1.Relationships between Nailfold Plexus Visibility and Clinical Variables in Adult Schizophrenics.
Dae Yeob KANG ; Hi Yeoul CHANG ; Sung Suk KANG
Journal of the Korean Society of Biological Psychiatry 1999;6(1):111-118
OBJECTIVES: There have been several evidences that the central nervous system defect is one of the etiologic factors in schizophrenia and high nailfold plexus visibility can reflect indirectly. These are particularly related to the negative symptoms of schizophrenia. In this study, we examined the relationship between nailfold plexus visibility and various clinical variables in schizophrenia. METHODS: Forty patients(20 males, 20 females) satisfying the DSM-IV criteria for schizophrenia and forty normal controls(20 males, 20 females) were measured for Plexus Visualization Score(PVS) by using capillary microscopic examination. We used Positive and negative Syndrome Scale(PANSS). Uimann-Giovannoni Process-Reactive Questionnaire(PRQ), Phillips Premorbid Adjustment Scale(PAS). Continuous Performance Test, and Backward Masking for psychopathology and clinical variables. RESULTS: There was no significant relationship between schizophrenic subjects and normal controls in PVS. PVS was correlated with PANSS positively except negative symptom subscore. PVS was correlated with PRQ score negatively, and with PAS score positively. CONCLUSIONS: This study shows high PVS are associated with more severe psychotic symptoms and with clinical variables, such as disease process and premorbid adjustment, in some schizophrenics.
Adult*
;
Capillaries
;
Central Nervous System
;
Diagnostic and Statistical Manual of Mental Disorders
;
Humans
;
Male
;
Masks
;
Psychopathology
;
Schizophrenia
2.A case of leukemia cutis in acute megakaryoblastic leukemia.
Jung OH ; Chang Suk KANG ; Sang In SHIM ; Sun Moo KIM
Korean Journal of Clinical Pathology 1992;12(4):467-471
No abstract available.
Leukemia*
;
Leukemia, Megakaryoblastic, Acute*
3.Acetabular Revision with Hemispherical Porous Coated Prosthesis.
Chang Dong HAN ; Ki Won KANG ; Woo Suk LEE
The Journal of the Korean Orthopaedic Association 1999;34(1):23-30
PURPOSE: To report the results of acetabular revisions performed with the cementless, hemi-spherical porous coated component supported by viable host bone and minimal allobone graft for acetabular deficiencies. MATERIALS AND METHODS: A retrospective study was completed for 22-revision acetabular components, using the cementless hemispherical porous coated prosthesis and minimal femoral head allograft. There was an average follow up of 48 months, with a range of 24 to 84 months. Radiographic measurements were performed in several aspects; cup-allograft contact, inclination, vertical and horizontal migration of acetabular cup, and acetabular zone by modified zone of DeLee and Charnley, in which location, size and progression or non-progression of radiolucent zone were recorded. The acetabular deficiencies were classified by the American Academy of Orthopaedic Surgeons Committee and were type I in 2 hips (9%), type II in 12 hips (55%), and type III in 8 hips (36%). Twenty acetabular cup cases of Harris-Galante II were used in this study, 1 case of Harris- Galante I, and 1 case of Duraloc. The average size of the cup was 57(44-66) mm. RESULTS: The average cup-allograft contact was 72.5% in 19 cases and we could not differentiate the margin between the host bone and the allograft in 3 cases. There was no significant vertical or horizontal migration of acetabular cup. Radiolucent zones in follow-up radiographs were 8 cases in zone IA, 4 cases in zone IB, 4 cases in zone IIB, 9 cases in zone IIC, 8 cases in zone IIIA, and 7 cases in zone IIIB. One case showed 2 mm radiolucent area in zone IIC and another case showed 3 mm radiolucent area in zone IIB, but the radiolucencies were not progressive. The remaining cases showed less than 0.5 mm radiolucent area or no radiolucent zone. The average period of bony incorporation was 13.1 months. CONCLUSIONS: We suppose that acetabular revision with the cementless hemispherical porous coated cup supported by viable host bone and minimal bone graft produces good results.
