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Initial lymphocyte count and the development of persistent/chronic immune thrombocytopenic purpura

dc.contributor.authorAhmed, Ibrahimen_US
dc.contributor.authorRajpurkar, Madhvien_US
dc.contributor.authorThomas, Ronalden_US
dc.contributor.authorChitlur, Meera B.en_US
dc.date.accessioned2010-08-02T17:48:47Z
dc.date.available2011-03-01T16:26:42Zen_US
dc.date.issued2010-09en_US
dc.identifier.citationAhmed, Ibrahim; Rajpurkar, Madhvi; Thomas, Ronald; Chitlur, Meera (2010). "Initial lymphocyte count and the development of persistent/chronic immune thrombocytopenic purpura." Pediatric Blood & Cancer 55(3): 508-511. <http://hdl.handle.net/2027.42/77530>en_US
dc.identifier.issn1545-5009en_US
dc.identifier.issn1545-5017en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/77530
dc.description.abstractBackground Acute immune thrombocytopenic purpura (ITP) is a common, benign, self-limiting disease in children. Chronic ITP is diagnosed when thorombocytopenia persists beyond 12 months. Older age is associated with increased risk for development of chronic ITP. The main objective of the current study was to examine whether total leukocyte (TLC) and absolute lymphocyte counts (ALC) at diagnosis correlate with the persistence of ITP beyond 6 months. Procedure Two hundred and twenty four consecutive medical records for patients diagnosed with immune thrombocytopenia, between April 1993 and July 2007, were reviewed and 188 patients were eligible for analysis. Case records were examined to ascertain the following information: age, gender, ethnicity, date of presentation, presenting CBC with differential count, treatment given and the outcome. Results The male to female ratio was almost 1:1; 24% (45/188) of patients had persistent ITP beyond 6 months. We determined that age >8.5 year, TLC < 6,250/µl and ALC < 3,050/µl was associated with a significant risk for development of persistent ITP beyond 6 months. Conclusions TLC and ALC at diagnosis are predictive variables for the development of persistent/chronic ITP. Further studies are recommended to confirm the current finding and to assess the underlying pathophysiology with the course of the ITP. Pediatr Blood Cancer. 2010;55:508–511. © 2010 Wiley-Liss, Inc.en_US
dc.format.extent120514 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleInitial lymphocyte count and the development of persistent/chronic immune thrombocytopenic purpuraen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationotherThe Carman and Ann Adams Department of Pediatrics, Pediatric Hematology/Oncology Division, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan ; Pediatric Oncology Division, National Cancer Institute, Cairo University, Cairo, Egypt ; Pediatric Oncology Division, National Cancer Institute, Cairo University, Foum El-Khalig, Kasr Al-Aini, Cairo, Egypt.en_US
dc.contributor.affiliationotherThe Carman and Ann Adams Department of Pediatrics, Pediatric Hematology/Oncology Division, Children's Hospital of Michigan, Wayne State University, Detroit, Michiganen_US
dc.contributor.affiliationotherChildren's Research Center of Michigan, Wayne State University, Detroit, Michiganen_US
dc.contributor.affiliationotherThe Carman and Ann Adams Department of Pediatrics, Pediatric Hematology/Oncology Division, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan ; Children's Hospital of Michigan, Pediatric Hematology Oncology Division, 3901 Beaubien Blvd, Detroit, MI 48201.en_US
dc.identifier.pmid20658623en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/77530/1/22570_ftp.pdf
dc.identifier.doi10.1002/pbc.22570en_US
dc.identifier.sourcePediatric Blood & Canceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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