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Psoriasis and Glucose-6 Phosphate Dehydrogenase Deficiency: A Rare Association?

机译:牛皮癣和葡萄糖6磷酸脱氢酶缺乏症:罕见的协会?

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Glucose-6 phosphate dehydrogenase (G6PD) is a vital enzyme for erythrocytes to be protected against oxidative stress. Its deficiency is the most common erythrocyte enzyme defect. Deficiency can cause acute or chronic hemolysis episodes. Hemolysis can be augmented by infections or drug use. Psoriasis is a complex autoimmune disorder characterized by skin involvement with inflammatory plaques. An otherwise healthy 37 years old male patient presented to internal medicine outpatient clinic with fatigue, generalized pain and skin lesions. Patient states that his sypmtoms got worse and worse after he took those medications. His past medical history was unremarkable. His family history reveals that his brother’s son was recently diagnosed with G6PD deficiency. Quantitavite G6PD enzyme assay did not reveal any enzyme activity. Results were consistent with chronic hemolysis and G6PD enzyme deficiency was diagnosed as the cause. Patient’s skin lesions were consulted with dermatology and he was diagnosed with psoriasis. Because he had G6PD deficiency, he was only prescribed topical treatment. The patient was relieved of all generalized body pain. Here we present a case who presented with erythematous and squamataous plaques and malaise/generalized pain, diagnosed with G6PD deficiency and psoriasis. We discuss the possible relationship between two conditions.J Med Cases. 2015;6(11):493-497doi: http://dx.doi.org/10.14740/jmc2318e
机译:6磷酸葡萄糖脱氢酶(G6PD)是保护红细胞免受氧化应激的重要酶。它的缺乏是最常见的红细胞酶缺陷。缺乏会导致急性或慢性溶血。感染或吸毒会加剧溶血。牛皮癣是一种复杂的自身免疫性疾病,其特征在于皮肤受累于炎症斑块。另一名健康的37岁男性患者因疲劳,广泛性疼痛和皮肤病变而就诊于内科门诊。患者指出,服用这些药物后他的症状越来越严重。他过去的病史并不明显。他的家族史显示,他兄弟的儿子最近被诊断出患有G6PD缺乏症。 Quantitavite G6PD酶分析未发现任何酶活性。结果与慢性溶血相符,诊断为G6PD酶缺乏症。患者的皮肤病变经过皮肤科咨询,他被诊断出患有牛皮癣。由于他患有G6PD缺乏症,因此仅接受局部治疗。病人所有的全身疼痛得到缓解。在这里,我们介绍一个病例,该病例表现出红斑和鳞状斑块和不适/全身性疼痛,被诊断出患有G6PD缺乏症和牛皮癣。我们讨论了两个条件之间的可能关系。 2015; 6(11):493-497doi:http://dx.doi.org/10.14740/jmc2318e

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