Davuluri Srikanth, Jandali Majed, Paul Tyler, Wind Kenneth
Pulmonary and Critical Care Medicine, Rosalind Franklin University of Medicine and Sciences, North Chicago, USA.
Pulmonary and Critical Care Medicine, Froedtert South Pleasant Prairie Hospital, Pleasant Prairie, USA.
Cureus. 2025 Sep 8;17(9):e91859. doi: 10.7759/cureus.91859. eCollection 2025 Sep.
Post-transplant lymphoproliferative disorder (PTLD) is a rare but fatal outcome following solid organ transplant, which is often associated with Epstein-Barr virus (EBV) infection or immunosuppression. Subsequent gastrointestinal involvement is uncommon and can lead to severe complications. We describe a 58-year-old male who developed EBV-associated PTLD within six months of a deceased donor renal transplant who presented with persistent severe gastrointestinal bleeding. Multiple surgical resections were required as the patient also developed progressive ischemic bowel disease. Despite immunosuppression reduction, rituximab therapy, and surgical intervention, his condition worsened and led to multi-organ failure and eventually death. This case highlights the aggressive clinical course of gastrointestinal-associated PTLD and the challenges in diagnosis and management. Early recognition with multidisciplinary care is critical for treatment, but may be insufficient in cases with advanced disease. EBV monitoring and tailored immunosuppression in transplant recipients are also essential in improving outcomes in high-risk patients.
移植后淋巴细胞增生性疾病(PTLD)是实体器官移植后一种罕见但致命的后果,通常与爱泼斯坦-巴尔病毒(EBV)感染或免疫抑制有关。随后累及胃肠道的情况并不常见,但可导致严重并发症。我们描述了一名58岁男性,在接受已故供体肾移植后6个月内发生了与EBV相关的PTLD,表现为持续性严重胃肠道出血。由于患者还出现了进行性缺血性肠病,需要进行多次手术切除。尽管减少了免疫抑制、进行了利妥昔单抗治疗和手术干预,但其病情仍恶化,导致多器官功能衰竭并最终死亡。该病例突出了胃肠道相关PTLD的侵袭性临床病程以及诊断和管理方面的挑战。早期通过多学科护理进行识别对治疗至关重要,但在疾病晚期的病例中可能并不足够。对移植受者进行EBV监测和定制免疫抑制对于改善高危患者的预后也至关重要。