Avalos Gonzalez Guillermo, Gasga Velasco Mariana Carolina, Rosales Verduzco Paola V, Rodríguez Hernández Ana Laura, Enríquez Plascencia Pablo Yael, Gutierrez Plascencia Dina Paola, Garcia Santiago Gerardo
Internal Medicine, Hospital Regional Dr. Valentín Gómez Farías - Institute for Social Security and Services for State Workers or Civil Service Social Security and Services Institute (ISSSTE), Zapopan, MEX.
General Medicine, Universidad Autónoma de Guadalajara, Guadalajara, MEX.
Cureus. 2025 Aug 25;17(8):e90991. doi: 10.7759/cureus.90991. eCollection 2025 Aug.
HIV-associated cholangiopathy (HAC) is a rare but clinically important hepatobiliary complication occurring in patients with advanced immunosuppression, particularly those with cluster of differentiation 4+ (CD4+) counts below 100 cells/μL. It is most often triggered by opportunistic infections and can present as a spectrum of biliary abnormalities that result in cholestasis and obstruction. We present the case of a 58-year-old man with a history of HIV infection (B24) under regular follow-up, with an undetectable CD4 count and elevated viral load, who presented to the emergency department with jaundice, severe right upper quadrant and epigastric abdominal pain, nausea, vomiting, and a 10 kg weight loss over the past month. During hospitalization, a complex distal common bile duct (CBD) stricture was identified, accompanied by acute cholangitis, obstructive pancreatitis, and acute kidney injury (AKI) on a background of chronic kidney disease (CKD). The patient underwent endoscopic retrograde cholangiopancreatography (ERCP) with biliary stent placement, resulting in clinical improvement. HIV-associated cholangiopathy was confirmed as the underlying diagnosis. This case highlights the need to consider HAC in immunosuppressed patients presenting with cholestatic liver profiles and supports the importance of timely endoscopic intervention and multidisciplinary management.
人类免疫缺陷病毒相关性胆管病(HAC)是一种罕见但临床上重要的肝胆并发症,发生于晚期免疫抑制患者,尤其是那些分化簇4 +(CD4 +)计数低于100个细胞/μL的患者。它最常由机会性感染引发,可表现为一系列导致胆汁淤积和梗阻的胆道异常。我们报告一例58岁男性病例,该患者有人类免疫缺陷病毒感染史(B24),正在接受定期随访,CD4计数检测不到且病毒载量升高,因黄疸、严重右上腹和上腹部疼痛、恶心、呕吐以及过去一个月体重减轻10千克就诊于急诊科。住院期间,发现一个复杂的胆总管远端狭窄,并伴有急性胆管炎、梗阻性胰腺炎以及慢性肾脏病(CKD)背景下的急性肾损伤(AKI)。患者接受了内镜逆行胰胆管造影术(ERCP)并置入胆道支架,临床症状改善。确诊潜在诊断为人类免疫缺陷病毒相关性胆管病。该病例强调了在出现胆汁淤积性肝病表现的免疫抑制患者中需要考虑HAC,并支持及时进行内镜干预和多学科管理的重要性。