1.A clinical review of upper gastrointestinal bleeding.
Young Hwan CHO ; Joon Heon JEONG ; Il Dong CHUNG
Journal of the Korean Surgical Society 1991;41(2):159-167
No abstract available.
Hemorrhage*
2.Leiomyoma of the Ovary A report of two cases.
Jeong Hae KIE ; Tai Seung KIM ; Dong Hwan SHIN
Korean Journal of Pathology 1999;33(7):529-532
Ovarian leiomyoma is a rare form of the ovarian mesenchymal neoplasm and about 50 cases have been reported in the literature. It is believed that many cases may go unnoticed because they are usually small in size and frequently mistaken for the more common fibroma or fibrothecoma. Its origin is still controversial and many possibilities are considered including the smooth muscle in the blood vessel wall of the hilum or the multipotential ovarian stromal cell. Herein we describe two cases of ovarian leiomyoma with its characteristic histologic finding.
Blood Vessels
;
Female
;
Fibroma
;
Leiomyoma*
;
Muscle, Smooth
;
Ovary*
;
Stromal Cells
3.A Histopathologic, Histochemical and Immunocytochemical Study of Cardiac Myxoma.
Dong Hwan SHIN ; Hee Jeong AHN ; In Joon CHOI
Korean Journal of Pathology 1987;21(2):75-81
The immunoreactivities of surgically removed 16 cardiac myxomas were studies for factor VIII-related Ag (F VIII-RA), Ulex europaeus agglutinin I (UEA-I) and desmin alpha1-antichymotrypsin, and this study was accompained by a clinicopathologic review. More than 50% of the patients with cardiac myxomas were in their fourth and fifth decades, and cardiac myxomas were much more common in women than in men. All but on occurred in the left atrium, and the majority were attached to the atrial septum, usually in the region corresponding to the fossa ovalis. In one case, an atrial myxoma recurred 37 months after the initial excision. Microscopically, the myxomas contained a myxoid matrix composed of acid mucopolysaccharides within which were embedded polygonal cells. The cells forming both the surface and complicated vascular like channels throuhout the myxoid stroma tested positive for F VIII-RA and UEA-I. The outer cell layers of the complex vascular structures demonstrated variable staining for F VIII-RA, while isolated bundles of smooth muscle cells were present and stained for desmin. A small number of the so-called myxoma cells, immunoreactive for alpha1-antichymotrypsin which were not laden with hemosiderin pigment but were similar to histiocytes, were present particularly around the areas of hemorrhage. These findings support the current view that cellular and histologic heterogeneity arose from the divergent differentiation of multipotential mesenchymal cells. In particular, it remains to be confirmed by further study whether or not true histiocytic differentiation occurs.
Female
;
Male
;
Humans
4.Operative Treatment for Cubital Tunnel Syndrome
Kyu Cheol SHIN ; In Whan CHUNG ; Dong Heon KIM ; Jeong Hwan OH ; Sung Tae LEE ; Eui Hwan AHN ; Deok Hwan KOH
The Journal of the Korean Orthopaedic Association 1996;31(4):825-832
Thirteen patients were operated for cubital tunnel syndrome and followed for an average of 26 months postoperatively. Ten patients had a history of relevant trauma and three patients had degenerative osteoarthritis of the elbow. The average duration of symptoms was 18 months (range, 2 to 96 months). Diagnosis was made by physical examination, electromyography and nerve conduction study. Among these, nerve conduction study was found to be the most valuable diagnostic method for the patients with atypical clinical findings. Most of the operations were performed by anterior transposition of the ulnar nerve. At the most recent follow-up, the result was excellent in two patients, good in eight, and fair in three; thus ten patients(77%) showed satisfactory results. The rating system for ulnar neuropathy based on sensory, motor dysfunction and pain was useful for evaluating the operative results. The postoperative gain of score for pain and sensory function were larger than that of motor function. Factors known to influence the result of the operation (age, duration of symptom, history of trauma, method of operation) did not effect the outcome in this study. For successful operation, the ulnar nerve must be thoroughly examined, all possible levels of compression must be released and new foci of compression must be created.
Cubital Tunnel Syndrome
;
Diagnosis
;
Elbow
;
Electromyography
;
Follow-Up Studies
;
Humans
;
Methods
;
Neural Conduction
;
Osteoarthritis
;
Physical Examination
;
Sensation
;
Ulnar Nerve
;
Ulnar Neuropathies
5.A Case of Congenital Renal Anomalies in Tuner's Syndrome.
Jeong Bok LEE ; Sook Kyeung JUNG ; Dong Hwan CHO ; Won Jae PARK ; Dong Sun PARK
Journal of the Korean Pediatric Society 1984;27(6):616-620
No abstract available.
6.A Case of Congenital Ateriovenous Malformation.
Sook Kyeung JUNG ; Dong Hwan CHO ; Jeong Bok LEE ; Won Jae PARK ; Kyeung Soo PARK
Journal of the Korean Pediatric Society 1983;26(10):1029-1032
No abstract available.
7.The relationship between the TMJ internal derangement state including rotational displacement and perforation and the clinical characteristics.
