scholarly journals Extranodal natural killer/T-cell lymphoma nasal type with central nervous system involvement mimicked tuberculous meningitis

Medicine ◽  
2019 ◽  
Vol 98 (34) ◽  
pp. e16747
Author(s):  
Yina Yang ◽  
Zhouling Li ◽  
Chen Zhiyang ◽  
Hui Liang
2021 ◽  
Vol 69 (4) ◽  
pp. 103313
Author(s):  
Lorenzo Lazzari ◽  
Francesca Farina ◽  
Maria Teresa Lupo Stanghellini ◽  
Simona Piemontese ◽  
Sarah Marktel ◽  
...  

2018 ◽  
Vol 120 ◽  
pp. 17-26 ◽  
Author(s):  
Jiaqi Yan ◽  
Weiping Liu ◽  
Xichuan Wang ◽  
Sha Zhao ◽  
Limin Gao ◽  
...  

2021 ◽  
pp. 014556132098764
Author(s):  
Anthony N. Eze ◽  
Adedoyin O. Kalejaiye

Extranodal natural killer (NK)/T-cell lymphoma, nasal type (NNKTL) is a rare and highly aggressive non-Hodgkin lymphoma originating from NK or γδ T cells infected by Epstein-Barr virus (EBV). In the United States, NNKTL is usually noted in people of Asian or Hispanic descent. Natural killer/T-cell lymphoma, nasal type commonly involves the upper aerodigestive tract, including the nasopharynx, nasal cavity, Waldeyer’s ring, and oropharynx. Extensive local destruction and invasion has been noted, especially of the paranasal sinuses, hard palate, and central nervous system; involvement of the nasolacrimal duct with dacryocystitis is yet to be reported. We report a rare case of a Hispanic man with extranodal NNKTL masquerading as persistent dacryocystitis and necrotizing sinusitis unresponsive to antibiotics and surgical intervention. An extensive background of necrosis and inflammation was noted on pathology, and additional analysis with immunohistochemistry and in situ hybridization after repeat biopsy were necessary for accurate diagnosis.


2014 ◽  
Vol 56 (4) ◽  
pp. 1154-1156 ◽  
Author(s):  
Jianlan Xie ◽  
Xiaoge Zhou ◽  
Xiaojing Zhang ◽  
Yuanyuan Zheng ◽  
Bing Yue

Author(s):  
Tracy T. Batchelor ◽  
Lim Soon Thye ◽  
Thomas M. Habermann

Primary central nervous system lymphoma, natural killer T-cell lymphoma nasal type, and post-transplant lymphoproliferative disorder are uncommon and complex lymphoproliferative disorders. These disorders present with different risk factors, have complex tumor characteristics, and require unique therapeutic interventions. These diseases require a multidisciplinary complex team approach. This article will update current management approaches and concepts.


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