Pharmacotherapy challenges in HIV patient with Plummer-Vinson Syndrome

Priya Manirajan, Palanisamy Sivanandy
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引用次数: 0

Abstract

Plummer-Vinson Syndrome (PVS) is a rare condition characterized by the classic triad of dysphagia, iron-deficiency anemia or long-standing anemia, and esophageal web. We present a case of a 38-year-old man who was diagnosed with human immunodeficiency virus, underwent antiretroviral therapy, and faced challenges starting Highly Active Antiretroviral Therapy (HAART) medications due to their size. An esophagogastroduodenoscopy revealed that the patient has Plummer-Vinson Syndrome. Healthcare providers encountered difficulties in optimizing his therapy and initiating HAART medication for his HIV treatment. We present this case due to its rarity.
普卢默-文森综合征HIV患者的药物治疗挑战
普卢默-文森综合征(PVS)是一种罕见的疾病,其特征是吞咽困难、缺铁性贫血或长期贫血和食管网。我们报告了一个38岁的男性病例,他被诊断患有人类免疫缺陷病毒,接受了抗逆转录病毒治疗,并且由于药物的大小而面临开始高活性抗逆转录病毒治疗(HAART)的挑战。食管胃十二指肠镜检查显示患者患有普卢默-文森综合征。医疗保健提供者在优化他的治疗和为他的艾滋病毒治疗启动HAART药物方面遇到了困难。我们提出这个案例是因为它的罕见性。
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