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一名人类免疫缺陷病毒阳性患者出现乙状结肠直肠穿孔的浆母细胞淋巴瘤

Plasmablastic Lymphoma Presenting With Rectosigmoid Perforation in a Human Immunodeficiency Virus-Positive Patient.

作者信息

Zafar Muhammad H, Gil Lola C, Karimi Saman, Arain Saad, Niravel Bindu, Martinolich Jessica, Galvin John, Murga-Zamolloa Carlos A, Gantt Gerald

机构信息

Department of Colorectal Surgery, University of Illinois at Chicago, Chicago, USA.

Department of Pathology, University of Illinois at Chicago, Chicago, USA.

出版信息

Cureus. 2022 May 13;14(5):e24964. doi: 10.7759/cureus.24964. eCollection 2022 May.

DOI:10.7759/cureus.24964
PMID:35706759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9187260/
Abstract

Plasmablastic lymphoma (PBL) is a rare variant of diffuse large B-cell lymphoma (DLBCL) associated with human immunodeficiency virus (HIV)-positive patients. It accounts for only 2% of all acquired immune deficiency syndrome (AIDS)-related lymphomas (ARLs). We present the case of a 45-year-old male who presented to the emergency department (ED) with a three-month history of abdominal pain, diarrhea, and unintentional 50-lb weight loss. On an earlier presentation to the ED three months prior, the patient was diagnosed with norovirus and infection and received outpatient treatment without resolution of his symptoms. This prompted further investigation with a CT of the abdomen and pelvis with IV contrast that revealed severe sigmoid colitis with pneumoperitoneum and a pericolonic air-containing fluid collection, consistent with a contained perforation with abscess formation. He was admitted, resuscitated, and initially treated with antibiotics and parenteral nutrition. The patient underwent a laparoscopic converted to open anterior resection with end colostomy. Pathology revealed HIV-related PBL. He was subsequently treated with dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (DA-EPOCH-R) chemotherapy regimen and an autologous stem cell transplant. Despite its rare association with HIV, PBL should be considered a differential diagnosis for HIV-positive patients who present with gastrointestinal (GI) pathology, and additional investigations should be conducted if symptoms do not resolve despite appropriate medical management at the time.

摘要

浆母细胞淋巴瘤(PBL)是弥漫性大B细胞淋巴瘤(DLBCL)的一种罕见变异型,与人类免疫缺陷病毒(HIV)阳性患者相关。它仅占所有获得性免疫缺陷综合征(AIDS)相关淋巴瘤(ARL)的2%。我们报告一例45岁男性病例,该患者因腹痛、腹泻和意外减重50磅,有3个月病史,前来急诊科就诊。3个月前该患者曾较早前来急诊科就诊,当时被诊断为诺如病毒感染,接受了门诊治疗,但症状未缓解。这促使进一步行腹部和盆腔CT增强扫描,结果显示严重乙状结肠炎伴气腹和结肠周围含气液性包块,符合局限性穿孔伴脓肿形成。患者入院后接受复苏治疗,最初给予抗生素和肠外营养治疗。患者接受了腹腔镜转为开放的前切除术并做了结肠造口术。病理检查显示为HIV相关的PBL。随后他接受了剂量调整的依托泊苷、泼尼松、长春新碱、环磷酰胺、多柔比星和利妥昔单抗(DA-EPOCH-R)化疗方案以及自体干细胞移植。尽管PBL与HIV的关联罕见,但对于出现胃肠道(GI)病变的HIV阳性患者,应考虑将PBL作为鉴别诊断之一,如果在当时进行了适当的药物治疗后症状仍未缓解,则应进行进一步检查。

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