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A Case of Insulinoma Diagnosed as Epilepsy for 7 Years / 대한내분비학회지
Journal of Korean Society of Endocrinology ; : 265-271, 1994.
Article in Korean | WPRIM | ID: wpr-765469
ABSTRACT
Insulinoma is rare functioning islet cell tumor of pancreas and its main feature is frequent attacks of hypoglycemia. Because of frequent seizure, the disease is occasionally mistook as epilepy. We experienced a case of insulinoma with dilantin toxicity in a 45 year old patient who had been treated with dilantin for 7 years. Selective splenic arteriogram showed 0.8cm mass in the tail of pancreas which was proven insulin secreting tumor on histiopathological examination. After operation no more seizure attack was detected and her blood sugar level was well maintained within normal range. This case might provide an insight that the possibility of insulinoma should be considered in patient with episodic neurobehavioral dysfunction such as epilepsy.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pancreas / Phenytoin / Reference Values / Seizures / Tail / Blood Glucose / Adenoma, Islet Cell / Epilepsy / Hypoglycemia / Insulin Type of study: Diagnostic study Limits: Humans Language: Korean Journal: Journal of Korean Society of Endocrinology Year: 1994 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pancreas / Phenytoin / Reference Values / Seizures / Tail / Blood Glucose / Adenoma, Islet Cell / Epilepsy / Hypoglycemia / Insulin Type of study: Diagnostic study Limits: Humans Language: Korean Journal: Journal of Korean Society of Endocrinology Year: 1994 Type: Article