• Passa alla navigazione primaria
  • Passa al contenuto principale
BC

biochimica clinica

it_IT Italian
it_IT Italian en_US English
  • Home
  • Casi clinici
  • Ahead of print e Ultimo Fascicolo - Accedi per visualizzare gli articoli
  • Archivio BC fino a 2024
  • Sottometti un articolo
  • Norme Autori
  • Cerca

CASI CLINICI – Case Reports

Volume:

Biochimica Clinica 2019; 43(4) e38-e40

Pubblicato on-line:

Ottobre 15, 2019

DOI:

10.19186/BC_2019.062

Scarica in PDF:
Autenticazione richiesta

Un caso clinico di linfocitosi persistente

AUTORI

Blerina Jance1, Benedetta Salvadori1, Francesca Cesari1, Angela Rogolino1, Benedetta Peruzzi2, Roberto Caporale2, Alessandra Fanelli1
1Laboratorio Generale, Azienda Ospedaliero-Universitaria Careggi, Firenze
2Centro diagnostico di Citometria e Immunoterapia, Azienda Ospedaliero-Universitaria Careggi, Firenze

ABSTRACT

Persistent Lymphocytosis

Persistent Polyclonal Binucleated B-cell Lymphocytosis (PPBL) is a rare, benign hematological disorder characterized by a chronic polyclonal B-cell lymphocytosis with binucleated lymphocytes. We report the clinical case of a young woman with lymphocytosis who presented binucleate lymphocytes at the morphological examination of the peripheral venous blood smear. Flow cytometry immunophenotyping performed in peripheral blood showed a polyclonal lymphocyte B subpopulation. Serological tests were negative for viral infections. Because of its benign and indolent course, the diagnoses of PPBL is important in order to avoid unnecessary diagnostic procedures and therapies.

BIBLIOGRAFIA