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免疫功能低下患者浆母细胞淋巴瘤的碎片化化疗

Fragmented Chemotherapy of Plasmablastic Lymphoma in an Immunocompromised Patient.

作者信息

Chin Sabrina E, Wood Ellen A, Laudat Mandelise N, Santoscoy-Valencia Rodrigo, Fonarov Ilya, Casadesus Damian

机构信息

Internal Medicine, Jackson Memorial Hospital, Miami, USA.

Pathology and Laboratory Medicine, Jackson Memorial Hospital, Miami, USA.

出版信息

Cureus. 2025 Jul 16;17(7):e88102. doi: 10.7759/cureus.88102. eCollection 2025 Jul.

Abstract

Plasmablastic lymphoma (PbL) is an uncommon subtype of diffuse large B-cell lymphoma, which is closely associated with human immunodeficiency virus (HIV) and Epstein-Barr virus(EBV) infections. Due to its rarity and characteristically aggressive nature, it has proven difficult to treat. A rapidly growing mandibular mass can raise suspicion for malignancy. Our patient presented with a painful, enlarging mandibular mass in the absence of fever, night sweats, or fatigue. A review of imaging showed an 8.1 x 5.6 x 9.4 cm central destructive mass with soft tissue swelling, facial skin thickening, and involvement of facial bones. Biopsy was indicative of PbL. The patient was administered a chemotherapy regimen. However, the patient eloped during initial inpatient treatment. The patient returned to the hospital, but subsequent chemotherapy dispensing was irregular and incomplete. Due to the late presentation of the patient and fragmented treatment, the long-term prognosis is poor.

摘要

浆母细胞性淋巴瘤(PbL)是弥漫性大B细胞淋巴瘤的一种罕见亚型,与人类免疫缺陷病毒(HIV)和爱泼斯坦-巴尔病毒(EBV)感染密切相关。由于其罕见性和典型的侵袭性,已证明难以治疗。快速生长的下颌肿块可能会引发对恶性肿瘤的怀疑。我们的患者表现为下颌肿块疼痛且不断增大,无发热、盗汗或疲劳症状。影像学检查显示一个8.1×5.6×9.4厘米的中央破坏性肿块,伴有软组织肿胀、面部皮肤增厚以及面部骨骼受累。活检提示为PbL。该患者接受了化疗方案。然而,患者在初次住院治疗期间逃跑。患者返回医院,但随后的化疗配药不规律且不完整。由于患者就诊较晚且治疗不连贯,长期预后较差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6914/12356603/3769a901a90b/cureus-0017-00000088102-i01.jpg

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