Document Detail


From neonates to adolescents--the diagnostic significance of pitted erythrocytes in hyposplenic and asplenic children.
MedLine Citation:
PMID:  18050044     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Splenic function may be reduced or absent in a range of medical conditions in childhood, most prominently in homozygous sickle cell disease, celiac disease, or after total or partial splenectomy. In neonates and patients with malignant disease, transient hyposplenia has been reported as well. A simple method with reliable reference values is required to determine a patient's splenic function and thereby assess the risk of systemic infection. PATIENTS: Pitted erythrocytes (pitE) were determined semi-quantitatively in patients up to 20 years of age. This included splenectomized individuals, patients at risk for hyposplenia (homozygous sickle cell anemia (HbSS), leukemia, nephroblastoma and Hodgkin's disease after irradiation, patients after stem cell transplantation (SCT)), term and preterm neonates, and 90 controls (0-20 years of age, no neonates). METHOD: A capillary blood sample was diluted in buffered glutaraldehyde. PitE were scored using differential interference contrast microscopy with Nomarski optics. RESULTS: PitE were <2% in all controls regardless of age, in splenectomized individuals >18%. In patients with HbSS, pitE scores ranged from 6.2 to 44%. Scores did not exceed 2% in patients after SCT, irradiation, or during chemotherapy for leukaemia. In term neonates, pitE were increased in the perinatal period only. The elevation in preterm neonates persisted up to 2 months after birth. CONCLUSION: Serial measurement of pitE can be used to accurately and reliably assess splenic function in children. Except for neonates, pitE are consistently <2% in healthy individuals. For clinical purposes, the degree of hyposplenia can be determined to give an estimation of the risk of severe infection, e.g. in patients with HbSS or after partial splenectomy.
Authors:
K Lehmberg; B Steinhausen; G Janka
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Publication Detail:
Type:  Comparative Study; Evaluation Studies; Journal Article    
Journal Detail:
Title:  Klinische Pädiatrie     Volume:  219     ISSN:  0300-8630     ISO Abbreviation:  Klin Padiatr     Publication Date:    2007 Nov-Dec
Date Detail:
Created Date:  2007-11-30     Completed Date:  2008-02-25     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0326144     Medline TA:  Klin Padiatr     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  339-42     Citation Subset:  IM    
Affiliation:
Department of Paediatric Haematology and Oncology, Children's Hospital, University of Hamburg, Hamburg. k.lehmberg@uke.uni-hamburg.de
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Anemia, Sickle Cell / diagnosis*,  genetics
Child
Child, Preschool
Erythrocytes, Abnormal*
Homozygote
Humans
Infant
Infant, Newborn
Microscopy, Interference
Reproducibility of Results
Spleen / physiology*
Splenectomy*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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