Alghamdi Abdulmalik H, Alzahrani Mazen, Kamal Yumna F, Aljehani Reham, Ibrahim Islam A, Alqahtani Abdullah S
Ophthalmology, College of Medicine, Taif University, Taif, SAU.
Ophthalmology, Jeddah Eye Hospital, Jeddah, SAU.
Cureus. 2024 Jul 3;16(7):e63725. doi: 10.7759/cureus.63725. eCollection 2024 Jul.
Burkitt lymphoma is an aggressive B-cell non-Hodgkin lymphoma (NHL). Primary CNS lymphoma (PCNSL) is a rare disease, and the subtype of Burkitt lymphoma presenting as a sole CNS lesion is an even rarer diagnosis. Acute sudden blindness is a rare presenting symptom of PCNSL or NHL in general. We present an interesting case of a four-year-old boy with dysmorphic features whose visual examination showed a sudden bilateral loss of vision. There was bilateral eye proptosis and complete ptosis. Extraocular muscles were fixed straight. The pupils were fixed and mid dilated bilaterally and there was grade 3/4 papilledema in both eyes. Neuroimaging showed a mass in the base of the skull, extending to orbits and sinuses. A cervical biopsy of the enlarged lymph nodes was taken and a histopathological diagnosis of Burkitt lymphoma was made. Genetic analysis showed a mutation, and the patient was diagnosed with Kabuki syndrome by a pediatrician, based on characteristic dysmorphic features. Treatment with steroids and chemotherapy was initiated.
伯基特淋巴瘤是一种侵袭性B细胞非霍奇金淋巴瘤(NHL)。原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见疾病,而表现为单纯中枢神经系统病变的伯基特淋巴瘤亚型诊断更为罕见。急性突然失明总体上是PCNSL或NHL罕见的首发症状。我们报告一例有趣的病例,一名4岁男孩有畸形特征,视力检查显示双眼突然失明。双眼眼球突出且完全上睑下垂。眼外肌固定于直视位。双侧瞳孔固定且中度散大,双眼均有3/4级视乳头水肿。神经影像学检查显示颅底有一肿块,延伸至眼眶和鼻窦。对肿大的淋巴结进行了颈部活检,组织病理学诊断为伯基特淋巴瘤。基因分析显示有一个突变,基于特征性畸形特征,儿科医生诊断该患者患有歌舞伎综合征。开始使用类固醇和化疗进行治疗。