Bing-Neel Syndrome – A Challenging Diagnosis: Case Report

Y. Davidkova *

Laboratory of Hematopathology and Immunology, National Specialized Hospital for Active Therapy of Hematological Diseases, Sofia, Bulgaria.

N. Simonoski

Department of Hematology, National Specialized Hospital for Active Therapy of Hematological Diseases, Sofia, Bulgaria.

B. Spassov

Department of Hematology, National Specialized Hospital for Active Therapy of Hematological Diseases, Sofia, Bulgaria.

G. Balatzenko

Laboratory of Medical Genetics, National Specialized Hospital for Active Therapy of Hematological Diseases, Sofia, Bulgaria.

M. Guenova

Laboratory of Hematopathology and Immunology, National Specialized Hospital for Active Therapy of Hematological Diseases, Sofia, Bulgaria.

*Author to whom correspondence should be addressed.


Abstract

Bing-Neel syndrome is a rare neurologic complication of Waldenström’s macroglobulinemia, characterized by infiltration of the central nervous system by clonal lymphoplasmacytes. We present a rare clinical case of a patient, who one year after the diagnosis of Waldenström’s macroglobulinemia, progressed with diverse neurologic presentation and cerebrospinal fluid involvement. The diagnosis was based on magnetic resonance imaging and flow cytometry detection of clonal B-cells in the cerebrospinal fluid. Bing-Neel syndrome should be considered in patients with neurologic symptoms and a history of Waldenström’s macroglobulinemia.

Keywords: Bing-Neel syndrome, Waldenström’s macroglobulinemia, orbital involvement, cerebrospinal fluid.


How to Cite

Davidkova, Y., N. Simonoski, B. Spassov, G. Balatzenko, and M. Guenova. 2020. “Bing-Neel Syndrome – A Challenging Diagnosis: Case Report”. International Blood Research & Reviews 11 (3):28-33. https://doi.org/10.9734/ibrr/2020/v11i330132.

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