首页> 外文期刊>American Journal of Dermatology and Venereology >Generalized Hyperpigmentation, in Sudanese Patient with Primary Addison’s Disease as Autoimmune Manifestation of Extra Digestive Helicobacter pylori Infection
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Generalized Hyperpigmentation, in Sudanese Patient with Primary Addison’s Disease as Autoimmune Manifestation of Extra Digestive Helicobacter pylori Infection

机译:苏丹原发性阿迪森氏病为过度消化性幽门螺杆菌感染的自身免疫性表现的全身性色素沉着过度

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Addison's disease, or chronic adrenocortical insufficiency, is the overproduction of adrenocorticotropic hormone, ACTH, by the pituitary gland as a compensatory mechanism for decreased cortisol production by the adrenal glands. Classically, patients affected with Addison's disease develop weakness, anorexia, electrolyte imbalances: decreased sodium and chloride with increased serum potassium resulting in hypotension, and hyperpigmentation of the skin and mucous membranes.We report an undiagnosed localized hyperpigmented primary autoimmune Addison’s disease as extra digestive manifestation of Helicobacter pylori infection in a 43 years old male patient, teacher, who presented with localized Palmar dark pigmentation, for 7 months duration. The case was diagnosed and confirmed by ACTH stimulating test and cortisol blood level, and is considered to be the first case (reported in Sudan) associated with H. pylori and it responded to triple therapy.
机译:艾迪生氏病(或慢性肾上腺皮质功能不全)是垂体促肾上腺皮质激素过剩,ACTH作为肾上腺皮质醇生成减少的补偿机制。通常,患有Addison病的患者会出现虚弱,厌食,电解质失衡:钠和氯化物减少,血清钾增加,导致低血压以及皮肤和粘膜色素沉着过度。我们报告未诊断为局部色素沉着的原发性自身免疫性Addison病为额外的消化系统表现。一名43岁男性患者,老师的幽门螺杆菌感染的报告,该患者出现了局部的Palmar黑色色素沉着,持续了7个月。该病例通过促肾上腺皮质激素刺激试验和皮质醇血药水平诊断并确诊,被认为是与H相关的第一例(苏丹报告)。幽门螺杆菌,它对三联疗法有反应。

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