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cardiomegaly/edema
Veza se sprema u međuspremnik
Stranica 1 iz 438 rezultatima
Antenatal diagnosis of large sacro-coccygeal teratoma with foetal cardiomegaly and hydrops.
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We report the case of a young primigravida who presented with a 20 weeks pregnancy with a previous diagnosis of uterine fibroid. However, ultrasound evaluation revealed the presence of a large sacro-coccygeal teratoma in the foetus which was heterogeneous with cystic areas and calcific foci, and
Isolated cardiomegaly in the second trimester as an early sign of fetal hydrops due to intracranial arteriovenous malformation.
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We report the case of a 27-year-old pregnant woman in whom isolated mild fetal cardiomegaly, diagnosed prenatally on sonographic examination at 22 weeks' menstrual age, was the first sign of development of an arteriovenous malformation of the vein of Galen. The arteriovenous malformation was
Pulmonary edema in coronary-artery disease without cardiomegaly. Paradox of the stiff heart.
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Pulmonary edema without cardiomegaly.
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Clinicopathological conference. Marked edema, wheezing and cardiomegaly.
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A Young Man With Cardiomegaly and Edema.
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Pulmonary edema without cardiomegaly: ischemic cardiomyopathy and the small stiff heart.
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Clinicopathologic conference: pulmonary edema, cardiomegaly, and anemia.
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Edema and heart failure without cardiomegaly.
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WEEKLY clinicopathological exercises: isolated myocarditis, idiopathic cardiac hypertrophy, with mural thrombus of left ventricle; hemorrhagi pulmonary edema, severe.
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Chronic nasopharyngeal obstruction as a cause of cardiomegaly, cor pulmonale, and pulmonary edema.
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Two unusual cases of haemoglobin Bart's hydrops fetalis due to uniparental disomy or non-paternity.
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The authors present 2 unusual cases of haemoglobin (Hb) Bart's hydrops fetalis and highlight the problem of a screening system for α-thalassaemia which focuses on maternal and paternal mean corpuscular volume (MCV) alone. Normal paternal MCV may not preclude fetal Hb Bart's disease because of the
Is the ultrasound definition of fluid collections in non-immune hydrops fetalis helpful in defining the underlying cause or predicting outcome?
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The ultrasound findings in 132 patients with non-immune hydrops referred for echocardiographic assessment were retrospectively reviewed. Structural assessment was combined with evaluation of pleural and pericardial effusions, ascites and skin edema. Patients were divided into groups based on the
An increase of the cardiothoracic ratio leads to a diagnosis of Bart's hydrops.
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BACKGROUND
Thalassemia is a common single gene disorder in Southeast Asia. a-thalassemia is a group of syndrome characterized by deficient production of the alpha-globin chain. Individuals with heterozygous alpha-thalassemia-1 are at risk of having a fetus that has Hemoglobin Bart's hydrops fetalis
Noncardiogenic pulmonary edema as the first manifestation of pheochromocytoma: a case report.
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We report here a case of pheochromocytoma presenting with noncardiogenic pulmonary edema, which is an unusual first manifestation of pheochromocytoma. Chest radiograph showed diffuse consolitaion and ground-glass opacity on both lungs. Neither pleural effusion nor cardiomegaly was present.
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