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1.
Eur Rev Med Pharmacol Sci ; 19(15): 2798-803, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26241532

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate the usefulness of diffusion-weighted magnetic resonance imaging (DWMRI) for differentation between Graves' disease and Hashimoto's thyroiditis. PATIENTS AND METHODS: Fifty patients (27 Graves diseases and 23 Hashimoto thyroiditis) and twenty healthy volunteers were examined using T1, T2 and DWMRI. The patients were diagnosed on the basis of physical findings and the results of thyroid function tests and serological tests. Circular ROIs were positioned on the bilateral thyroid lobes and isthmus. All measurements were repeated three different b values including 100, 600 and 1000 s/mm2 in all cases. ADC (Apparent diffusion coefficient) maps were calculated automatically with the MR system. RESULTS: Mean ADC values were 2.93 × 10-3, 1.97 × 10-3 and 1.62 × 10-3 mm2/s in the healthy volunteers; 3.47 × 10-3, 2.25 × 10-3 and 1.64 × 10-3 mm2/s in Graves' disease; 2.53 × 10-3, 1.76 × 10-3, 1.28 × 10-3 mm2/s in Hashimoto thyroiditis for b100, b600 and b1000, respectively. The ADC values of the Graves diseases were higher than healty volunteers and Hashimoto thyroiditis. ADC values were statistically significant for differentation between Hashimoto thyroiditis and Graves' disease all b values (p < 0.05). CONCLUSIONS: DWMRI is fast sequence and does not require contrast agent. Quantitative assessment of the lesion is possible using ADC map. So, DWMRI may be useful differentiation of the Hashimoto thyroiditis and Graves' disease.


Subject(s)
Diffusion Magnetic Resonance Imaging/methods , Graves Disease/diagnostic imaging , Hashimoto Disease/diagnostic imaging , Thyroid Function Tests/methods , Adult , Aged , Female , Graves Disease/diagnosis , Hashimoto Disease/diagnosis , Humans , Male , Radiography
4.
Turk J Pediatr ; 40(4): 613-8, 1998.
Article in English | MEDLINE | ID: mdl-10028874

ABSTRACT

Holt-Oram syndrome is a distinct autosomal dominant entity presenting with upper limb defects and cardiac abnormality. No correlation between the severity of the heart and the limb defects has been established. Here we report variable clinical expression of Holt-Oram syndrome in three generations. The grandfather presented with typical upper limb defects: phocomelia of arms with three digits on each hand, congenital heart defect and narrow shoulders. His son manifested cardiac conduction disturbance with no congenital heart or skeletal defect. The granddaughter showed ventricular septal defect and moderate radial deviations of both hands with no obvious hypoplasia of the extremities. Clinical data of the presented family suggests lack of penetrance with respect to skeletal and structural cardiac abnormalities in the Holt-Oram syndrome.


Subject(s)
Ectromelia/genetics , Heart Block/genetics , Heart Defects, Congenital/genetics , Female , Humans , Infant, Newborn , Male , Middle Aged , Pedigree , Penetrance , Syndrome
6.
Prenat Diagn ; 15(5): 477-81, 1995 May.
Article in English | MEDLINE | ID: mdl-7644439

ABSTRACT

Prenatal diagnosis for infantile osteopetrosis was attempted during the third pregnancy of a first-cousin marriage whose family history revealed an affected previous child. At the 25th week of pregnancy, fetal X-ray evaluation revealed marked sclerosis of osteopetrotic bone and metaphyseal splaying and clubbing of both femurs. The pregnancy was terminated and repeated X-rays and histopathological examination of fetal bone (femur) confirmed the diagnosis.


Subject(s)
Osteopetrosis/diagnostic imaging , Prenatal Diagnosis , Abortion, Induced , Consanguinity , Female , Femur/pathology , Fetal Diseases/diagnostic imaging , Humans , Male , Osteopetrosis/pathology , Pedigree , Pregnancy , Radiography
7.
Ann Anat ; 177(1): 89-92, 1995 Jan.
Article in English | MEDLINE | ID: mdl-7872501

ABSTRACT

During the dissection of the neck region of a 56 year old female cadaver an artery was found branching from the thyrocervical trunk as a fourth branch and entering the aortic arch on its superior posterior aspect between the brachiocephalic trunk and the left common carotid artery. Selective angiography revealed that this artery branched into several arterioles at its junction on the superior aspect of the aortic arch between the brachiocephalic trunk and the left common carotid artery. No similar structure could be found in the literature. Evaluation of this phenomenon according to our knowledge of the development of human arterial networks, it was concluded that the artery might be a persistent intersegmental artery, or an enlarged nutrient artery (vas vasorum) to the aortic arch.


Subject(s)
Aorta, Thoracic/anatomy & histology , Arteries/anatomy & histology , Arterioles/anatomy & histology , Aged , Angiography , Aorta, Thoracic/diagnostic imaging , Aorta, Thoracic/embryology , Arteries/embryology , Arteries/pathology , Arterioles/diagnostic imaging , Arterioles/pathology , Cadaver , Embryo, Mammalian , Female , Humans
8.
Paraplegia ; 31(9): 606-10, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8247603

ABSTRACT

In this study to determine the incidence of deep vein thrombosis (DVT) in spinal cord injury (SCI) patients, we evaluated 30 instances of bilateral ascending venography obtained in 31 patients. Every patient was on prophylactic low dose heparin anticoagulant therapy. The incidence of DVT was found to be 53.3%. Adverse effects due to venography were seen in 10% of patients. No major complications including postvenographic phlebitis and allergic reactions were observed.


Subject(s)
Spinal Cord Injuries/complications , Thrombophlebitis/etiology , Adult , Female , Heparin/therapeutic use , Humans , Male , Middle Aged , Muscle Spasticity/complications , Phlebography/adverse effects , Pulmonary Embolism/complications , Thrombophlebitis/diagnosis , Thrombophlebitis/drug therapy
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