Schmidt´s syndrome found by tan: a case report.

IF 0.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Pan African Medical Journal Pub Date : 2024-06-10 eCollection Date: 2024-01-01 DOI:10.11604/pamj.2024.48.53.35130
Gabriela Venade, Catarina Almeida, Nídia Oliveira, Luis Costa Matos
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引用次数: 0

Abstract

Addison´s disease can form part of type 2 autoimmune polyglandular syndrome. The article reports the case of a 41-year-old female patient with hypothyroidism and vitiligo, who came to the emergency department complaining of asthenia that had worsened in recent months, as well as anorexia, nausea, and weight loss (6 kg in a year). Cutaneous hyperpigmentation was the main finding on physical examination, together with vitiligo lesions on the face, hands, and armpits. Further study revealed a low serum cortisol level, normal urine-free cortisol, and an elevated adrenocorticotropic hormone (ACTH). Antiperoxidase antibodies and 17-alpha-hidroxylase antibodies were both positive. Treatment was started with prednisolone and fludrocortisone, and a good clinical response was obtained. This case report aims to draw attention to the high level of clinical suspicion required to diagnose Addison´s disease and the need to screen actively for other potentially associated autoimmune diseases that may be associated.

通过晒太阳发现的施密特综合征:病例报告。
阿狄森病可能是2型自身免疫性多腺综合征的一部分。文章报告了一例41岁的女性患者,她患有甲状腺功能减退症和白癜风,来急诊科就诊时主诉近几个月来气喘加重、厌食、恶心和体重减轻(一年内体重减轻了6公斤)。体格检查的主要发现是皮肤色素沉着,脸部、手部和腋下也有白癜风皮损。进一步检查发现,患者的血清皮质醇水平较低,尿液中无皮质醇含量正常,促肾上腺皮质激素(ACTH)升高。抗过氧化物酶抗体和17-α-羟化酶抗体均呈阳性。患者开始接受泼尼松龙和氟氢化可的松治疗,并获得了良好的临床反应。本病例报告旨在提请人们注意,诊断阿狄森氏病需要高度临床怀疑,并且需要积极筛查其他可能相关的自身免疫性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pan African Medical Journal
Pan African Medical Journal PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
1.80
自引率
0.00%
发文量
691
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