Gandhi Tanmay, Shah Aniruddh, Thakurdesai Aishwarya
Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, USA.
Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, USA.
Cureus. 2022 Dec 30;14(12):e33151. doi: 10.7759/cureus.33151. eCollection 2022 Dec.
Plasmablastic lymphoma (PbL) is a rare type of aggressive B-cell malignancy that has an extremely poor prognosis without chemotherapeutic treatment, requiring a high degree of suspicion for an early and accurate diagnosis. It has been classically described in patients infected with the human immunodeficiency virus (HIV). However, it accounts for only 2.6% of acquired immunodeficiency syndrome (AIDS)-related lymphomas. Extranodal involvement is most commonly seen within the oral cavity (44%). Involvement of the gastrointestinal tract (14%) is rare and can often be confused with other malignancies with plasmablastic features. We present a rare case of PbL in a 55-year-old male with HIV-AIDS (CD4 (cluster of differentiation 4) cell count of 128), who presented for evaluation of incidentally detected multiple liver masses and lytic lesions in the ribs. Further workup revealed evidence of a lesion with increased uptake in the anorectal region with fine needle aspiration (FNA) biopsy identifying the lesion as plasmablastic lymphoma.
浆母细胞淋巴瘤(PbL)是一种罕见的侵袭性B细胞恶性肿瘤,若不进行化疗,预后极差,因此早期准确诊断需要高度怀疑。经典报道显示其多见于感染人类免疫缺陷病毒(HIV)的患者。然而,它仅占获得性免疫缺陷综合征(AIDS)相关淋巴瘤的2.6%。结外受累最常见于口腔(44%)。胃肠道受累(14%)较为罕见,常易与具有浆母细胞特征的其他恶性肿瘤混淆。我们报告一例罕见的55岁男性HIV-AIDS患者(CD4(分化簇4)细胞计数为128)的PbL病例,该患者因偶然发现的多个肝脏肿块和肋骨溶骨性病变前来评估。进一步检查发现,经细针穿刺抽吸(FNA)活检,在肛门直肠区域发现一个摄取增加的病变,病理结果确诊为浆母细胞淋巴瘤。