Agarwal Ashish Chandra, Hussain Nuzhat, Kumar Vineet
Department of ENT, Dr. Ram Manohar Lohia Institute of Medical sciences, Lucknow, Uttar Pradesh India.
Department of Pathology, Dr. Ram Manohar Lohia Institute of Medical sciences, Lucknow, Uttar Pradesh India.
Indian J Otolaryngol Head Neck Surg. 2025 Jun;77(6):2438-2441. doi: 10.1007/s12070-025-05505-5. Epub 2025 May 2.
Diffuse Large B-Cell Lymphoma (DLBCL) of the paranasal sinuses (PNS) is an uncommon manifestation of non-Hodgkin lymphoma (NHL), accounting for 0.2-2% of all DLBCL cases. Despite DLBCL being the most frequent subtype of NHL, its occurrence in the PNS is rare, often leading to diagnostic delays due to nonspecific symptoms. The disease primarily affects older adults with a slight male predominance and presents with nasal obstruction, proptosis, and vision loss, among other symptoms. Diagnosis is challenging due to its similarity to more common sinonasal conditions like sinusitis, and timely identification is crucial given DLBCL's aggressive nature. This report presents three cases of DLBCL in the PNS, each characterized by progressive symptoms such as headache, nasal discharge, proptosis, and vision loss. All three patients were treated in a tertiary care center in North India. In each case, diagnostic imaging, histopathological examination, and immunohistochemical staining were utilized to confirm DLBCL. The patients underwent endoscopic biopsy and received chemotherapy, with varying degrees of response. Treatment challenges, particularly in patients with advanced disease, were highlighted, including the potentialfor irreversible vision loss and the high risk of relapse. A literature review further supports that DLBCL of the PNS is a rare but significant diagnosis requiring prompt recognition and treatment. Review of similar cases emphasizes the importance of distinguishing this condition from other sinonasal tumorsand infections to ensure proper management and improved patient outcomes.
鼻窦弥漫性大B细胞淋巴瘤(DLBCL)是非霍奇金淋巴瘤(NHL)的一种罕见表现形式,占所有DLBCL病例的0.2 - 2%。尽管DLBCL是NHL最常见的亚型,但其在鼻窦的发生却很罕见,常因症状不具特异性而导致诊断延迟。该疾病主要影响老年人,男性略占优势,表现为鼻塞、眼球突出和视力丧失等症状。由于其与鼻窦炎等更常见的鼻窦疾病相似,诊断具有挑战性,鉴于DLBCL的侵袭性,及时识别至关重要。本报告介绍了3例鼻窦DLBCL病例,每例均以头痛、流涕、眼球突出和视力丧失等进行性症状为特征。所有3例患者均在印度北部的一家三级医疗中心接受治疗。在每例病例中,均利用诊断性影像学检查、组织病理学检查和免疫组化染色来确诊DLBCL。患者接受了内镜活检并接受化疗,反应程度各异。强调了治疗挑战,尤其是在晚期疾病患者中,包括不可逆视力丧失的可能性和高复发风险。文献综述进一步支持鼻窦DLBCL是一种罕见但重要的诊断,需要及时识别和治疗。对类似病例的回顾强调了将这种疾病与其他鼻窦肿瘤和感染区分开来以确保正确管理和改善患者预后的重要性。