Colna Antonio N´fad, Togo Mamadu, Pr. Yassine Er-Rahali, Pr. Ahmed Anass Guerboub
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Clinically the patient was asthenic, she had arthralgia and myalgia with anorexia contrasting an appetite for salt with notion of fasting hypoglycemia without melanoderma or vitiligo, the rest of the clinical examination was unremarkable. Weight: 65 kg; Height: 1.69 m; BMI: 23Kg/m²; TT: 70 cm; Pulse: 64 bpm. BP: 110/60 mm Hg in the right arm standing and lying down. Biological exploration found low 08 h plasma cortisol with high ACTH, high TSH and anti-TPO antibodies, and macrocytic normochromic anemia at 8 g/dl with anti-parietal cell antibodies and intrinsic factor have positive. whose explorations were in favor of Biermer's disease. The diagnosis of PEA type 2 was made. The treatment recommended: hormonal replacement of adrenal and thyroid insufficiency as well as vitamin B12 injections with good clinical and biological progress.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Autoimmune Polyendocrinopathy Type 2 (PEA Type) Associated with Biermer's Disease: Report of a Case and Review of the Literature\",\"authors\":\"Colna Antonio N´fad, Togo Mamadu, Pr. Yassine Er-Rahali, Pr. Ahmed Anass Guerboub\",\"doi\":\"10.36347/sjmcr.2024.v12i04.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Autoimmune polyendocrinopathy type II (AIEP II) is a more common syndrome that appears mainly in adults. It combines several autoimmune pathologies including Addison's disease and autoimmune thyroid disease (Schmidt syndrome) and/or type 1 diabetes (Carpenter syndrome). We report the case of a 16-year-old patient with notable familial pathological ATCD: Father followed by high blood pressure under antihypertensive treatment and type 2 diabetes under oral anti-diabetes medication. Mother followed for hypothyroidism under hormone replacement treatment with levothyroxine. The patient was followed for hypothyroidism for 2 years, hospitalized in our training for suspicion of adrenal insufficiency. Clinically the patient was asthenic, she had arthralgia and myalgia with anorexia contrasting an appetite for salt with notion of fasting hypoglycemia without melanoderma or vitiligo, the rest of the clinical examination was unremarkable. Weight: 65 kg; Height: 1.69 m; BMI: 23Kg/m²; TT: 70 cm; Pulse: 64 bpm. BP: 110/60 mm Hg in the right arm standing and lying down. Biological exploration found low 08 h plasma cortisol with high ACTH, high TSH and anti-TPO antibodies, and macrocytic normochromic anemia at 8 g/dl with anti-parietal cell antibodies and intrinsic factor have positive. whose explorations were in favor of Biermer's disease. The diagnosis of PEA type 2 was made. 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引用次数: 0
摘要
自身免疫性多内分泌病 II 型(AIEP II)是一种更常见的综合征,主要出现在成年人身上。它结合了多种自身免疫性病变,包括阿狄森氏病和自身免疫性甲状腺疾病(施密特综合征)和/或 1 型糖尿病(卡彭特综合征)。我们报告了一例 16 岁患者的病例,该患者具有明显的家族病理 ATCD:父亲因高血压接受降压治疗,2 型糖尿病接受口服抗糖尿病药物治疗。母亲因甲状腺功能减退接受左甲状腺素激素替代治疗。患者因甲状腺功能减退症接受了两年的随访,因怀疑肾上腺功能不全而在我院住院治疗。临床上,该患者体质虚弱,有关节痛和肌痛,伴有厌食,食盐量少,有空腹低血糖症状,无黑色素瘤或白癜风,其他临床检查无异常。体重:65 千克;身高:1.69 米;体重指数:23 千克/平方米;TT:70 厘米;脉搏:64 次/分。血压:右臂站立和平卧时均为 110/60 mm Hg。生物学检查发现 08 h 血浆皮质醇偏低,ACTH 偏高,促甲状腺激素(TSH)和抗-TPO 抗体偏高,大红细胞正常色素性贫血(8 g/dl),抗顶叶细胞抗体和内在因子呈阳性。诊断结果为 PEA 2 型。治疗建议:肾上腺和甲状腺功能不全的激素替代以及维生素 B12 注射,临床和生物学进展良好。
Autoimmune Polyendocrinopathy Type 2 (PEA Type) Associated with Biermer's Disease: Report of a Case and Review of the Literature
Autoimmune polyendocrinopathy type II (AIEP II) is a more common syndrome that appears mainly in adults. It combines several autoimmune pathologies including Addison's disease and autoimmune thyroid disease (Schmidt syndrome) and/or type 1 diabetes (Carpenter syndrome). We report the case of a 16-year-old patient with notable familial pathological ATCD: Father followed by high blood pressure under antihypertensive treatment and type 2 diabetes under oral anti-diabetes medication. Mother followed for hypothyroidism under hormone replacement treatment with levothyroxine. The patient was followed for hypothyroidism for 2 years, hospitalized in our training for suspicion of adrenal insufficiency. Clinically the patient was asthenic, she had arthralgia and myalgia with anorexia contrasting an appetite for salt with notion of fasting hypoglycemia without melanoderma or vitiligo, the rest of the clinical examination was unremarkable. Weight: 65 kg; Height: 1.69 m; BMI: 23Kg/m²; TT: 70 cm; Pulse: 64 bpm. BP: 110/60 mm Hg in the right arm standing and lying down. Biological exploration found low 08 h plasma cortisol with high ACTH, high TSH and anti-TPO antibodies, and macrocytic normochromic anemia at 8 g/dl with anti-parietal cell antibodies and intrinsic factor have positive. whose explorations were in favor of Biermer's disease. The diagnosis of PEA type 2 was made. The treatment recommended: hormonal replacement of adrenal and thyroid insufficiency as well as vitamin B12 injections with good clinical and biological progress.