Acetabulum*
;
Allografts
;
Follow-Up Studies
;
Head
;
Hip
;
Prostheses and Implants*
;
Retrospective Studies
;
Transplants
4.A case of neonatal hemolytic disease due to anti-c isoimmunization.
Hwan Sup KANG ; Hyo Sup JOO ; Chong Woo BAE ; Suk Chul KANG ; Chang Il AHN
Journal of the Korean Pediatric Society 1982;25(9):945-948
No abstract available.
Primary Myelofibrosis*
5.Metastatic Carcinoma of the Vermiform Appendix: A Report of A Case.
Ki Hwa YANG ; Chang Suk KANG ; Suck Jin KANG ; Sun Moo KIM
Korean Journal of Pathology 1985;19(2):250-254
Though the primary carcinoma of the vermiform appendix is rare, the secondary carcinoma of the vermiform appendix is extremely rare. About fourty cases have been reported through the world. The breast is most common primary site, and adenocarcinoma is most common form. The metastatic carcinoma of the vermiform appendix, from squamous cell carcinoma of the uterine cervix, were extremely rare. The authors experienced a case of metastatic squamous cell carcinoma of the vermiform appendix, in thirty-two years old housewife. She was diagnosed with carcinoma of the uterine cervix on December, 1983, and treated with a radical hysterectomy on February, 1984, at Chicago, and with a radiation therapy. She had been suffered from palpable masses on left axilla and left neck region, and and coughing and chest pain. After an excision biopsy, on August, 1984, she showed intestinal obstruction sign including abdominal distension with abdominal pain. A right-sided hemicolectomy was performed on November, 1984. During gross examination, the wall of the distal portion of the vermiform appendix was moderatery thickened, and showed homogeneous light yellow cut surface. On microscopic examination, there were clusters of tumors that had negative stained preparations. On electron microscopic examination, the secretory granules were not found, and the characteristics of squamous cells, including intercellular spaces, desmosomes and tonofibrils, were noted.
Adenocarcinoma
;
Neoplasm Metastasis
6.Clinical Features in Adult Schizophrenics with Minor Physical Anomalies.
Dae Yeob KANG ; Seong Suk KANG ; Hi Yeoul CHANG
Korean Journal of Psychopharmacology 1999;10(1):57-64
OBJECTIVE: There have been several evidences that the central nervous system deflect is one of the etiologic factor in schizophrenia and minor physical anomalies can reflect these deflects indirectly. These central nervous deflects are particularly related to the negative symptoms of schizophrenia. In this study, we examined the relationship between minor physical anomalies and psychopathology in schizophrenia. METHODS: Forty-four patients(22 males, 22 females) satisfying the DSM-IV criteria for schizophrenia were measured for minor physical anomalies by using Waldrop Anomaly Scale(WS) and we used Positive and Negative Syndrome Scale(PANSS), Ulmann-Giovannoni Process-Reactive Questionnaire(PRQ), and Phillips Premorbid Adjustment Scale(PAS) for evaluating psychopathology and clinical variables. RESULTS: Schizophrenic patients had a higher group mean WS score than that found in the control group. Score of WS was correlated with PANSS and PAS score positively, and with PRQ score negatively. CONCLUSION: This study shows minor physical anomalies are associated with clinical variables with regard to symptom severity, poor premorbid adjustment and process of illness in at least some schizophrenics.
Adult*
;
Central Nervous System
;
Diagnostic and Statistical Manual of Mental Disorders
;
Humans
;
Male
;
Psychopathology
;
Schizophrenia
7.Calcium Pyrophosphate Dihydrate Crystal Deposition Disease (Pseudogout) of the Elbow Presenting as A Tumor-Like Mass.
Eun Deok CHANG ; An Hi LEE ; Je Hoon LEE ; Chang Suk KANG
Korean Journal of Pathology 2002;36(5):362-363
No abstract available.
