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Spectrum of bone marrow failures of myeloid series: new report of neutropenic patients from a referral pediatric center in Iran.

Abstract
Neutropenia is a reduction of the absolute neutrophil count (ANC), which could be seen in different conditions, while its association with a number of primary immunodeficiency diseases has been reported. This study was performed in all neutropenic patients who were admitted in a referral pediatric hospital during a 6-year period (2006-2011). One hundred and forty patients with ANC of below 1500/mm(3) were investigated in this study. The most common causes of neutropenia were severe congenital neutropenia (41%), aplastic anemia (19%), cyclic neutropenia (11%), hyperimmunoglobulin M syndrome (9%), and fanconi anemia (7%). The patients experienced their first manifestation at a median age of 1 year, while the median diagnostic age was 21 months. Parental consanguinity was present in about half of the cases. The most common clinical manifestations of the patients were sinusitis (62 cases), periodontitis (51 cases), acute diarrhea (39 cases), pneumonia (38 cases), abscess (36 cases), skin rashes (35 cases), and otitis media (31 cases). Twenty two patients (16%) died during the study period. Considering the differential diagnosis of neutropenia, making the diagnosis and appropriate treatments are the keys in management of patients with neutropenia to avoid further complications.
AuthorsMohammad Taghi Majnoon, Setareh Mamishi, Kasra Moazzami, Leila Shahbaznejad, Mina Izadyar, Farah Sabouni, Leila Koochakzadeh, Asghar Ramyar, Asghar Aghamohammadi, Nima Rezaei
JournalPediatric hematology and oncology (Pediatr Hematol Oncol) Vol. 31 Issue 2 Pg. 109-16 (Mar 2014) ISSN: 1521-0669 [Electronic] England
PMID23363289 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Adolescent
  • Bone Marrow Diseases (blood, diagnosis)
  • Child
  • Child, Preschool
  • Consanguinity
  • Diagnosis, Differential
  • Female
  • Humans
  • Infant
  • Male
  • Neutropenia (blood, congenital, diagnosis, genetics)

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