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Query: UMLS:C0264733 (ventricular dilatation)
 2,163 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

An echocardiographic and electrocardiographic evaluation of left ventricular hypertrophy (LVH) was carried out in 50 patients with chronic pressure or volume overload of the left ventricle, and in 16 patients with cardiomyopathy. In contrast to the ECG, echocardiography permitted good differentiation of ventricular dilatation, symmetrical and asymmetrical wall thickening. Positive voltage criteria (SOKOLOFF) were found in 76% of cases with abnormal muscle mass, but the height of QRS amplitude showed no close correlation with the degree of LVH. The presence of absence of ST/T changes was an unreliable index in predicting wall thickness. The practical value of echocardiagraphy in the differential diagnosis of left ventricular disorders is discussed.
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PMID:[Proceedings: Echocardiography for the diagnosis of left ventricular hypertrophy]. 12 54

Between 1976 and 1978, we examined 110 Japanese children with cerebral palsy using a CT 1000 and a CT 1010 (EMI). In 92% of all patients, there were abnormal findings. Cortical atrophy was seen in 51%, ventricular dilatation in 86%, localized low density areas in 22%, brain anomalies in 10% and asymmetry of cerebral hemisphere in 31%. In spastic hemiplegia, the characteristic CT revealed asymmetrical ventricular dilatation without cortical atrophy and localized low density areas in the cerebral hemisphere contralateral to the palsy. In spastic tetraplegia, CT revealed moderate to marked diffuse cerebral atrophy or brain anomalies. In athetosis, CT revealed normal or slight cerebral atrophy. In 60 cases where a CT 1010 was used, we calculated the volume index of CSF space by computer, Eclipse S/200, and analyzed the relationship between the clinical features of cerebral palsy and the volume index of CSF space.
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PMID:Computed tomography of cerebral palsy: evaluation of brain damage by volume index of CSF space. 55 48

Serial electrocardiograms as well as echocardiographic studies of 51 pilgrims suffering from acute heat stroke (mean rectal temperature 41.6 degrees C) were performed. All patients were examined immediately after cooling and 24 h later whenever possible. Regional wall motion abnormalities were detected in 9 cases (17.6%) while pericardial effusion was observed in 13 cases (25%) and asymmetrical septal hypertrophy was detected in 8 cases (15.6%). Other cardiac abnormalities included right ventricular dilatation and increased in left ventricular internal dimensions in 4 cases (7.8%), respectively. Thirteen cases (25.5%) had normal echocardiographic findings. Forty (78%) patients had sinus tachycardia while 8 cases (15.7%) showed atrial fibrillation with uncontrolled ventricular rate, and 3 (5.8%) had sinus bradycardia. Heat stroke electrocardiograms showed tracings demonstrating ST segment depression, compatible with ischaemia in 9 cases, while in 6 cases there were nonspecific T wave changes, whereas in another 4 cases the tracings demonstrated different conduction abnormalities. The collected data were analysed and compared to those of 43 control patients. The adverse effects of heat stroke on the heart are multifactorial requiring the utmost attention and understanding, as they reflect the patient's cardiovascular status.
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PMID:Non-invasive evaluation of cardiac abnormalities in heat stroke pilgrims. 145 70

The mother and three children of a family whose parents were consanguineous, each had cardiomyopathy with various patterns of hypertrophy and dilatation. All members had asymmetrical septal hypertrophy (ASH), and three of them were characterized as hypertrophic cardiomyopathy (HCM). Another one had ventricular dilatation mimicking dilated cardiomyopathy (DCM). Case 1: The 57-year-old mother had a typical ASH pattern; her septal/posterior wall thickness ratio (IVST/LVPWT) was 2.5. Case 2: The 37-year-old daughter had basal septal hypertrophy. Case 3: The 32-year-old elder son had typical concentric hypertrophy. Case 4: The 30-year-old younger son had an episode of congestive heart failure, and showed DCM-like features with considerable dilatation and impaired wall motion of the left ventricle. The hypertrophic pattern in cardiomyopathies is thought to depend partially on the ages of the onset, or its evolution with aging.
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PMID:[Familial cardiomyopathy with different clinical features in individual members]. 350 15

Serial obstetric ultrasound showed the development of asymmetrical ventricular dilatation between 28 and 32 weeks' gestation. After delivery at 38 weeks, progressive ventricular dilatation required a ventriculo-atrial shunt. Investigation of postoperative bleeding into the cerebral ventricles consistently showed factor V values of only two per cent.
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PMID:Factor V deficiency and antenatal intraventricular haemorrhage. 638 13

The mechanism for the development of functional tricuspid regurgitation (TR) was studied by an ultrasonic method. Thirty-five examinations were performed in 31 patients who were expected to have functional TR, and the severity was classified into 4 grades according to the extension of the regurgitant signals by pulsed Doppler echocardiography. The satisfactory horizontal section of the tricuspid valve was obtained by two-dimensional echocardiography (2DE) to measure the tricuspid annular diameter and to observe systolic configuration of the tricuspid valve in 22 examinations. The tricuspid annular diameter was well correlated with the severity of TR, and "lack of coaptation" of the valve was recognized on 2DE in some cases of severe TR with the markedly dilated annulus, indicating that this dilatation was an important trigger of functional TR. Additionally, in the majority of patients with severe TR, "anterior displacement" of the tips of tricuspid leaflet(s) (6 mm or more from the tricuspid annulus towards the right ventricle) was observed, which was thought to be due to the chordal traction secondary to the right ventricular dilatation, and contributed to the development of functional TR by disturbing sufficient coaptation. In one particular case, severe TR was associated with " malaligned coaptation" caused by the anterior displacement confined to the septal leaflet, indicating that asymmetrical dilatation of the right ventricle and/or disorientation of chordae-valve system may contribute to TR.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:[Functional tricuspid regurgitation and its relation to the morphology of the tricuspid valve and annulus: pulsed doppler echocardiography and two-dimensional echocardiography]. 667 71

