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Cutaneous Anaplastic Large T-Cell Lymphoma with Invasion of the Central Nervous System: A Case Reportopen access

Authors
Seo, Hyun-NamSeo, Jin-HoLee, Cheol-YoungSong, JihyeKim, Jong-HyunKim, Hyun-Woo
Issue Date
Apr-2017
Keywords
Lymphoma; Meningioma; Neurofibromatosis
Citation
Brain tumor research and treatment, v.5, no.1, pp 45 - 48
Pages
4
Journal Title
Brain tumor research and treatment
Volume
5
Number
1
Start Page
45
End Page
48
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/74014
DOI
10.14791/btrt.2017.5.1.45
ISSN
2288-2405
2288-2413
Abstract
Anaplastic large T-cell lymphoma (ALCL) encompasses different clinical entities that can be aggressive or localized. Scalp anaplastic lymphoma kinase (ALK)-negative ALCL is considered a localized lymphoma, and usually extends to the regional lymph nodes; intracranial invasion is rare. A 74-year-old woman was diagnosed with scalp ALK-negative ALCL, but did not exhibit invasion of the lymph nodes. Computed tomography and magnetic resonance imaging revealed intracranial masses with bony erosions. We treated the patient using CHOP chemotherapy and achieved short-term regression of the scalp and intracranial lesions. However, the patients ultimately died of pneumonia during the pancytopenic period. Therefore, caution must be exercised when treating scalp ALK-negative ALCL with intracranial invasion.
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