A Rare Clinical Case of Secondary Central Nervous System Involvement without Transformation in Hairy Cell Leukemia: Case Report and Literature Review

被引:1
|
作者
Ito, Kenichi [1 ]
Harada, Kunihiko [2 ]
Uchino, Yoshihito [1 ]
Hirano, Kazuhiko [2 ]
Sekiguchi, Naohiro [1 ,3 ,4 ]
机构
[1] Natl Hosp Org Disaster Med Ctr, Hematol Div, Tokyo, Japan
[2] Natl Hosp Org Disaster Med Ctr, Lab & Pathol Div, Tokyo, Japan
[3] Natl Hosp Org Disaster Med Ctr, Clin Res Div, Tokyo, Japan
[4] Natl Hosp Org Disaster Med Ctr, Hematol Div, 3256 Midori-cho, Tachikawa, Tokyo 1900014, Japan
关键词
hairy cell leukemia; central nervous system involvement; indolent B-cell lymphoma; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; BRAF V600E; RITUXIMAB; DIAGNOSIS; LYMPHOMA; PATIENT; IMMUNOHISTOCHEMISTRY; MENINGITIS; MUTATIONS; THERAPY;
D O I
10.1159/000535066
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionHairy cell leukemia (HCL) is an indolent B-cell lymphoma characterized by a specific genetic mutation, BRAF V600E, which affects the specific morphology and oncogenesis. For HCL, few reports regarding secondary central nervous system involvement (SCNSI) are available. Herein, we present the case of an 80-year-old woman who had a relapse of HCL with SCNSI. Case presentationThe diagnosis of HCL was made in June 2015 after identifying BRAF V600E proteins by immunohistochemical analysis, and the disease was then controlled for 6 years by employing chemoimmunotherapy. In February 2021, the patient was admitted with neurological symptoms such as dizziness. Magnetic resonance imaging of the brain showed abnormal enhancement in the cerebrum, and cerebrospinal fluid analysis revealed neoplastic cells without transformation into large cells. Thus, the patient was diagnosed as having SCNSI in HCL.ConclusionWe report a case of a rare clinical presentation of SCNSI in HCL with literature review.
引用
收藏
页码:482 / 488
页数:7
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