1.A Case of Trichoblastic Fibroma.
Hwa Jung LEE ; Dong Jin IM ; Ho Seok SUH ; Jee Ho CHOI ; Jai Kyoung KOH
Annals of Dermatology 1996;8(4):265-268
Trichogenic tumors are very rare and described as cutaneous neoplasms probably derived from hair germ which develops into hair follicles. We report a case of trichoblastic fibroma on the left parietal scalp of a 45-year-old man. The lesion was a solitary, firm, non-tender, 2×2cm subcutaneous nodule. The histopathological study showed a well circumscribed dermal tumor composed of abundant basophilic palisading basaloid lobules with some keratinous cysts, hair follicle differentiation and fibroblastic stroma.
Basophils
;
Fibroblasts
;
Fibroma*
;
Hair
;
Hair Follicle
;
Humans
;
Middle Aged
;
Rabeprazole
;
Scalp
2.A clinical effect of retreatment by prothionamide, cycloserine, para-aminosalicylic acid, streptomycin(kanamycin or tuberactinomyc-in) on pulmonary tuberculosis.
Cheol Shick SHIN ; Young Jae IM ; Young Jun KIM ; Seok Shin KOH ; Moon Shik KIM
Tuberculosis and Respiratory Diseases 1992;39(2):167-171
No abstract available.
Aminosalicylic Acid*
;
Cycloserine*
;
Prothionamide*
;
Retreatment*
;
Tuberculosis, Pulmonary*
3.Children with Centrotemporal Spikes: Clinical and EEG Characteristics.
Journal of Korean Epilepsy Society 2001;5(1):18-21
BACKGROUND: Centrotemporal spikes (CTS) are the hallmark of the syndrome of benign childhood epilepsy with centrotemporal spikes or Rolandic seizures. However, they also can be encountered in other symptomatic epilepsies or may incidentally be found in non-epileptic children with or without neurological symptoms. We investigated clinical and electroencephalographic characteristics of children with CTS on EEG. METHODS: A 7 year material of children with CTS on EEG were reviewed. Sixty-eight children were found. RESULTS: Among them, 55 patients exhibited recurrent rolandic seizures of benign course (so-called benign rolandic epilepsy ; BRE), 9 children suffered from chronic headache without clinical seizure, three patients showed multiple types of seizures or rolandic seizures with some degree of mental retardation, and one child was asymptomatic. In 55 BRE cases, seven children (13%) had a preceding history of febrile convulsions, and a positive family history of epilepsy was found in 9 patients. Generalized spike and wave discharges were observed in 9 patients (16.7%), but none of them experienced clinical absence seizure. In 25 of 29 BRE patients who showed overt lateralized ictal manifestations on history, symptoms were correlated with the main foci of spike discharges. Of the nine children, found to have CTS during evaluation of chronic intermittent or daily headache, the headache was successfully controlled by antiepileptic drugs in two cases. CONCLUSION: Most children with CTS were compatible to the BRE without any causative lesional factor. However, nonepileptic cases were not uncommon and, though rare, atypical cases were also present in children with CTS on EEG.
Anticonvulsants
;
Child*
;
Electroencephalography*
;
Epilepsy
;
Epilepsy, Absence
;
Epilepsy, Rolandic
;
Headache
;
Headache Disorders
;
Humans
;
Intellectual Disability
;
Seizures
;
Seizures, Febrile
4.Left to right ratio of autopneumonectomy state in pulmonary tubercu-losis patients.
Cheol Shick SHIN ; Jae Man JEONG ; Young Jae IM ; Young Jun KIM ; Seok Shin KOH ; Moon Shik KIM
Tuberculosis and Respiratory Diseases 1992;39(4):343-347
No abstract available.
Humans
5.Transient mesial temporal abnormalities associated with partial seizures of temporal lobe origin.
Hong Ki SONG ; Hyoung Cheol KIM ; Im Seok KOH ; Woon San KOH ; Byung Chul LEE
Journal of the Korean Neurological Association 1997;15(3):660-664
Seizure induced transient brain CT or MRI abnormalities following status epilepticus have previously been reported. However, focal transient imaging abnormalities involving hippocampus or mesial temporal lobe as a consequence of seizure are rare findings. We report 2 patients with transient mesial temporal abnormalities on MRI associated with partial seizure of temporal lobe origin. A 59-year-old man with a 4-month history of occasional epigastric rising sensation had developed frequent olfactory hallucination 7 days prior to presentation. On brain MRI, T2 signal was increased in the right mesial temporal region, and the lesion showed mild mass effects and partial enhancement after gadolinium injection. Interictal spikes were noted from right nasopharyngeal electrode, but there was no clinical or electrical evidence of status epilepticus during prolonged scalp/sphenoidal EEG monitoring. His seizures were successfully controlled by phenytoin. T2 high signal was markedly decreased and prior enhancement was no longer seen on brain MRI done 5 weeks later. A 33-year old woman with a 6 month history of occasional vacant staring and oral automatism with amnesia complained progressive memory impairment. Right amygdala and hippocampal head was enlarged and showed T2 high signal without contrast enhancement. EEG with sphenoidal electrodes showed right sphenoidal spikes. Her seizures were controlled by carbamazepine and brain MRI became unremarkable 6 weeks later. Suggested mechanisms and significance of the transient imaging abnormalities following seizures will be briefly reviewed.
