Article
[IgG-variant Bing-Neel syndrome diagnosed by detecting MYD88 L265P mutation in the cerebrospinal fluid cells].
[Rinsho ketsueki] The Japanese journal of clinical hematology - 1 Jan 2021
Maruyama Yumiko, Nishikii Hidekazu, Matsuoka Ryota, Makishima Kenichi, Kurita Naoki, Kusakabe Manabu, Yokoyama Yasuhisa, Kato Takayasu, Sakata-Yanagimoto Mamiko, Obara Naoshi, Nakamura Naoya, Chiba Shigeru
Abstract excerpt
Bing-Neel syndrome (BNS), which presents with a variety of neurological complications, is a rare manifestation of the lymphoplasmacytic lymphoma (LPL) and is characterized by the infiltration of LPL cells into the central nervous system. In this study, we report the case of a patient with BNS, which was confirmed by detecting MYD88 L265P mutation in the cerebrospinal fluid (CSF) cells. A 74-year-old patient was...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.