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失而复得:先天性HIV患者中与艾滋病相关的骨髓抑制被误诊为中性粒细胞减少性发热和良性种族性中性粒细胞减少症

Lost and Found: Misdiagnosis of AIDS-Related Bone Marrow Suppression As Neutropenic Fever and Benign Ethnic Neutropenia in a Patient With Congenital HIV.

作者信息

Huynh Ivy, Woody Dillon M, Ahmed-Khan Mohammad A, Garofalo Victoria, Grisolano Tierney, Willer Quinn

机构信息

Internal Medicine, Danbury Hospital, Danbury, USA.

Behavioral Health, Jackson Memorial Hospital, Miami, USA.

出版信息

Cureus. 2024 Sep 4;16(9):e68632. doi: 10.7759/cureus.68632. eCollection 2024 Sep.

Abstract

Neutropenia is a relatively uncommon but notable secondary effect of HIV infection. While the various hematopoietic effects of HIV and AIDS are well-described in the literature, high-quality evidence directly linking neutropenia with mortality in HIV-infected patients remains limited. The multifactorial etiology of neutropenia complicates its diagnosis, particularly when it occurs secondary to HIV. We present the case of a 35-year-old African American male with congenital HIV, who presented with severe neutropenia accompanied by a fever in the context of untreated HIV. The initial differential diagnosis was broad, including benign ethnic neutropenia (given the patient's African American ethnicity), tuberculosis (given the potential for anti-tuberculosis therapy to cause neutropenia and its commonality as a co-infection in HIV patients), sepsis-related neutropenia, and AIDS-related bone marrow suppression. However, through further workup, it became apparent that HIV-related bone marrow suppression ultimately led to pancytopenia. This case highlights how HIV patient non-adherence to antiretroviral therapy (ART) and hematologic abnormalities complicate the diagnosis of hematopoietic abnormalities from HIV. It also discusses how vertical transmission and abrupt ART discontinuation create a new phenotype of HIV patients with delayed presentations of AIDS-related complications. This patient's presentation also provides insight into the consequences of untreated HIV following the self-discontinuation of long-term HIV management therapy due to low healthcare literacy and loss of follow-up. The patient's clinical course, laboratory findings, imaging studies, and treatment outcomes are discussed, emphasizing the need for timely diagnosis and a multidisciplinary approach to care while exploring potential barriers to care in different social contexts.

摘要

中性粒细胞减少是HIV感染相对不常见但值得注意的继发效应。虽然HIV和艾滋病对造血系统的各种影响在文献中有详细描述,但将中性粒细胞减少与HIV感染患者死亡率直接相关的高质量证据仍然有限。中性粒细胞减少的多因素病因使其诊断复杂化,尤其是当它继发于HIV时。我们报告一例35岁先天性HIV感染的非裔美国男性病例,该患者在未治疗的HIV背景下出现严重中性粒细胞减少并伴有发热。最初的鉴别诊断范围广泛,包括良性种族性中性粒细胞减少(鉴于患者的非裔美国人种族)、结核病(鉴于抗结核治疗可能导致中性粒细胞减少以及其作为HIV患者合并感染的常见性)、脓毒症相关的中性粒细胞减少以及艾滋病相关的骨髓抑制。然而,通过进一步检查,很明显HIV相关的骨髓抑制最终导致了全血细胞减少。该病例突出了HIV患者不坚持抗逆转录病毒治疗(ART)和血液学异常如何使HIV造血异常的诊断复杂化。它还讨论了垂直传播和突然停用ART如何产生一种新的HIV患者表型,其艾滋病相关并发症的表现延迟。该患者的表现还揭示了由于医疗保健知识水平低和失去随访而自行停止长期HIV管理治疗后未治疗HIV的后果。讨论了患者的临床病程、实验室检查结果、影像学研究和治疗结果,强调了及时诊断和多学科护理方法的必要性,同时探讨了不同社会背景下护理的潜在障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b5d/11373367/0ce6c9db2d2e/cureus-0016-00000068632-i01.jpg

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