瘫、尿失禁和延髓麻痹。她的脑部磁共振成像正常。她的神经传导研究提示运动性神经根神经病。计划对严重的卟啉病危机进行特异性治疗。仅用葡萄糖输注她未见好转。由于该国不易获得血红素,考虑了其他治疗选择。由于有少数AIP通过血液透析成功治疗的病例报告,向家属解释了透析支持的选择。在获得知情同意后,她第一天接受了4小时血液透析,接下来6天每天增加到6小时。透析第三天她的腹痛和肌痛减轻。第四天她下肢肌肉力量改善并能行走。尿潴留4天内改善。那时已从美国进口了血红素。后来,通过中心静脉给予2剂血红素(4毫克/千克,共160毫克,溶于20%白蛋白)。对她进行物理治疗。重复神经传导研究显示恢复。已给她提供了一份必须避免使用的药物清单。目前,她在门诊随访,偶尔有腹痛,静脉输注葡萄糖治疗后腹痛缓解。

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