一个罕见的慢性炎症性脱髓鞘多发性神经病(cidp)和急性横贯性脊髓炎(atm)混合病例。

Q4 Medicine
West African journal of medicine Pub Date : 2024-11-10
K Thomas, M Danso, G Goddard, H D Maydoilis, S M Oguche, T Bello, C H Njoku, O R Obiako
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引用次数: 0

摘要

简介/背景:虽然 CIDP 和 ATM 都是神经系统炎症性疾病,但它们很少同时出现在同一个人身上:一名 41 岁的男性交易者因截瘫和上肢无力 10 天病史入院。起病时下肢麻痹,左腿无力,5 天后右腿无力,3 天后出现截瘫、上臂无力、尿潴留和便秘。他曾短暂发烧,没有咽喉痛或咳嗽,没有出国旅行,也没有接种疫苗。他每年吸烟 10 包,偶尔饮酒。他未婚。生命体征稳定,精神正常;血氧饱和度 98%;无颅神经功能缺损;弛缓性截瘫;双上肢弛缓性无力(MRC 1/5),对称性感觉减退至 T4 水平。艾滋病毒、乙型肝炎和丙型肝炎抗体均为阴性;血液学、肾脏和肝功能正常。核磁共振成像显示,CSF 细胞白蛋白分离以及颈椎和上胸椎脊髓高密度,因此有必要诊断为混合型 CIDP 和 ATM。虽然患者无法购买静脉注射免疫球蛋白,但他一直在服用泼尼松龙;40 天后,弛缓性截瘫和感觉缺失仍然存在,但张力和反射已恢复正常,力量为 MRC 3/5。他仍有意识,呼吸困难,目前使用机械呼吸机,鼻胃管和导尿管仍在进食:结论:CIDP 和 ATM 都是不同的严重神经炎症性疾病,需要急诊和重症监护治疗,因为这两种疾病都有可能导致高死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A RARE CASE OF MIXED CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULOPATHY (CIDP) AND ACUTE TRANSVERSE MYELITIS (ATM).

Introduction/background: Though CIDP and ATM are both inflammatory disorders of the nervous system with distinct features, they rarely occur together in the same individual.

Case presentation: A 41-year-old male trader was admitted with 10 10-day history of paraplegia and weakness of upper limbs. The illness started with lower limb paresthesia, weakness of the left leg, then the right leg after 5 days, proceeding to paraplegia, weakness of upper arms, urine retention, and constipation 3 days before presentation. There was a brief fever; no sore throat or cough; no travel outside the country; and no vaccination. He smoked 10 cigarette packs yearly and drank alcohol occasionally. He was unmarried. Vital signs were stable with normal mentation; oxygen saturation 98%; no cranial nerve deficits; flaccid paraplegia; flaccid bilateral upper limbs weakness (MRC 1/5) and symmetrical sensory loss to the level of T4. HIV, hepatitis B, and C antibodies were all negative; hematological, renal, and liver functions were normal. CSF cyto-albumin dissociation and hyperintensities of the cervical and upper thoracic spinal cord on MRI necessitated a diagnosis of mixed CIDP and ATM. Although the patient could not buy IV immunoglobulin, he has been on prednisolone; and 40 days later flaccid paraplegia and sensory loss persist, but tone and reflexes have returned to normal, and power is MRC 3/5. He remains conscious, is dyspnoeic, and is currently on a mechanical ventilator with a feeding nasogastric tube and urinary catheter in situ.

Conclusion: Both CIDP and ATM are distinct severe neuro-inflammatory diseases requiring emergency and intensive care management as each has potential for high mortality outcomes.

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来源期刊
West African journal of medicine
West African journal of medicine Medicine-Medicine (all)
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