Ghannam Malik, Mansour Shaden, Jumah Fareed, Berry Brent, Beard Albertine
Department of Neurology, University of Minnesota, Minneapolis, MN, USA.
An-Najah National University, Nablus, West Bank, Palestine.
J Med Case Rep. 2018 Nov 17;12(1):341. doi: 10.1186/s13256-018-1880-z.
Primary central nervous system lymphoma is a rare, malignant non-Hodgkin lymphoma that can arise in the brain, spinal cord, eye, leptomeninges, or cranial nerves. Primary central nervous system lymphoma is rare, accounting for 2-6% of all primary brain neoplasms and 1-2% of all non-Hodgkin lymphomas, and it usually presents as a solitary lesion. Cerebellar involvement is present in only 9% of cases. We present an unusual case of primary central nervous system lymphoma presenting as multiple lesions in the cerebellum in an immunocompetent host.
A 71-year-old Caucasian man presented to our hospital with acute onset of dizziness, nausea, vomiting, and gait imbalance. Contrast-enhanced computed tomography revealed three intensely enhancing masses in the right cerebellar hemisphere. Whole-body positron emission tomography and computed tomography failed to demonstrate a primary tumor of origin outside the central nervous system. The patient underwent right suboccipital craniotomy with partial resection of the visible tumor from the right cerebellum. Histopathology revealed diffuse large B-cell lymphoma, non-germinal center type.
Primary central nervous system lymphoma is rare, even more so in the cerebellum. However, the overall incidence of primary central nervous system lymphoma is rising in both immunocompromised and immunocompetent patients. The highly aggressive nature of primary central nervous system lymphoma necessitates timely diagnosis and intervention. In this report, we review the available literature for a better understanding of the pathophysiology and management of primary central nervous system lymphoma. To the best of our knowledge, this is the first reported case of a patient with primary central nervous system lymphoma presenting with multiple masses in the cerebellum.
原发性中枢神经系统淋巴瘤是一种罕见的恶性非霍奇金淋巴瘤,可发生于脑、脊髓、眼、软脑膜或颅神经。原发性中枢神经系统淋巴瘤较为罕见,占所有原发性脑肿瘤的2% - 6%,所有非霍奇金淋巴瘤的1% - 2%,通常表现为单个病灶。仅9%的病例累及小脑。我们报告一例免疫功能正常宿主中表现为小脑多发病灶的原发性中枢神经系统淋巴瘤的罕见病例。
一名71岁的白人男性因急性起病的头晕、恶心、呕吐和步态失衡入院。增强计算机断层扫描显示右小脑半球有三个明显强化的肿块。全身正电子发射断层扫描和计算机断层扫描未发现中枢神经系统以外的原发肿瘤。患者接受了右枕下开颅手术,部分切除了右小脑可见的肿瘤。组织病理学显示为弥漫性大B细胞淋巴瘤,非生发中心型。
原发性中枢神经系统淋巴瘤罕见,在小脑更为少见。然而,原发性中枢神经系统淋巴瘤在免疫功能低下和免疫功能正常的患者中的总体发病率均在上升。原发性中枢神经系统淋巴瘤的高度侵袭性需要及时诊断和干预。在本报告中,我们回顾现有文献以更好地了解原发性中枢神经系统淋巴瘤的病理生理学和治疗方法。据我们所知,这是首例报告的原发性中枢神经系统淋巴瘤患者表现为小脑多发肿块的病例。