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1.
Korean Journal of Nephrology ; : 173-177, 1997.
Article in Korean | WPRIM | ID: wpr-188083

ABSTRACT

Spontaneous hemorrhage in the patients undergoing hemodialysis is the ralatively common problem, but spontaneous mediastinal hemorrhage in such patients reported only few cases. We experienced a case of spontaneous mediastinal hemorrhage in chronic hemodialysis patient who complained of continuous pleuritic chest pain and mild dyspnea. The diagnosis was made dy chest computed tomography,magnetic resonance imaging and percutaneous fine needle aspiration of liquified dark reddish old blood material guided by ultrasonography. Treatment is usually conservative, with blood volume replacement and intensive hemodialysis using regional heparinization. We report on a patient undergoing hemodialysis due to endstage renal disease who developed spontaneous mediastinal hemorrhage.


Subject(s)
Humans , Biopsy, Fine-Needle , Blood Volume , Chest Pain , Diagnosis , Dyspnea , Hemorrhage , Heparin , Renal Dialysis , Thorax , Ultrasonography
2.
Journal of the Korean Pediatric Society ; : 854-860, 1994.
Article in Korean | WPRIM | ID: wpr-212365

ABSTRACT

A synophthalmia, another form of cyclopia, in which the element of the two eyes are partially fused to form an apparently single eye in the middle of the forehead. The synophthalmia is a result of complex, neural plate misdevelopment syndrome involving the eye, brain, skull and face. It is well known that synophthalmia is due to heterogenous causes, most of which chromosomal imbalances. We experienced a case of synophthalmia associated with proboscis, alobar holoprosencephaly and chromosomal anomaly 46, XX, -15,t (15 q, 21 q). Diagnosis was confirmed by brain MRI and autopsy, The patient died about 20 hours of age and autopsy was done. A brief review of the literatures was also presented.


Subject(s)
Humans , Autopsy , Brain , Diagnosis , Forehead , Holoprosencephaly , Magnetic Resonance Imaging , Neural Plate , Skull
3.
Journal of the Korean Pediatric Society ; : 877-881, 1993.
Article in Korean | WPRIM | ID: wpr-162600

ABSTRACT

The unilateral megalencephaly is a rare brain malformation characterized by cerebral asymmetry and cortical dysplasia caused by faulty migration of the subependymal neuroblasts. We experienced a case of unilateral megalencephaly in a two day-old male with the chief complaint of asymmetric head appearance. Large left hemisphere with agyria, pachygyria, dilatation of lateral ventricle, and the thick cortex of the ipsilateral hemisphere were showed in brain MRL, Clinical findings in this case were intractable seizure, hemiparesis, and psychomotor retardation. A review of literatures was also presented briefly.


Subject(s)
Humans , Male , Brain , Dilatation , Head , Lateral Ventricles , Lissencephaly , Malformations of Cortical Development , Paresis , Seizures
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