1.A Case of Clear Cell Sarcoma of the Anterior Chest.
Sang Hak LEE ; Jin Ho CHO ; Seung Min HONG ; Byung Mun CHOI ; Yoo Shin LEE
Korean Journal of Dermatology 1989;27(4):477-480
Clear cell sarcoma of tendon and aponeurosis is a rare malignant tumor. It occurs chiefly in young adults, predominates in women and is most common in the regions of the foot and ankle. We report a case of clear cell sarcoma of tendon and aponeurosis in s 22-year-old man. he pstient had had a asymptomatic, normal skin colored, relativerly hard, dome shsped nodule on the anterior chest for 6 months. Histopsthologic findings revealed uniform pattern composed of compact nests of round or fusiform cells which had clear cytoplasm and were surrounded by delicate framework of fibrocollagenous tissue, and the individual tumor cell had a fairly regular appearance of possessing round to avoid vesicular nucleus with prominent basophilic nucleolus. One year after surgical excision and post operative radiotherapy, there was no recurrence.
Ankle
;
Basophils
;
Cytoplasm
;
Female
;
Foot
;
Humans
;
Radiotherapy
;
Recurrence
;
Sarcoma, Clear Cell*
;
Skin
;
Tendons
;
Thorax*
;
Young Adult
2.Nontraumatic Spinal Epidural Hematoma - An Analysis of The Etiology -.
Dae Young HONG ; Mun Chul KIM ; Sang Pyung LEE ; Gi Hwan CHOI ; Hyung Tae YEO
Journal of Korean Neurosurgical Society 2002;31(1):89-94
Spontaneous spinal epidural hematoma is a rare entity. Various definitions for spontaneous epidural hematoma have been reported in the literature. The expression of nontraumatic spinal epidural hematoma seems to be less ambiguous and includes idiopathic hematomas and hematomas secondary to coagulopathy, vascular malformations, and tumors. We report three cases of nontraumatic spinal epidural hematomas observed from 1991 to 2000. The causes of the spinal epidural hematomas were not clear in two cases among them, but in the another one case, the cause was determined to be an acquired coagulopathy. We reviewed 24 cases reported in the Korean Journal of Neurosurgery and our three cases with particular emphasis on the various causes such as coagulopathy, vascular malformations and tumors. Among the 27 cases, numerous causes were detected such as three cases of vascular malformation, one case of anticoagulant treatment, five cases of combined lumbar disc herniation, two cases associated with pregnancy and postpartum, one case associated with hypertension, and one case associated with ossification of ligamentum flavum. No causes were detected in the ten cases. The authors reviewed the literature.
Hematoma
;
Hematoma, Epidural, Spinal*
;
Hypertension
;
Ligamentum Flavum
;
Neurosurgery
;
Postpartum Period
;
Pregnancy
;
Vascular Malformations
3.Clinical study on intranasal injection of steroid in allergicrhinitis.
Ho Joon LEE ; Heon Sang SHIN ; Gyu Dong CHOI ; Gun Young MUN ; Chul Ho CHANG
Journal of the Korean Academy of Family Medicine 1991;12(2):28-31
No abstract available.
4.Primary Osteosarcoma of the Sphenoid Bone: Case Report.
Geun Jin YANG ; Mun Chul KIM ; Hoon CHUNG ; Sang Pyung LEE ; Gi Hwan CHOI ; Hyung Tae YEO
Journal of Korean Neurosurgical Society 2000;29(5):680-683
No abstract available.
Osteosarcoma*
;
Sphenoid Bone*
5.Clinical Roles of Continuous Lumbar Drainage in Acute Hydrocephalus Patients.
Geun Jin YANG ; Mun Chul KIM ; Hoon CHUNG ; Sang Pyung LEE ; Gi Whan CHOI ; Hyung Tae YEO
Journal of Korean Neurosurgical Society 2000;29(5):644-649
No abstract available.
Drainage*
;
Humans
;
Hydrocephalus*
6.A Study of Pattern Reversal Visual Evoked Potential and Flash Electroretinogram in Patients with Optic Atrophy.
Seong Uk HONG ; Dong Hun KIM ; Mun Sung CHOI ; Kyu Hyun PARK ; Sang Wook KIM
Journal of the Korean Neurological Association 1989;7(1):35-41
The pattern reversal visual evoked potential(PRVEP) and flash electroretinogram(flash ERG) were performed in 22 patients with optic atrophy. Patients with ophthalmologic problems other than optic atrophy or with systemic disorders were excluded from the analysis The results are as follows: 1. In the 41 eyes of patients with optic atrophy, 39 of them showed abnormal PRVEP, in which all the eyes had no consistent waveform except in one patient 2 eyes with delayed P1 latency. 2. 13 eyes were abnormal in both PRVEP and flash ERG but no eye was abnomnal in flash ERG only 3, Regarding the flash ERG examination, 13 eyes were abnomlal. Of these, there was a period of 1 to 2 years for 1 eye's disease, a period of 2 to 5 years for another eye' disease and after 5 years 11 eyes were diseased. Therefore, it showed that the longer the duration of disease lasted, the more flash ERG abnormalities developed. 4. The abnormalities of PRVEP haxe no significant relationship with the duration of the disease.
