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1.
Singapore medical journal ; : e204-7, 2012.
Article Dans Anglais | WPRIM | ID: wpr-249633

Résumé

Epithelioid angiomyolipoma is a recently described rare variant of renal angiomyolipoma. It can occur in patients with or without tuberous sclerosis. We report the imaging findings of a case of epithelioid angiomyolipoma that showed the presence of fatty tissue undifferentiated from the typical angiomyolipoma at the beginning. After partial nephrectomy, tumour recurrence occurred two years later, presenting as completely solid tumours with no adipose tissue, and with invasion into the psoas muscle and left adrenal gland. Differentiation of this tumour from renal cell carcinoma is difficult. Both the radiologist and surgeon should be aware of the existence of this tumour and its potentially malignant behaviour.


Sujets)
Sujet âgé , Femelle , Humains , Angiomyolipome , Diagnostic , Anatomopathologie , Chirurgie générale , Néphrocarcinome , Diagnostic , Diagnostic différentiel , Rein , Anatomopathologie , Tumeurs du rein , Diagnostic , Anatomopathologie , Chirurgie générale , Récidive tumorale locale , Anatomopathologie , Tomodensitométrie
2.
Korean Journal of Radiology ; : 481-489, 2009.
Article Dans Anglais | WPRIM | ID: wpr-72775

Résumé

OBJECTIVE: This study was designed to determine if existing methods of grading liver function that have been developed in non-Asian patients with cirrhosis can be used to predict mortality in Asian patients treated for refractory variceal hemorrhage by the use of the transjugular intrahepatic portosystemic shunt (TIPS) procedure. MATERIALS AND METHODS: Data for 107 consecutive patients who underwent an emergency TIPS procedure were retrospectively analyzed. Acute physiology and chronic health evaluation (APACHE II), Child-Pugh and model for end-stage liver disease (MELD) scores were calculated. Survival analyses were performed to evaluate the ability of the various models to predict 30-day, 60-day and 360-day mortality. The ability of stratified APACHE II, Child-Pugh, and MELD scores to predict survival was assessed by the use of Kaplan-Meier analysis with the log-rank test. RESULTS: No patient died during the TIPS procedure, but 82 patients died during the follow-up period. Thirty patients died within 30 days after the TIPS procedure; 37 patients died within 60 days and 53 patients died within 360 days. Univariate analysis indicated that hepatorenal syndrome, use of inotropic agents and mechanical ventilation were associated with elevated 30-day mortality (p 11 or an MELD score > 20 predicted increased risk of death at 30, 60 and 360 days (p 11 or an MELD score > 20 are predictive of mortality in Asian patients with refractory variceal hemorrhage treated with the TIPS procedure. An APACHE II score is not predictive of early mortality in this patient population.


Sujets)
Femelle , Humains , Mâle , Adulte d'âge moyen , Traitement d'urgence , Varices oesophagiennes et gastriques/mortalité , Anastomose portosystémique intrahépatique par voie transjugulaire/mortalité , Valeur prédictive des tests , Pronostic , Modèles des risques proportionnels , Courbe ROC , Études rétrospectives , Analyse de survie
3.
Korean Journal of Radiology ; : 390-390, 2008.
Article Dans Anglais | WPRIM | ID: wpr-215031

Résumé

In previous case report entitled "Multidetector CT findings of a congenital coronary sinus anomaly: a report of two cases" by Chou et al. (Korean J Radiol 2008;9:S1-S6), there were mistakes. "The Figure 1A and 1B are the MDCT findings of normal coronary sinus of a normal individual." "The Figure 1C to 1E are the MDCT findings of congenital coronary sinus anomaly in 60-year-old woman with Ebstein's anomaly." "The Figure 2J and 2K are illustration of atresia of the right atrial ostium of the coronary sinus with/without PLSVC"

4.
Korean Journal of Radiology ; : S1-S6, 2008.
Article Dans Anglais | WPRIM | ID: wpr-65672

Résumé

Congenital coronary sinus anomalies are extremely rare, and they have received relatively little attention. This is probably due to the lack of both clinical symptoms and significant cardiac functional disturbance. We present two cases of a coronary sinus anomaly and briefly review the literature. Recognizing and being familiar with the variations of a congenital coronary sinus anomaly in congenital heart disease may avoid a misinterpretation of cardiac catheterization findings and the troublesome disruption of coronary sinus blood return during the surgical management of cardiac lesions.


Sujets)
Femelle , Humains , Adulte d'âge moyen , Sinus coronaire/malformations , Tomodensitométrie
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