Hwan Seok JEONG ; Dong Soo YOU
Journal of Korean Academy of Oral and Maxillofacial Radiology 1998;28(1):205-213
This study was designed to reveal the correlationship between the internal derangement state of TMJ and clinical characteristics including pain and mandibular dusfuntion. One hundred and twenty five subjects with TMJ signs and symptoms were chosen for two years. The level of pain and mandibular dysfuntion were evaluated by Visual Analog Scale(VAS) and Craniomandibular Index(CMI). The diagnostic categories of TMJ internal derangement were determined by arthrography and they included normal disc position, anterior disc displacement with reduction(ADDR), rotational disc displacement with reduction(RDDR), andterior disc displacement without reduction(ADDNR), and rotational disc displacement without reduction(RDDNR). Also disc perforation was used as a criteria to divide the diagnostic subgroups. The obtained results were as follows ; 1. The patient distribution of each group was 5 in normal disc position(4%), 40 in ADDR(32%), 30 in RDDR(24%), 34 in ADDNR(27%), and 16 in RDDNR(13%). 2. Perforation was observed in 8% of ADDR, 10% of RDDR, 32% of ADDNR, and 19% of RDDNR. 3. CMI of perforation group was higher than that of reduction or normal group(P<0.005), but vas showed no significant difference. 4. CMI of non-reduction group was higher than that of non-perforation group in reduction group(P<0.05). 5. There were no significant differences of CMI and VAS between anterior disc displacement group and rotational disc displacement group in both reduction and non-reduction group. 6. CMI of RDDNR group was higher than that of RDDR group(P<0.05). 7. There were no significant difference of CMI and VAS between bilateral involvement group and unilateral involvement group(p>0.05).
Arthrography
;
Humans
;
Temporomandibular Joint*
8.A Pathological Review of Pleural Effusion by Immunocytochemical Methods.
Dong Hwan SHIN ; Hee Jeong AHN ; Woo Ick YANG ; In Joon CHOI
Korean Journal of Pathology 1990;24(4):476-481
An unequivocal diagnosis of mesothelioma during life, on the basis of limited biopsy tissue or cytological specimens, is frequently difficult and requires distinction from inflammatory mesothelial hyperplasia on the one hand and secondary neoplasms, especially adenocarcinoma on the other. Although some studies have produced conflicting results, it is generally believed that immunohistochemical methods can aid in this distinction. To obtain comparable and reproducible results, 23 metastatic carcinoma of the pleura and 2 unequivocal malignant epiehtlial mesotheliomas were studied by the peroxidase-antiperoxedase method on paraffin-embedded cell blocks, and commercially available antibodies to carcinoembryonic antigen (CEA), keratin and epithelial membrane antigen (EMA) were used. Nineteen metastaic adenocarcinoma (73%) and two mesotheliomas (100%) reacted with keratin and EMA antibodies. Nineteen matastatic adenocarcinomas (73%) reacted with EMA antibodies. Nineteen metastatic adenocarcinoma (73%) reacted with CEA antibody; no mesotheliomas stained for CEA. Two cases of reactive mesothlial hyperplasia showed positive for keratin, but negative reaction for EMA and CEA. Noen of the antibodies used in this study was specific for mesothelioma, but CEA was found to be the most useful marker for differentiating between mesothelioma and metastatic carcinoma.
Adenocarcinoma
;
Biopsy
;
Neoplasm Metastasis
9.A Pathological Review of Pleural Effusion by Immunocytochemical Methods.
Dong Hwan SHIN ; Hee Jeong AHN ; Woo Ick YANG ; In Joon CHOI
Korean Journal of Pathology 1990;24(4):476-481
An unequivocal diagnosis of mesothelioma during life, on the basis of limited biopsy tissue or cytological specimens, is frequently difficult and requires distinction from inflammatory mesothelial hyperplasia on the one hand and secondary neoplasms, especially adenocarcinoma on the other. Although some studies have produced conflicting results, it is generally believed that immunohistochemical methods can aid in this distinction. To obtain comparable and reproducible results, 23 metastatic carcinoma of the pleura and 2 unequivocal malignant epiehtlial mesotheliomas were studied by the peroxidase-antiperoxedase method on paraffin-embedded cell blocks, and commercially available antibodies to carcinoembryonic antigen (CEA), keratin and epithelial membrane antigen (EMA) were used. Nineteen metastaic adenocarcinoma (73%) and two mesotheliomas (100%) reacted with keratin and EMA antibodies. Nineteen matastatic adenocarcinomas (73%) reacted with EMA antibodies. Nineteen metastatic adenocarcinoma (73%) reacted with CEA antibody; no mesotheliomas stained for CEA. Two cases of reactive mesothlial hyperplasia showed positive for keratin, but negative reaction for EMA and CEA. Noen of the antibodies used in this study was specific for mesothelioma, but CEA was found to be the most useful marker for differentiating between mesothelioma and metastatic carcinoma.
Adenocarcinoma
;
Biopsy
;
Neoplasm Metastasis
10.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
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Adult
;
Brain
;
Brain Stem
;
Child
;
Female
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Mobius Syndrome*
;
Mothers