A rare case of diffuse large B-cell lymphoma of the frontal sinus and rapid review of literature.

IF 1.5
Raluca Morar, Norberth Istvan Varga, Ioana Delia Horhat, Ion Cristian Moţ, Flavia Zară, Raluca Maria Cloşca, Cristian Andrei Sarău, Oana Silvana Sarău, Dan Costăchescu, Nicolae Constantin Balica
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Abstract

Introduction: Primary lymphoma of the paranasal sinuses, especially involving the frontal sinus, is exceedingly rare. Extranodal non-Hodgkin lymphoma (NHL) located in the head and neck frequently poses diagnostic challenges because its nonspecific symptoms can be mistaken for benign issues such as rhinosinusitis.

Aim: This case report seeks to emphasize the challenges in diagnosis, the aggressive characteristics, and the effective treatment of an uncommon manifestation of diffuse large B-cell lymphoma (DLBCL) primarily affecting the frontal and ethmoid sinuses.

Case presentation: We present a case of a 62-year-old male who initially presented with symptoms suggestive of acute rhinosinusitis complicated by periorbital cellulitis. Diagnostic workup included physical examination, laboratory investigations, computed tomography (CT) imaging, magnetic resonance imaging (MRI), histopathological (HP) analysis of biopsy specimens, immunohistochemical staining, and positron emission tomography (PET)-CT. The patient presented with right frontal headache, periorbital edema, palpebral ptosis, and posterior rhinorrhea. Initial CT revealed mucosal thickening, lytic changes, and a mass partially invading the right orbit. Following surgical excision, histopathology confirmed DLBCL with positivity for cluster of differentiation (CD)20, CD79a, B-cell lymphoma (Bcl)-6, and Bcl-2, and a Ki-67 proliferation index of 90%. Subsequent MRI revealed a hypointense mass extending into surrounding structures. Staging CT confirmed stage IVB disease. The patient received six cycles of Rituximab-Cyclophosphamide, Hydroxydaunorubicin (Doxorubicin), Oncovin (Vincristine), Prednisolone (R-CHOP) chemotherapy and radiotherapy for the frontal sinus. At the 6-month and 12-month follow-up CT scans, there was no evidence of metabolically active disease on PET-CT (Deauville score 1). During the 2-year follow-up, the patient remained in complete remission.

Conclusions: This case underscores the importance of considering malignancy in cases of atypical sinusitis and the crucial role of HP examination of biopsy specimens. This case also highlights the importance of considering malignancy in cases of atypical sinusitis.

额窦弥漫性大b细胞淋巴瘤一例并快速复习文献。
鼻窦的原发性淋巴瘤,特别是累及额窦,是非常罕见的。结外非霍奇金淋巴瘤(NHL)位于头部和颈部,由于其非特异性症状可能被误认为是良性问题,如鼻窦炎,因此经常给诊断带来挑战。目的:本病例报告旨在强调主要影响额窦和筛窦的弥漫性大b细胞淋巴瘤(DLBCL)的诊断挑战,侵袭性特征和有效治疗。病例介绍:我们提出一个62岁的男性谁最初提出的症状提示急性鼻窦炎合并眼眶周围蜂窝织炎。诊断检查包括体格检查、实验室检查、计算机断层扫描(CT)成像、磁共振成像(MRI)、活检标本的组织病理学(HP)分析、免疫组织化学染色和正电子发射断层扫描(PET)-CT。患者表现为右额部头痛、眶周水肿、眼睑下垂、后鼻漏。初始CT显示粘膜增厚,溶解性改变,肿块部分侵入右眼眶。术后病理证实为DLBCL, CD79a、cd20、Bcl -6、Bcl-2阳性,Ki-67增殖指数90%。随后的MRI显示一个低信号肿块延伸到周围结构。CT确诊为IVB期。患者接受6个周期的利妥昔单抗-环磷酰胺、羟基柔红霉素(多柔红霉素)、Oncovin(长春新碱)、强的松龙(R-CHOP)额窦化疗和放疗。在6个月和12个月的随访CT扫描中,PET-CT未发现代谢活动性疾病的证据(多维尔评分1)。在2年的随访中,患者保持完全缓解。结论:该病例强调了在非典型鼻窦炎病例中考虑恶性肿瘤的重要性以及活检标本HP检查的关键作用。这个病例也强调了在非典型鼻窦炎病例中考虑恶性肿瘤的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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