Primary cutaneous CD 30+ T-cell lymphoproliferative disorder presenting as paraphimosis: A case report and review of the literature

2011 ◽  
Vol 17 (7) ◽  
Author(s):  
Patricia Moody McNab ◽  
Drazen M Jukic ◽  
Omie Mills ◽  
Irwin Browarsky
Keyword(s):  
Case Report ◽  
T Cell ◽  
Lymphoproliferative Disorder ◽  
Review Of The Literature

scholarly journals Primary laryngeal T-cell lymphoma: A case report and review of the literature

2021 ◽  
Vol 82 ◽  
pp. 105858
Author(s):  
K. Chaker ◽  
M. Beghdad ◽  
M.A. Mennouni ◽  
A. Mkhatri ◽  
Y. Oukessou ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Review Of The Literature

Primary vitreoretinal natural killer/T-cell lymphoma with breast involvement: A case report and review of the literature

2019 ◽  
Vol 64 (2) ◽  
pp. 225-232 ◽  
Author(s):  
Shuang Gao ◽  
Yingming Zhou ◽  
Xiaolong Jin ◽  
Zhongjing Lin ◽  
Yisheng Zhong ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Natural Killer ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Review Of The Literature ◽  
Natural Killer T Cell ◽  
Killer T Cell ◽  
Natural Killer T

scholarly journals Primary cutaneous CD4+ small/medium T-cell lymphoma: a case report

2021 ◽  
Vol 22 (4) ◽  
pp. 199-203
Author(s):  
Jeenam Kim ◽  
Minkyoung Jeong ◽  
Dongkeun Jun ◽  
Myungchul Lee ◽  
Donghyeok Shin ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Lymphoproliferative Disorder ◽  
Cell Lymphoma ◽  
Surgical Excision ◽  
Lymphoid Cells ◽  
The Face ◽  
Single Mass ◽  
Histopathologic Findings

Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder is a rare disease characterized by a single mass on the face or upper part of the trunk. It usually presents an asymptomatic and favorable progression, and its histopathologic findings include small and medium-sized lymphoid cells. The authors report a case of primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder on the forehead. A 51-year-old man presented with a protruding mass on his forehead that the patient had noted 1 month previously. Surgical excision and a permanent biopsy were performed under local anesthesia. Based on the biopsy results, the mass was diagnosed as a primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder. There was no evidence of recurrence at a 15-month follow-up visit.

Development of hepatosplenic γδ T-cell lymphoma with pancytopenia during early pregnancy: a case report and review of the literature

2004 ◽  
Vol 73 (5) ◽  
pp. 367-371 ◽  
Author(s):  
Nozomi Niitsu ◽  
Mika Kohri ◽  
Tomiteru Togano ◽  
Hirokazu Nakamine ◽  
Shigeo Nakamura ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Early Pregnancy ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Γδ T Cell ◽  
Review Of The Literature

Primary gastric T-cell lymphoma not associated with human T-lymphotropic virus type I: a case report and review of the literature

2003 ◽  
Vol 82 (3) ◽  
pp. 197-202 ◽  
Author(s):  
N. Niitsu ◽  
H. Nakamine ◽  
M. Kohri ◽  
M. Hayama ◽  
J. Tamaru ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Virus Type ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Type I ◽  
Review Of The Literature ◽  
T Lymphotropic Virus

scholarly journals CD20+ cutaneous T-cell lymphoma with phenotypic shift after treatment with rituximab: Case report and review of the literature

2020 ◽  
Vol 6 (4) ◽  
pp. 308-310
Author(s):  
Amanda J. Tschetter ◽  
Faraaz Zafar ◽  
Margaret S. Moye ◽  
Grant K. Ghahramani ◽  
Brian L. Swick ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Cutaneous T Cell Lymphoma ◽  
Review Of The Literature ◽  
Phenotypic Shift
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