Transverse myelitis associated with autoimmune polyglandular syndrome type 3B: A case report in Peru

Q4 Medicine
Miguel A. Vences , Milene Morocho-Pinedo , Rossy J. Oliveros-Ramirez , Lizset C. Ballena-Cupe , Julio C. Alvarez-Márquez , Mirla Villafuerte-Espinoza , Diego Urrunaga-Pastor
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引用次数: 0

Abstract

Autoimmune polyglandular syndrome is a rare disease with a low incidence worldwide. We present the case of an adult male with a history of parietal antibody-positive gastritis, central retinal vein obstruction and transverse myelitis. The patient was admitted for exacerbation of myelitis symptoms. The thyroid profile was positive for antibodies, indicating the presence of euthyroid autoimmune thyroid disease. The patient was finally diagnosed with autoimmune polyglandular syndrome type 3B. In the absence of adequate response to methylprednisolone and immunoglobulin, we started treatment with cyclophosphamide and later maintenance therapy with azathioprine. At one year of follow-up, the patient presented paraparesis as sequel, did not present new relapses and control tests were negative for another associated disease.

横断面脊髓炎与自身免疫性多腺综合征3B型:秘鲁1例报告
自身免疫性多腺综合征是一种罕见的疾病,在世界范围内发病率较低。我们提出的情况下,一个成年男性的历史,壁抗体阳性胃炎,中央视网膜静脉阻塞和横断脊髓炎。患者因脊髓炎症状加重而入院。甲状腺抗体呈阳性,提示存在甲状腺功能正常的自身免疫性甲状腺疾病。患者最终被诊断为自身免疫性多腺综合征3B型。由于对甲基强的松龙和免疫球蛋白没有足够的反应,我们开始用环磷酰胺治疗,后来用硫唑嘌呤维持治疗。在一年的随访中,患者表现为继发性麻痹,没有出现新的复发,对照试验为阴性的其他相关疾病。
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来源期刊
Neurologia Argentina
Neurologia Argentina Medicine-Neurology (clinical)
CiteScore
0.50
自引率
0.00%
发文量
34
期刊介绍: Neurología Argentina es la publicación oficial de la Sociedad Neurológica Argentina. Todos los artículos, publicados en español, son sometidos a un proceso de revisión sobre ciego por pares con la finalidad de ofrecer información original, relevante y de alta calidad que abarca todos los aspectos de la Neurología y la Neurociencia.
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