نتایج جستجو برای: thalassemia intermedia

تعداد نتایج: 23663  

2013
NM Nouri M Naderi S Rajaie A Dorgalaleh Sh Tabibian

BACKGROUND Thalassemia intermedia is a variety of beta thalassemia which shows clinical symptoms somewhere between asymptomatic carriers and thalassemia major. Cardiac dysfunctions due to chronic anemia and hemosiderosis are the major causes of death in these patients. The purpose of this study is to evaluate cardiac function in these patients by echocardiography. MATERIALS AND METHODS This c...

2014
Antonella Meloni Maria Eliana Lai Stefania Vacquer Maddalena Lendini Petra Keilberg Maria Chiara Resta Claudio Ascioti Vincenzo Positano Massimo Lombardi Alessia Pepe

Results One-hundred and eighty-eight (74.6%) patients showed no MIO in any segment, 56 (22%) had an heterogeneous distribution (52 with global heart T2*≥20 ms), and 8 (0.3%) showed an homogeneous MIO. Left ventricular (LV) and right ventricular (RV) dilatations were present in 113 (45%) and in 49 (19%) patients, respectively. LV dysfunction was present in the 18.0% of the cases while RV dysfunc...

2010
Qurat-ul-Ain Laiq Ahmad Muhammad Hassan Shahid Mahboob Rana Farhat Jabeen

A cross sectional study was carried out at various hospitals of Faisalabad city. The aim of current study was to investigate the prevalence of β-thalassemia disease in hospital population related to age, consanguinity and anti-HCV antibody positivity. For this purpose, 300 patients were interviewed for the different parameters including specific type of β-thalassemia disease, their family histo...

Journal: :Clinical and laboratory haematology 1988
P R Smith D L Manjoney J B Teitcher K N Choi A S Braverman

We report the case of a 49-year-old woman with thalassemia intermedia who developed a massive hemothorax due to hemorrhage from a large intrathoracic, paraspinal hematopoietic mass. Thoracotomy was required for initial control of bleeding. Postoperatively she received a total of 1,500 rads to the mass and has not had recurrence of the hemothorax. This complication of extramedullary hematopoiesi...

2009
ELENA FABBRI

Patients with thalassemia major, intermedia or double eterozygous with sickle cell disease are exposed to a major risk of developing hepatocellular carcinoma (HCC). Transfusion-transmitted viral infections and long standing iron overload represent principal carcinogenic risk factors. Every effort should be made to prevent tumor development, whose prognosis is usually dismal, or at least to make...

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