1.A survey of deaths in hospitalized patients for pulmonary tuberculosis.
Seung Joon OH ; Ki Heon YOON ; Jee Hong YOO ; Hong Mo KANG
Tuberculosis and Respiratory Diseases 1993;40(6):694-699
No abstract available.
Humans
;
Tuberculosis, Pulmonary*
2.Clinical analysis on sudden sensorineural hearing loss.
Bo Sung JANG ; Sung Lee SHIN ; Seung Mo HONG ; Hee Young YOON ; Eun Chang CHOI
Korean Journal of Otolaryngology - Head and Neck Surgery 1991;34(5):913-920
No abstract available.
Hearing Loss, Sensorineural*
3.Three Cases of Mobius Syndrome in a Family
Hwan Mo JEONG ; Seung Hee HONG ; Dong Jin SHIN
Journal of the Korean Neurological Association 1996;14(4):1035-1041
Mobius syndrome is generally considered to be a static disorder of congenital origin, and is manifested as unilateral or bilateral facial weakness and lateral gaze limitation. In most instances the syndrome occurs sporadically, but rarely familial cases have been reported. We report a family of three members with Mobius syndrome; a 7-year-old girl, a 6-year-old boy, and their 29-year-old mother. Each patient revealed facial diplegia, and unilateral or bilateral lateral rectus palsy. Brain MRI scans showed normal and there were no definite brainstem dysfunctions on electrophysiologic studies.
Abducens Nerve Diseases
;
Adult
;
Brain
;
Brain Stem
;
Child
;
Female
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Mobius Syndrome
;
Mothers
4.Three Cases of Mobius Syndrome in a Family
Hwan Mo JEONG ; Seung Hee HONG ; Dong Jin SHIN
Journal of the Korean Neurological Association 1996;14(4):1035-1041
Mobius syndrome is generally considered to be a static disorder of congenital origin, and is manifested as unilateral or bilateral facial weakness and lateral gaze limitation. In most instances the syndrome occurs sporadically, but rarely familial cases have been reported. We report a family of three members with Mobius syndrome; a 7-year-old girl, a 6-year-old boy, and their 29-year-old mother. Each patient revealed facial diplegia, and unilateral or bilateral lateral rectus palsy. Brain MRI scans showed normal and there were no definite brainstem dysfunctions on electrophysiologic studies.
Abducens Nerve Diseases
;
Adult
;
Brain
;
Brain Stem
;
Child
;
Female
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Mobius Syndrome
;
Mothers
5.Three Cases of Mobius Syndrome in a Family
Hwan Mo JEONG ; Seung Hee HONG ; Dong Jin SHIN
Journal of the Korean Neurological Association 1996;14(4):1035-1041
Mobius syndrome is generally considered to be a static disorder of congenital origin, and is manifested as unilateral or bilateral facial weakness and lateral gaze limitation. In most instances the syndrome occurs sporadically, but rarely familial cases have been reported. We report a family of three members with Mobius syndrome; a 7-year-old girl, a 6-year-old boy, and their 29-year-old mother. Each patient revealed facial diplegia, and unilateral or bilateral lateral rectus palsy. Brain MRI scans showed normal and there were no definite brainstem dysfunctions on electrophysiologic studies.
Abducens Nerve Diseases
;
Adult
;
Brain
;
Brain Stem
;
Child
;
Female
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Mobius Syndrome
;
Mothers
6.Lesion Localization in Patients with Hyperparathyroidism Using Double-phase Tc-99m MIBI Parathyroid Scintigraphy.
Dae Hyuk MOON ; Hee Kyung LEE ; Jin Sook RYU ; Jung Woo SHIN ; Jae Seung KIM ; Seung Mo HONG ; Gyungyub GONG ; Suk Joon HONG
Korean Journal of Nuclear Medicine 1999;33(2):120-130
PURPOSE: This study was performed to evaluate the diagnostic usefulness of double-phase Tc-99m MIBI parathyroidism scintigraphy with single photon emission computed tomography (SPECT) in patients with hyperparathyroidism. We also evaluated the relationship between Tc-99m MIBI uptake and oxyphil cell contents in parathyroid glands. MATERIALS AND METHODS: The subjects were 28 parathyroid glands of 10 patients who underwent Tc-99m MIBI parathyroid scintigraphy and parathyroidectomy for clinically suspected hyperparathyroidism. Early and delayed pinhole images were obtained at 15 minutes and 2 hours after injection of Tc-99m MIBI, and SPECT images were followed. The weight and oxyphil cell contents of parathyroid of tissue were obtained from pathologic specimen, and the scintigraphic findings were compared with histopathology. RESULTS: In surgical histopathology, 6 parathyroid adenomas and 9 parathyroid hyperplasias were confirmed. The sensitivity, specificity, and positive predictive value of early and delayed images were 46.7% (7/15), 76.9% (10/13), 70% (7/10) and 667% (10/15), 92.3% (12/13), 90.9% (10/11), respectively. SPECT image detected an additional small hyperplasia. The sensitivity, specificity, and positive predictive value of combined interpretation of early and delayed images with SPECT were 733% f11/15), 100% (13/13), 100% (11/11). The sensitivity was 100% (6/6) for aenoma, whereas that was 555% (5/9) for hyperplasia. Both adenomas and hyperplasias showed significantly increased oxyphil cell contents compared with normal parathyroid glands (p<0.0001), but the oxyphil cell content and weight were not significantly different between adenomas and hyperplasias. CONCLUSION: Double-phase Tc-99m MIBI parathyroid scintigraphy with SPECT is useful for lesion localization m patients with hyperparathyroidism. Although both adenoma and hyperplasia have increased oxyphil cell content, the sensitivity is high in adenoma, but low in hyperplasia.
