Hematophagocytic Syndrome in a Patient Co-Infected With HIV: A Case Report

Romero-Sánchez Alan Jesús, Pérez Licona Cristal Dánae, Velázquez Orozco Paola, Pérez García José Antonio
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Abstract

Introduction: Hemophagocytic syndrome is a severe disease characterized by a state of systemic hyperinflammation with overproduction of cytokines. It can respond to genetic causes (primary) or be triggered by infections, drugs, neoplasms or autoimmune diseases. With increased mortality. We present the case of a patient with HIV who developed hemophagocytic syndrome during hospitalization. Case presentation: We present the case of a male patient with human immunodeficiency virus who developed hemophagocytic syndrome with lymphadenopathies and biopsy report concluding the syndromic suspicion. Conclusions: Our case report reflects the clinical and biochemical approach to hemophagocytic syndrome, in which the realization of a histopathological diagnosis was determinant to reflect the cause of the disease in question, we denote the importance of clinical suspicion in infrequent situations related to the patient with immunodeficiency.
一名合并感染艾滋病毒患者的嗜血细胞综合征:病例报告
导言嗜血细胞综合征是一种严重的疾病,其特征是全身性高炎症状态和细胞因子的过度分泌。它可以由遗传原因(原发性)引起,也可以由感染、药物、肿瘤或自身免疫性疾病诱发。这种疾病会增加死亡率。我们介绍了一例在住院期间患上嗜血细胞综合征的艾滋病患者。病例介绍:我们介绍了一名男性人类免疫缺陷病毒感染者的病例,他患上了嗜血细胞综合征并伴有淋巴结病,活检报告得出了综合征怀疑结论。结论:我们的病例报告反映了嗜血细胞综合征的临床和生化方法,其中组织病理学诊断的实现是反映相关疾病病因的决定性因素。
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