Literature DB >> 18454893

Diagnostic tool for Glanzmann's thrombasthenia clinicopathologic spectrum.

Natasha Ali1, Bushra Moiz, Usman Shaikh, Salman Adil, Bushra Rizvi, Yasmeen Rahman.   

Abstract

OBJECTIVE: To platelet aggregometry and describe the clinical spectrum of Glanzmann's thrombasthenia diagnosed by platelet aggregometry. STUDY
DESIGN: A case-series. PLACE AND DURATION OF STUDY: This study was carried out at the clinical laboratories at the Aga Khan University Hospital, Karachi from January 2003 to January 2006. PATIENTS AND METHODS: All patients irrespective of age and gender presenting with bleeding symptoms and having normal platelet count were evaluated. Demographic details, relevant clinical history along with results of complete blood count, bleeding time and platelet aggregation studies were retrieved through computerized data base and evaluated for the diagnosis of Glanzmann's thrombasthenia.
RESULTS: During the study period, 50 out of 2317 patients (2.2%) were diagnosed as Glanzmann's thrombasthenia by platelet aggregometry with male to female ratio of 0.85:1 and median age of 10.2 years (ranging from 3 months to 27 years). Common symptoms were epistaxis, oral and gingival bleed, bleeding from minor cuts and trauma that were observed in 46% of the patients; while 18%, 8% and 10% of them also complained of bruising, hematuria and bleeding per rectum respectively. Majority i.e. 86% had a bleeding time greater than 10 minutes. All patients had received blood or blood products for their bleeding episodes.
CONCLUSION: Platelet aggregometry is a useful diagnostic modality for the assessment of Glanzmann's thrombasthenia. The disorder presents with muco-cutaneous bleeding and was found to be a common cause of bleeding in our setup.

Entities:  

Mesh:

Year:  2008        PMID: 18454893     DOI: 02.2008/JCPSP.9194

Source DB:  PubMed          Journal:  J Coll Physicians Surg Pak        ISSN: 1022-386X            Impact factor:   0.711


  3 in total

1.  Simultaneous occurrence of intussusception and duodenal haematoma in a patient with Glanzmann's thrombasthenia.

Authors:  Iftikhar Ahmad Jan; Saif Khalfan AlKaabi; Awadh AlMughadam; D Sreenivas Murthy; Basmah AlHamoudi
Journal:  Afr J Paediatr Surg       Date:  2016 Oct-Dec

2.  [Glanzmann thrombasthenia: about 11 cases].

Authors:  Jean-Louis Ntumba Mukendi; Souad Benkirane; Azlarab Masrar
Journal:  Pan Afr Med J       Date:  2015-08-11

3.  Genetic Confirmation and Identification of Novel Variants for Glanzmann Thrombasthenia and Other Inherited Platelet Function Disorders: A Study by the Korean Pediatric Hematology Oncology Group (KPHOG).

Authors:  Eu Jeen Yang; Ye Jee Shim; Heung Sik Kim; Young Tak Lim; Ho Joon Im; Kyung-Nam Koh; Hyery Kim; Jin Kyung Suh; Eun Sil Park; Na Hee Lee; Young Bae Choi; Jeong Ok Hah; Jae Min Lee; Jung Woo Han; Jae Hee Lee; Young-Ho Lee; Hye Lim Jung; Jung-Sook Ha; Chang-Seok Ki
Journal:  Genes (Basel)       Date:  2021-05-06       Impact factor: 4.096

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.