Adenoma
;
Humans
;
Hyperparathyroidism*
;
Hyperplasia
;
Parathyroid Glands
;
Parathyroid Neoplasms
;
Parathyroidectomy
;
Radionuclide Imaging*
;
Sensitivity and Specificity
;
Tomography, Emission-Computed, Single-Photon
7.Congenital Desmoplastic Cerebral Glioblastoma: A Case Report
Hong Il HA ; Seung Mo HONG ; Seung Koo LEE ; Shin Kwang KHANG
Korean Journal of Pathology 2002;36(6):440-444
Desmoplastic cerebral glioblastoma has been described recently and is a very rare histologic variant of glioblastoma. We report a case of congenital cerebral glioblastoma associated with intense desmoplastic stromal reaction. A male infant was born at 36 gestational weeks by Cesarian section. He had a brain tumor, which was detected by fetal ultrasonography. The tumor was partially resected 2 months after the day of the boy's birth and totally resected when he was one year old. The microscopic features of the tumor were those of glioblastoma, including high cellularity, frequent mitotic figures, vascular endothelial proliferation, and geographic palisading necrosis. The tumor showed an area of intense desmoplasia where tumor cells were surrounded by dense reticulin fibers. The desmoplastic cerebral tumors in children may be a distinct group of brain tumor, and it is important to understand the entity of these tumors which generally seem to be associated with more favorable prognosis compared to other high grade brain tumors.
Brain Neoplasms
;
Child
;
Glioblastoma
;
Humans
;
Infant
;
Male
;
Necrosis
;
Parturition
;
Prognosis
;
Reticulin
;
Ultrasonography, Prenatal
8.A Case of Esotropia Simulating Exotropia due to Large Positive Angle Kappa
Seung Mo KIM ; Jong Bok LEE ; Hong Bok KIM
Journal of the Korean Ophthalmological Society 1988;29(3):431-435
The angle kappa is defined as the angle between the optical axis and the visual axis. A positive angle kappa may simulate an exodeviation, while a negative angle kappa may simulate an esodeviation. It is measured by several methods, and ranges from 2 to 5 degrees. A 19 year old Korean male was seen in our clinic complaining of exodeviation OS, but he was found to have an esotropia OD with large positive angle kappa.
Axis, Cervical Vertebra
;
Esotropia
;
Exotropia
;
Humans
;
Male
;
Young Adult
9.A Case of Esotropia Simulating Exotropia due to Large Positive Angle Kappa
Seung Mo KIM ; Jong Bok LEE ; Hong Bok KIM
Journal of the Korean Ophthalmological Society 1988;29(3):431-435
The angle kappa is defined as the angle between the optical axis and the visual axis. A positive angle kappa may simulate an exodeviation, while a negative angle kappa may simulate an esodeviation. It is measured by several methods, and ranges from 2 to 5 degrees. A 19 year old Korean male was seen in our clinic complaining of exodeviation OS, but he was found to have an esotropia OD with large positive angle kappa.
Axis, Cervical Vertebra
;
Esotropia
;
Exotropia
;
Humans
;
Male
;
Young Adult
10.Giant Aneurysm of a Congenital Coronary Arteriovenous Fistula Arising from the Left Coronary Artery
Mi Seung SHIN ; Sun Hee MAENG ; Hye Jin LEE ; Hong Keun CHO ; Ick Mo CHUNG ; Gil Ja SHIN
Korean Circulation Journal 1999;29(7):740-746
Congenital coronary arteriovenous fistula is a rare condition which is an abnormal communication of the coronary artery with the right ventricle, right atrium, left atrium or left ventricle. Coronary artery aneurysm is an uncommon disease which is defined as coronary dilatation which exceeds the diameter of normal adjacent segments or the diameter of the patient's largest coronary vessel by 1.5 times. In young ages, symptoms are unusual, but significant symptoms and complications such as congestive heart failure, subacute bacterial endocarditis, coronary steal syndrome, aneurysm formation, rupture, and pulmonary hypertension may appear among the older age group. We report a case of giant aneurysm of a congenital coronary arteriovenous fistula between left co-ronary artery and right ventricular outflow tract with significant left to right shunt confirmed in a 84-year old female with a brief review of literature.
Aged, 80 and over
;
Aneurysm
;
Arteries
;
Arteriovenous Fistula
;
Coronary Aneurysm
;
Coronary Vessels
;
Dilatation
;
Endocarditis, Subacute Bacterial
;
Female
;
Heart Atria
;
Heart Failure
;
Heart Ventricles
;
Humans
;
Hypertension, Pulmonary
;
Rupture