Adult
;
Amnesia
;
Amygdala
;
Automatism
;
Brain
;
Carbamazepine
;
Electrodes
;
Electroencephalography
;
Female
;
Gadolinium
;
Hallucinations
;
Head
;
Hippocampus
;
Humans
;
Magnetic Resonance Imaging
;
Memory
;
Middle Aged
;
Phenytoin
;
Seizures*
;
Sensation
;
Status Epilepticus
;
Temporal Lobe*
6.Hypertensive Brainstem Encephalopathy in a Patient with Acute Lacunar Infarction.
In Gun HWANG ; Min Gu KIM ; Im Seok KOH ; Jong Yun LEE ; Sook Young ROH
Journal of the Korean Neurological Association 2017;35(2):114-116
No abstract available.
Brain Diseases*
;
Brain Stem*
;
Humans
;
Hypertensive Encephalopathy
;
Stroke, Lacunar*
7.Improvement of Bilateral Parkinsonian Symptoms After Unilateral Intracerebral Hemorrhage.
Hyo Eun LEE ; Yong Uk KWON ; Hye Young PARK ; Phil Za CHO ; Im Seok KOH ; Jong Yun LEE
Journal of the Korean Neurological Association 2010;28(2):125-126
No abstract available.
Cerebral Hemorrhage
;
Parkinson Disease
8.Microalbuminuria in non-diabetic patients with cerebral infacrtion.
Hyung Chul KIM ; Woon San KO ; Im Seok KOH ; Hong Ki SONG ; Byung Chul LEE
Journal of the Korean Neurological Association 1999;17(2):206-210
BACKGROUND: Microalbuminuria predicts cardiovascular events in diabetic and non-diabetic patients. But, few studies have addressed the relationship between microalbuminuria and cerebral infarction. We determined the incidence of microalbuminuria in non-diabetic subjects with cerebral infarction and investigated the relationship between urinary albumin excretion and risk factors of the stroke. METHODS: Urinary albumin excretion rate, 24 hours blood pressure monitoring, fasting serum lipid profiles, fibrinogen, fasting glucose, insulin and c-peptide were evaluated in 50 non-diabetic patients with acute cerebral infarction and matched 48 controls. RESULTS: Microalbuminuria was detected in 23 of 50(46%) patients with acute cerebral infarction and 4 of 48(8%) control subjects. Hypertension was present in 13 of 23(57%) microalbuminuric patients and 9 of 27(33%) non-microalbuminuric patients. In the microalbuminuric patients with cerebral infarction, diastolic blood pressure and fasting glucose were significantly greater than the control group. But, no difference in systolic blood pressure, lipid level, fibrinogen, fasting insulin and c-peptide level. CONCLUSIONS: The prevalence of microalbuminuria in patients with cerebral infarction was higher than controls and it was associated with increased diastolic blood pressure(DBP) and fasting blood glucose(FBS). Therefore, microalbuminuria is associated with thrombogenic cerebral infarction and it was partly mediated by DBP and FBS.
Blood Pressure
;
Blood Pressure Monitors
;
C-Peptide
;
Cerebral Infarction
;
Fasting
;
Fibrinogen
;
Glucose
;
Humans
;
Hypertension
;
Incidence
;
Insulin
;
Prevalence
;
Risk Factors
;
Stroke
9.A Case of Adrenomyeloneuropathy Confirmed by Serum Very Long Chain Fatty Acids Level.
Heue Jung PARK ; Im Seok KOH ; Sang Hyeon LEE ; Heue Kyung KWON ; Phil Za CHO ; Il Nam SUNWOO
Journal of the Korean Neurological Association 2001;19(4):427-430
A 31-year-old male patient was admitted to the department of neurology for progressive spastic paraparesis and sen-sory deficit in bilateral lower legs. On review of system, he had decreased libido and mild urinary frequency. On neuro-logic examination, he showed paraparesis, lower limb hypesthesia, bilateral hyperactive knee jerk and bilateral positive Babinski sign. The nerve conduction studies were sensori-motor demyelinating polyneuropathy. For spastic paraparesis and peripheral neuropathy, we approached adrenomyeloneuropathy and ascertained elevated serum very long chain fatty acids (VLCFA) level. (J Korean Neurol Assoc 19(4):427~430, 2001)
Adrenoleukodystrophy*
;
Adult
;
Fatty Acids*
;
Humans
;
Hypesthesia
;
Knee
;
Leg
;
Libido
;
Lower Extremity
;
Male
;
Neural Conduction
;
Neurology
;
Paraparesis
;
Paraparesis, Spastic
;
Peripheral Nervous System Diseases
;
Polyneuropathies
;
Reflex, Babinski
10.Neurosarcoidosis after Uveitis.
Jae Wook CHO ; Jin Woo JUNG ; Yeon Kyung JUNG ; Im Seok KOH ; Hyun Kyung KIM ; Jong Yun LEE
Journal of the Korean Neurological Association 2014;32(4):337-338
No abstract available.
Cranial Nerve Diseases
;
Uveitis*