Bothra Nandini, Ali Mohammad J
Govindram Seksaria Institute of Dacryology, L.V Prasad Eye Institute, Hyderabad, Telengana, India.
Saudi J Ophthalmol. 2025 May 23;39(2):185-187. doi: 10.4103/sjopt.sjopt_66_25. eCollection 2025 Apr-Jun.
Mantle cell lymphoma (MCL) of the lacrimal sac is an exceptionally rare tumor with only four such cases reported in literature, to the best of authors' knowledge. The tumor is known to have extensive systemic and bone marrow involvement with poor prognosis and overall survival. The present case describes a 64-year-old male with primary MCL of the lacrimal drainage system, its diagnosis, and treatment options.
泪囊套细胞淋巴瘤(MCL)是一种极其罕见的肿瘤,据作者所知,文献中仅报道过4例此类病例。已知该肿瘤会广泛累及全身及骨髓,预后和总生存率较差。本病例描述了一名64岁男性,患有泪道系统原发性MCL,以及其诊断和治疗方案。