Rivera Rivera Xavier, Baalwa Joshua
Department of Pathology and Laboratory Medicine, The University of Texas Health Sciences Center at Houston, McGovern Medical School, Houston, Texas, USA.
Eur J Case Rep Intern Med. 2021 Jun 11;8(7):002552. doi: 10.12890/2021_002552. eCollection 2021.
Plasmablastic lymphoma (PBL) commonly presents as a primary (de novo) oral or extraoral mucocutaneous or nodal mass lesion in patients with HIV/AIDS. PBL developing as a secondary malignancy at the same location as a pre-existing tumour is extremely rare and has never been reported in association with longstanding or recurrent anal condyloma. A Buschke-Löwenstein tumour is a rare gigantic, locally destructive condyloma that is usually located in the anogenital region. We report a case of a diagnostically and therapeutically challenging PBL that presented as a rapidly enlarging mass underlying a giant condyloma, thereby mimicking a benign Buschke-Löwenstein tumour. Clinical suspicion was further masked by the co-presence of fistulae in ano and adjacent abscess pockets at the time of diagnosis. By the time of final diagnosis, the lymphoma had disseminated to regional lymph nodes, a month later to pleural cavities and 4 months later to the leptomeninges and bilateral kidneys, leading to permanent deferral of chemotherapeutic intervention.
Plasmablastic lymphoma presenting as a secondary tumour in a patient with pre-existing giant anal condyloma has not been reported previously in the literature.Unusual clinical presentation of a recurrent giant condyloma, especially rapid growth and significant change in physical appearance, should kindle a high index of suspicion for a secondary aggressive tumour.Plasmablastic lymphoma disseminates early and rapidly, which complicates its response to treatment.
浆母细胞性淋巴瘤(PBL)在人类免疫缺陷病毒/获得性免疫综合征(HIV/AIDS)患者中通常表现为原发性(新发)口腔或口腔外黏膜皮肤或淋巴结肿块病变。在与先前存在的肿瘤相同部位发展为继发性恶性肿瘤的PBL极为罕见,且从未有与长期或复发性肛门尖锐湿疣相关的报道。Buschke-Löwenstein肿瘤是一种罕见的巨大、局部破坏性尖锐湿疣,通常位于肛门生殖器区域。我们报告一例诊断和治疗具有挑战性的PBL病例,其表现为巨大尖锐湿疣下方迅速增大的肿块,从而酷似良性Buschke-Löwenstein肿瘤。诊断时同时存在肛瘘和相邻脓肿腔进一步掩盖了临床怀疑。最终诊断时,淋巴瘤已扩散至区域淋巴结,1个月后扩散至胸腔,4个月后扩散至软脑膜和双侧肾脏,导致化疗干预永久推迟。
文献中此前未报道过浆母细胞性淋巴瘤在先前存在巨大肛门尖锐湿疣的患者中表现为继发性肿瘤。复发性巨大尖锐湿疣的不寻常临床表现,尤其是快速生长和外观显著变化,应引起对继发性侵袭性肿瘤的高度怀疑。浆母细胞性淋巴瘤早期迅速播散,这使其治疗反应复杂化。