A Rare Case Presentation of HbE/ β Thalassemia
نویسندگان
چکیده
منابع مشابه
Sickle cell-β thalassemia with concomitant hemophilia A: a rare presentation
men and pelvis are essential to stage the disease accurately [12]. Currently, there is a controversy in the reported literature regarding the accuracy of positron-emission tomography-CT scanning of MALTomas. Radical parotidectomy is not indicated because of the associated morbidity, and because RT alone can secure local control and allow tissue preservation. Low dose RT (30 Gy) is extremely eff...
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HbE/β-thalassaemia genotype represent approximately 50% of all severe β-thalassemia worldwide and is the commonest form of thalassemia in many Asian countries, predominantly prevalent in North-Eastern region exhibiting phenotypes that range from severely symptomatic and transfusion-dependent anaemia in early life to a asymptomatic and clinically ‘silent’ condition that is ascertained by chance ...
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Eosinophilic cholecystitis is a rare inflammatory condition encountered in surgical cholecystectomy specimens. In terms of histopathology, it is defined by transmural infiltration of eosinophils composing more than 90% of leukocytes. We here report a case of 19-year-old male admitted with thalassemia intermedia and with severe left upper quadrant pain. The patient underwent open splenectomy and...
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Background: Eβ Thalassemia is characterized by clinical heterogeneity ranging from Non-Transfusion Dependent Thalassemia (NTDT) to Transfusion Dependent Thalassemia (TDT) state, causing management challenges for the clinicians, especially in the pediatric population. Therefore, this study was conducted to give an overview of the clinical profile and management in a tertiary care center. Materi...
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ژورنال
عنوان ژورنال: Annals of Pathology and Laboratory Medicine
سال: 2020
ISSN: 2349-6983,2394-6466
DOI: 10.21276/apalm.2794