Literature DB >> 18029131

Prevalence of hepatosplenomegaly in beta thalassemia minor subjects in Iran.

Mehran Karimi1, Mohammad Hadi Bagheri, Mehdi Tahmtan, Alireza Shakibafard, Murtaza Rashid.   

Abstract

INTRODUCTION: Thalassemia is the most common hereditary blood disorder in the world. Iran is located on the thalassemic belt and there is a high prevalence of the hepatosplenomegaly in beta thalassemia minor patients which is reported to be very variable. The goal of this research was to study the frequency of these signs in the cases with beta thalassemia minor patients in Iran.
MATERIALS AND METHODS: Two hundred and fifty-nine cases that referred to center for pre-marriage tests were divided into two groups according to their MCV, MCH, and HbA2 (beta thalassemia minor cases and control groups). Liver and spleen sizes were determined by ultrasonographic method and the two groups were compared with each other.
RESULTS: Average spleen volumes in case and control groups were 163.48+/-133.97 and 126.29+/-53.98mm(3), respectively. Average spleen lengths in case and control groups were 10.71+/-1.52 and 10.60+/-5.4cm, respectively.
CONCLUSION: In the regions with high frequency of beta thalassemia, in case of finding large spleen size in the ultrasonography, a probable harmless differential diagnosis will be beta thalassemia minor that is not indicative of any serious disease. Volumetric measurement of spleen is more reliable for detection of splenomegaly in these patients.

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Year:  2007        PMID: 18029131     DOI: 10.1016/j.ejrad.2007.09.027

Source DB:  PubMed          Journal:  Eur J Radiol        ISSN: 0720-048X            Impact factor:   3.528


  5 in total

1.  Symphysis morphology and mandibular alveolar bone thickness in patients with β-thalassemia major and different growth patterns.

Authors:  Leila Khojastepour; Atefe Naderi; Fatemeh Akbarizadeh; Najmeh Movahhedian; Farzaneh Ahrari
Journal:  Dental Press J Orthod       Date:  2022-05-23

2.  Coincidence of Niemann-Pick Disease and beta-Thalassemia; a Case Report.

Authors:  Fatemeh Farahmand; Vajiheh Modaresi; Mina Izadyar; Fatemeh Mahjob
Journal:  Iran J Pediatr       Date:  2010-12       Impact factor: 0.364

3.  Ultrasonographic assessment of splenic volume and its correlation with body parameters in a Jordanian population.

Authors:  Darwish H Badran; Heba M Kalbouneh; Maher T Al-Hadidi; Amjad T Shatarat; Emad S Tarawneh; Azmy M Hadidy; Waleed S Mahafza
Journal:  Saudi Med J       Date:  2015-08       Impact factor: 1.484

Review 4.  Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area.

Authors:  Mohamad H Qari; Yasser Wali; Muneer H Albagshi; Mohammad Alshahrani; Azzah Alzahrani; Ibrahim A Alhijji; Abdulkareem Almomen; Abdullah Aljefri; Hussain H Al Saeed; Shaker Abdullah; Ahmad Al Rustumani; Khoutir Mahour; Shaker A Mousa
Journal:  Orphanet J Rare Dis       Date:  2013-09-17       Impact factor: 4.123

5.  The Incidence of Minor β-thalassemia Among Individuals Participated in Premarital Screening Program in Ardabil Province: North-west of Iran.

Authors:  Afshin Fathi; Firouz Amani; Nahaleh Mazhari
Journal:  Mater Sociomed       Date:  2019-12
  5 in total

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