Hairy cell leukaemia complicated by anti-MAG paraproteinemic demyelinating neuropathy: resolution of neurological syndrome after cladribrine treatment

Davide Rossi, Silvia Franceschetti, Michaela Cerri, Annarita Conconi, Monia Lunghi, Daniela Capello, Roberto Cantello, Gianluca Gaidano

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Hairy cell leukaemia (HCL) occasionally displays a monoclonal gammopathy, yet the association of HCL with paraproteinemic demyelinating neuropathy (PDN) has not been reported. We describe a HCL case complicated by PDN and high titers of monoclonal IgM against myelin associated glycoprotein (MAG). Heavy and light chains of the patient's anti-MAG monoclonal protein were consistent with those expressed by HCL cells. After treatment with cladribrine, remission of HCL strictly paralleled disappearance of the IgM monoclonal protein and of the serum anti-MAG activity, and led to PDN clinical and electrophysiological improvement. Purine analogs may represent a choice in IgM PDN associated with lymphoproliferative disorders.

Lingua originaleInglese
pagine (da-a)873-876
Numero di pagine4
RivistaLeukemia Research
Volume31
Numero di pubblicazione6
DOI
Stato di pubblicazionePubblicato - giu 2007

Fingerprint

Entra nei temi di ricerca di 'Hairy cell leukaemia complicated by anti-MAG paraproteinemic demyelinating neuropathy: resolution of neurological syndrome after cladribrine treatment'. Insieme formano una fingerprint unica.

Cita questo