Narváez-García Erwin J, Pacheco-Carrillo Aldo M, Ortiz-Villeda Flor E, Salinas-Chapa Matías, Elizondo-Riojas Guillermo, Franco-Marquez Rodolfo
Radiology, Hospital Universitario "Dr. José Eleuterio González", Monterrey, MEX.
Pathology, Hospital Universitario "Dr. José Eleuterio González", Monterrey, MEX.
Cureus. 2025 Aug 22;17(8):e90741. doi: 10.7759/cureus.90741. eCollection 2025 Aug.
Plasmablastic lymphoma (PBL) is an uncommon and aggressive subtype of diffuse large B-cell lymphoma (DLBCL), strongly linked to immunosuppressed states. Although it most frequently involves the oral cavity, anorectal presentation is exceptionally rare. We describe the case of a 27-year-old male with a recent human immunodeficiency virus (HIV) diagnosis, who presented with a growing perianal mass and rectal bleeding. The lesion progressed despite initial treatment and required surgical management. Imaging revealed a necrotic anal canal mass with soft tissue invasion, and histopathology confirmed the diagnosis of PBL. The patient underwent chemotherapy but ultimately experienced a poor clinical outcome. Due to its rarity and non-specific presentation, anorectal PBL is often misdiagnosed, delaying definitive treatment. Imaging, particularly magnetic resonance imaging (MRI), is essential for evaluating lesion extent and guiding clinical decisions. Despite available therapies, the prognosis remains guarded. This case highlights the importance of considering PBL in the differential diagnosis of atypical anorectal masses in immunosuppressed patients. Early imaging and histopathologic assessment are vital for timely diagnosis and treatment.
浆母细胞性淋巴瘤(PBL)是弥漫性大B细胞淋巴瘤(DLBCL)的一种罕见且侵袭性的亚型,与免疫抑制状态密切相关。尽管它最常累及口腔,但肛门直肠表现极为罕见。我们描述了一名27岁男性病例,该患者最近被诊断为人类免疫缺陷病毒(HIV)感染,出现肛周肿物增大及直肠出血症状。尽管最初进行了治疗,但病变仍进展,需要手术处理。影像学检查显示肛管有坏死性肿物并侵犯软组织,组织病理学确诊为PBL。患者接受了化疗,但最终临床结局不佳。由于其罕见性及非特异性表现,肛门直肠PBL常被误诊,从而延误确定性治疗。影像学检查,尤其是磁共振成像(MRI),对于评估病变范围及指导临床决策至关重要。尽管有可用的治疗方法,但其预后仍不容乐观。该病例强调了在免疫抑制患者非典型肛门直肠肿物的鉴别诊断中考虑PBL的重要性。早期影像学和组织病理学评估对于及时诊断和治疗至关重要。