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[Bing-Neel syndrome successfully treated with tirabrutinib]

Authors :
Keito, Yokoyama
Hiroyuki, Ohigashi
Toru, Miyajima
Naoki, Miyashita
Satomi, Okada
Yuta, Hasegawa
Junichi, Sugita
Masahiro, Onozawa
Daigo, Hashimoto
Takanori, Teshima
Source :
[Rinsho ketsueki] The Japanese journal of clinical hematology. 63(8)
Publication Year :
2022

Abstract

Bing-Neel syndrome (BNS) is a rare disease manifestation of Waldenström's macroglobulinemia characterized by abnormal lymphoplasmacytoid cells infiltration of the central nervous system. In September 2019, a 46-year-old man presented to a previous hospital with hand tremors, nausea, and dysuria. Demyelination of cerebral white matter and the spinal cord was discovered using MRI. Steroid pulse therapy was used to treat inflammatory demyelinating disease, and it provided temporary relief, but the symptoms returned when the steroids were stopped. He was referred to our hospital in June 2020, for further evaluation with the possibility of hematological malignancy. BNS was diagnosed based on the presence of abnormal lymphoplasmacytoid cells in the bone marrow and cerebrospinal fluid (CSF), as well as the presence of the MYD88

Details

ISSN :
04851439
Volume :
63
Issue :
8
Database :
OpenAIRE
Journal :
[Rinsho ketsueki] The Japanese journal of clinical hematology
Accession number :
edsair.pmid..........111fdedc224010df0d0ee6838ccdc88f