1.A Case of Vigabatrin Induced Symptomatic Visual Field Defect.
Keun Yong UM ; Sung Min KIM ; Byung Ju LEE ; Hong Ki SONG ; Ki Han KWON ; Byung Chul LEE ; Jin Soek OH ; Kyung Hwa LEE
Journal of the Korean Neurological Association 2000;18(2):232-234
Vigabatrin (VGB) is one of the most frequently prescribed new anti-epileptic drugs in the world since 1989. It has minimal side effects and fewer drug interactions with other anti-epileptic drugs. Recently, concern of the prevalence and pathophysiology of visual impairment with VGB has been increased since the reports of visual field constriction in patients treated with VGB. We report a 46-year-old man with a visual field defect who has been suffering from complex partial seizures for 29 years. Brain magnetic resonance image (MRI) and electroencephalogram (EEG) were non-specific. The frequency of seizures was about 5 times a month for the past 5 years. VGB, in a dose of 1500 mg/day, was prescribed as an add on drug in addition to carbamazepine. 19 months after VGB treatment, the patient complained of visual dimness especially in the lower half of the visual field. He expressed it as "waving". He had no metabolic derangement. Fundus examination, visual evoked potential, and electroretinogram showed normal findings. A visual field analysis showed a bilateral field defect in the lower half. A follow up visual field analysis, 6 months after the withdrawal of VGB, revealed a slight improvement of visual field defects which were noted without significant clinical improvement. This case implicates that visual field defects due to VGB may be partially reversible.
Brain
;
Carbamazepine
;
Constriction
;
Drug Interactions
;
Electroencephalography
;
Evoked Potentials, Visual
;
Follow-Up Studies
;
Humans
;
Middle Aged
;
Prevalence
;
Seizures
;
Vigabatrin*
;
Vision Disorders
;
Visual Fields*
2.A Case of Splenic Artery Aneurysm Rupture.
Dong Wun SHIN ; Ah Jin KIM ; Jun Soek PARK ; Kyung Hwan KIM ; Kyung Ah KIM ; Dong Hoon OH ; Yoon Hee HAN ; Young Gil KO
Journal of the Korean Society of Emergency Medicine 2006;17(1):92-94
Splenic artery aneurysms are an uncommon form of vascular disease that carry the risk of rupture and fatal hemorrhage. Precise cause of splenic artery aneurysms are not be established, the most common pathologic finding is defect of the media. Splenic artery aneurysms occur in patient with multiple pregnancies, portal hypertension, splenomegaly, after orthotopic liver transplantation and fibrodysplasia. Most patients who are diagnosised with splenic artery aneurysm are asymptomatic. Arteriography is a confirmed diagnostic method for detecting splenic artery aneurysms and searching the location of aneurysms. Operative treatment and therapeutic catheter embolization have been used for treatment of splenic artery aneurysms.
Aneurysm*
;
Angiography
;
Catheters
;
Diagnosis
;
Embolization, Therapeutic
;
Female
;
Hemorrhage
;
Humans
;
Hypertension, Portal
;
Liver Transplantation
;
Pregnancy
;
Pregnancy, Multiple
;
Rupture*
;
Splenic Artery*
;
Splenomegaly
;
Vascular Diseases
3.A Hepatic Lymphoma Mimicking Multiple Liver Metastases or an Intrahepatic Cholangiocarcinoma.
Joo Hyun OH ; Mun Seok CHOI ; Dong Hyeon SHIN ; Soek Jin KIM ; Tae Uk KANG ; Yeong Hye KOH
Korean Journal of Medicine 2018;93(3):285-290
A primary hepatic lymphoma (PHL) is a rare malignancy; misdiagnosis and mistreatment are very common. We report the case of a 56-year-old female who presented with a 2-week history of upper abdominal pain. She exhibited no risk factors for hepatocellular carcinoma (HCC) and her serum tumor marker levels were normal. A computed tomography scan and gadolinium-enhanced magnetic resonance imaging of the liver revealed multiple liver masses, suggestive of multiple liver and lung metastases or an intrahepatic cholangiocarcinoma with lung metastasis. A diagnosis of PHL (a diffuse large B cell lymphoma) was confirmed by biopsy followed by immunohistochemistry. This case emphasizes that a PHL must be considered in the differential diagnosis of space-occupying liver lesions in patients with no risk factors for HCC and normal levels of serum tumor markers. It is notable that neither B cell lymphoma symptoms nor an elevated lactate dehydrogenase level were apparent in this case. We thus report a case of PHL mimicking multiple liver metastases or an intrahepatic cholangiocarcinoma, and we review the literature.
Abdominal Pain
;
Biomarkers, Tumor
;
Biopsy
;
Carcinoma, Hepatocellular
;
Cholangiocarcinoma*
;
Diagnosis
;
Diagnosis, Differential
;
Diagnostic Errors
;
Female
;
Humans
;
Immunohistochemistry
;
L-Lactate Dehydrogenase
;
Liver Neoplasms
;
Liver*
;
Lung
;
Lymphoma*
;
Lymphoma, B-Cell
;
Lymphoma, Large B-Cell, Diffuse
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Lymphoma, Non-Hodgkin
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Magnetic Resonance Imaging
;
Middle Aged
;
Neoplasm Metastasis*
;
Risk Factors