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1.
Journal of Korean Diabetes ; : 98-101, 2013.
Artigo em Coreano | WPRIM | ID: wpr-726959

RESUMO

A 47-year-old male with recurrent abnormal behavior for ten years was referred to our clinic. He was diagnosed with insulinoma and cognitive dysfunction. Persistent hypoglycemia leads to a high risk of cognitive dysfunction in diabetic patients. However, cognitive dysfunction associated with insulinoma is rare. In this case study, cognitive dysfunction was confirmed by neurological testing.


Assuntos
Humanos , Masculino , Hipoglicemia , Insulinoma
2.
Journal of Korean Medical Science ; : 489-492, 2013.
Artigo em Inglês | WPRIM | ID: wpr-33017

RESUMO

In patients with primary aldosteronism who have bilateral adrenal incidentalomas, it is important to identify which adrenal gland is secreting excess aldosterone. Traditionally, adrenal vein sampling (AVS) has been performed for lateralization despite its invasiveness. Here we report a case of bilateral adrenal incidentaloma in which 18-Fluorodeoxyglucose (FDG)-positron emission tomography (PET) was used to identify the functional adrenal mass. A 53-yr-old man was referred to our clinic due to bilateral adrenal incidentalomas (right: 1 cm, left: 2.5 cm) on computed tomography (CT). Given his history of colon cancer, FDG-PET/CT scanning was used to rule out metastasis. Although there was focal hot uptake lesion in the right adrenal gland, the patient was suspected primary aldosteronism clinically more than metastasis because of the patient's underlying hypertension with hypokalemia. It was consistent with the results of AVS. Based on these findings, we propose that FDG-PET/CT can be used instead of AVS to identify the source of primary aldosteronism between two bilateral adrenal incidentalomas.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias das Glândulas Suprarrenais/diagnóstico , Glândulas Suprarrenais/patologia , Fluordesoxiglucose F18 , Hiperaldosteronismo/diagnóstico , Hipertensão/diagnóstico , Hipopotassemia/diagnóstico , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada
3.
Korean Journal of Obstetrics and Gynecology ; : 1991-1995, 2004.
Artigo em Coreano | WPRIM | ID: wpr-55325

RESUMO

The HELLP syndrome, which is characterized by hemolysis, elevated liver enzymes and low platelets, complicates 4 to 14% of preeclamptic or eclamptic pregnancy. Its course is usually benign except when spontaneous hepatic rupture, a rare catastrophic event, threatens life. The authors have experienced one case of spontaneous hepatic rupture in HELLP syndrome during immediate postpartum period, which was treated with surgical intervention on the first postpartum day. We report this case with a brief review of the literatures.


Assuntos
Feminino , Gravidez , Síndrome HELLP , Hemólise , Hemorragia , Fígado , Período Pós-Parto , Ruptura
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