Massive ventricular dilatation causes stretching and dehiscence of the fornix with formation of unilateral or bilateral pial pulsion diverticula of the inferior medial wall of the atrium. Enlargement of the pial pouch creates a dramatic subarachnoid cyst that may herniate downward through the incisura into the lateral mesencephalic, precentral cerebellar, and superior vermian cisterns where it displaces the brain stem, vermis, and fourth ventricle. Lateral ventricular diverticula may be identified and distinguished from the dilated fourth ventricle and dilated suprapineal recess, with which they are so commonly confused, when all of the following signs are apparent on computed tomography (CT): (1) marked unilateral or bilateral atrial dilatation; (2) focal dehiscence of the medial atrial wall; (3) ipsilateral shortening of the tentorial band in axial section; (4) focal defect in the tentorial band in coronal section; (5) draping of the medial atrial wall over the free margin of tentorium, with continuity of cerebrospinal fluid density around the edge of tentorium in axial and/or coronal sections; (6) bowing of the crus (or crura) of fornix; (7) separation of fornix from splenium, with visualization of the hernia ostium; (8) asymmetrical position of the choroid plexi, which attach to and define the lateral borders of the fornices; (9) contralateral displacement of the internal cerebral veins; and (10) septa separating diverticulum from third ventricle
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PMID:Atrial diverticula in severe hydrocephalus. 680 75

Ventriculitis developed suddenly in a patient with an undiagnosed abscess and was accompanied by obtundation, fever, meningismus, and hemiplegia. Aspiration of a streptococcal thalamic abscess and high doses of intravenous penicillin produced marked improvement. Increasing dysphasia 5 weeks later was accompanied by ventricular dilatation, most marked on the left, with no evidence of recurrent abscess. The left foramen of Monro was demonstrably patent. Shunting relieved the symptoms of aphasia; they recurred with one episode of malfunction of the shunt. This case lends support to the belief that parenchymal characteristics are important in hydrocephalus and demonstrates how asymmetrical ventricular dilatation can produce focal symptoms.
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PMID:Asymmetrical hydrocephalus following ventriculitis from rupture of a thalamic abscess. 685 81

When determining a management plan for infantile hydrocephalus, the determining factor for or against the implantation of a shunt is the degree of ventricular dilatation. The author has devised a standardised method of estimating this, the use of which has been shown to achieve consistently successful results. Dilatation was determined using the ventricular/biparietal (V/BP) ratio from the axial CT scan at the mid-portion of the bodies of the lateral ventricles, showing the greatest ventricular dilatation. According to this method, hydrocephalus was classified into four grades. These were mild (V/BP ratio 0.26-0.40), moderate (V/BP ratio 0.41-0.60), severe (V/BP ratio 0.61-0.90) and extreme (V/BP ratio 0.91-1). A V/BP ratio of less than 0.26 was considered normal. This method appeared to be accurate and reproducible in infants with hydrocephalus including those with asymmetrical and multiloculated ventricular dilatation. In all the patients with mild hydrocephalus, spontaneous regression or stabilisation occurred and their developmental outcome was normal. Patients with moderate and severe hydrocephalus needed a ventricular shunt and the developmental outcome was satisfactory in 87% of the cases. They were functionally normal although 18 had some abnormal neurological signs. In patients with extreme hydrocephalus the developmental outcome following shunting was satisfactory in 31% of the cases. They were functionally normal although four had abnormal neurological signs. This plan of management was used in a total of 144 infants and it proved to be highly successful.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Infantile hydrocephalus: management using CT assessment. 762 83

We investigated the hydrocephalus in 24 patients associated with acoustic neurinoma. We found the high incidence of homo-lateral ventricular dilatation to the side of the acoustic neurinoma. Utilizing magnetic resonance imaging, the diameter of the tumor parallel to the pyramidal bone, diameter of the tumor perpendicular to the pyramidal bone, grade of the 4th ventricle deviation, and the shape of the tumor (round or oval) were analyzed. Ten (42%) of the 24 patients with acoustic neurinoma were found to have hydrocephalus. Seven (70%) of the 10 patients with hydrocephalus exhibited asymmetrical lateral ventricle dilatation: in all cases the lateral ventricle in the hemisphere homolateral to the acoustic neurinoma was larger than that of the contralateral side. The hydrocephalus was not related to the grade of the 4th ventricle deviation but rather to the diameter of the tumor parallel to the pyramidal bone (p < 0.01). The diameter of the tumor parallel to the pyramidal bone was also related to the asymmetrical lateral ventricular dilatation (p < 0.05).
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PMID:MRI analysis of hydrocephalus associated with acoustic neurinoma. 1475 4


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