Evoked Potentials, Visual*
;
Humans
;
Optic Atrophy*
7.Study on Characteristics of Maxillofacial Growth in Class III Malocclusion Patients by Cranial Base Growth
Do Kyoung SON ; Sung Won PARK ; Jae Min LEE ; Eun Ja KIM ; Sang Mun CHOI ; Young Woon KIM ; Mun Gi CHOI ; Sung Hwan OH
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons 2011;33(6):483-489
8.A Case of Hereditary Progressive Dystonia With Diurnal Fluctuation.
Dong Hun KIM ; Sang Ok RA ; Seon Chool HWANG ; Mun Sung CHOI ; Kyu Hyun PARK ; Sang Wook KIM ; Dae Soo JUNG
Journal of the Korean Neurological Association 1990;8(2):344-348
Hereditary progressive dystonia develope in the first decade of ?life and is characterized by marked diurnal fluctuation of symptoms(dystonic postures and movements), i.e.symptoms aggrevated towards evening and alleviated after sleep. These symptoms and signs responded dramatically to levodopa. With the high incidence of familial cases this disorder is considers to be hereditary, but inheritance is not clear yet. Segawa regarded this disorder as a dystonia different from Parkinson's disease and other types of dystonic movement disorders, thereafter it has been reported under name of hereditary progressive dystonia with marked diurnal fluctuation.
Dystonia*
;
Incidence
;
Levodopa
;
Movement Disorders
;
Parkinson Disease
;
Posture
;
Wills
9.Agenesis of Right Internal Carotid Artery Associated with Intracranial Aneurysm: Case Report.
Sang Hoon SEOK ; Mun Chul KIM ; Sang Pyung LEE ; Gi Hwan CHOI ; Hyung Tae YEO
Journal of Korean Neurosurgical Society 2002;31(3):278-281
The authors present a case of unilateral agenesis of internal carotid artery associated with an aneurysm at the unusual site. A 22-years old female was admitted with sudden headache and nausea. She was alert on admission and no focal neurologic deficit was detected. Brain computed tomography(CT) scan showed subarachnoid hemorrhage. In the cerebral angiography, right internal carotid artery was absent and an aneurysm was arisen from the junction of the right middle cerebral artery and posterior communicating artery. The blood supply of the right anterior cerebral artery was maintained from the left internal carotid artery via the anterior commuicating artery. The territory of the right middle cerebral artery was supplied from the basilar artery through enlarged right posterior communicating artery. Direct clipping of the aneurismal neck was performed through right pterional approach. In the postoperative high resolution CT scan, there was no carotid canal in the right skull base suggesting agenesis of the right internal carotid artery.
Aneurysm
;
Anterior Cerebral Artery
;
Arteries
;
Basilar Artery
;
Brain
;
Carotid Artery, Internal*
;
Cerebral Angiography
;
Female
;
Headache
;
Humans
;
Intracranial Aneurysm*
;
Middle Cerebral Artery
;
Nausea
;
Neck
;
Neurologic Manifestations
;
Skull Base
;
Subarachnoid Hemorrhage
;
Tomography, X-Ray Computed
;
Young Adult
10.Gram-negative Bacillary Meningitis: A Case Report of E. coli Meningitis in Adult.
Seon Chool HWANG ; Sang Ok RA ; Geo Hyoung KIM ; Mun Seung CHOI ; Kyu Hyun PARK ; Sang Wook KIM
Journal of the Korean Neurological Association 1992;10(1):103-108
We treated a 66 year-old-male patient with non-traumatic spontaneous E. coli meningitis, whose cerebrospinal fluid showed turbid, and from which E. coli was cultured, and who had urinary tract infection and fatty liver disease which were thought to be predisposing factors to the meningitis. Gram-negative bacillary meningitis is a very rare condition after the neonatal period, and may be complicated by penetrating cranial injuries, neurosurgical interventions or such debilitating diseases as diabetes, liver cirrhosis, urinary tract infection, malignancy and alcholism, etc. It has a high mortality rate in spite of using various antibiotics.
Adult*
;
Anti-Bacterial Agents
;
Causality
;
Cerebrospinal Fluid
;
Fatty Liver
;
Humans
;
Liver Cirrhosis
;
Meningitis*
;
Mortality
;
Urinary Tract Infections