Calcium Pyrophosphate*
;
Calcium*
;
Elbow*
8.Paneth Cell-rich Carcinoma of the Stomach: A case report .
Ah Won LEE ; Young Shin KIM ; Kyo Young LEE ; Chang Suk KANG ; Sang In SHIM
Korean Journal of Pathology 1998;32(8):613-615
Paneth cell-rich carcinoma is essentially an adenocarcinoma with a predominance of Paneth cells. A 60-year-old male patient was admitted with a history of abdominal distension for several months. Endoscopic examination revealed a large ulceroinfiltrative tumor involving most of the areas of the stomach. The biopsy of the lesion confirmed poorly differentiated adenocarcinoma and total gastrectomy was followed. The submitted total stomach contained a diffuse infiltrative Borrmann type IV mass with ulceration, 8.0 3.5 cm, at the body along the lesser curvature. Microscopically, it was composed of Paneth cell differentiated cancer cells and poorly differentiated tubular adenocarcinoma cells. The Paneth cell differentiation was characterized by cytoplasmic coarse eosinophilic granules, which were PAS-positive and positive reaction for lysozyme. Electron microscopic examination showed numerous, spherical, electron-dense, homogeneous granules corresponding to those in Paneth cells as well as mucin granules in the signet-ring cells, and various intermediate forms in some cancer cells, which might be immature in the Paneth cell lineage.
Adenocarcinoma
;
Biopsy
;
Cell Differentiation
;
Cell Lineage
;
Cytoplasm
;
Eosinophils
;
Gastrectomy
;
Humans
;
Male
;
Middle Aged
;
Mucins
;
Muramidase
;
Paneth Cells
;
Stomach*
;
Ulcer
9.A Case of Systemic Lupus Erythematosus Presented with Clinical Feature Resembling Multiple Sclerosis.
Chang Wan HAN ; Hoon Suk CHA ; Seong Wook KANG ; Yoon Jong LEE ; Yeong Wook SONG
The Journal of the Korean Rheumatism Association 1997;4(2):180-184
Systemic lupus erythematosus is a connective tissue disease which can affect every organ system. Neurologic abnormalities are common, occuring in approximately half of all patients at some time during the course of their illness. But symptoms of nervous system as the sole presenting symptoms occur in less than 1% of lupus patients. In patients initially presenting with neurologic symptoms and signs, differential diagnosis is difficult and sometimes it may be misdiagnosed. Therefore extensive laboratory investigations should be carried out in all patients with unusual neurological symptoms, since early diagnosis of lupus can help in providing effective treatment. We report a patient with systemic lupus erythematosus who presented with dysarthria and dysphagia resembling multiple sclerosis.
Connective Tissue Diseases
;
Deglutition Disorders
;
Diagnosis, Differential
;
Dysarthria
;
Early Diagnosis
;
Humans
;
Lupus Erythematosus, Systemic*
;
Multiple Sclerosis*
;
Nervous System
;
Neurologic Manifestations
10.Dendriform Pulmonary Ossification: A case report.
Chan Kwon JUNG ; Kyo Young LEE ; Chang Suk KANG ; Sang In SHIM ; Byung Kee KIM
Korean Journal of Pathology 2000;34(11):950-952
The dendriform pulmonary ossification (DPO) is a rare condition of unknown origin in which branching mature bony spicules, usually containing marrow, are found within the alveolar septa. DPO manifests slow progression over many years or may remain unchanged; spontaneous regression has not been recorded. Most patients have no symptoms directly attributed to the ossification, although they may have symptoms due to the underlying fibrotic process. We experienced a case of DPO in 38 year-old-man who presented with cough and sputum for a month. The chest X-ray showed marked coarsened interstitial lung markings in both lungs, especially in the lower lobes. Open lung biopsy was done. Grossly, there were significant dendriform osseous structures. Histologically, branching arrays of mature bone were found in the interstitium and occasionally in alveolar spaces. Some bony trabeculae contained fatty or cellular marrow. The alveolar septa showed fibrous thickening with chronic inflammation. The transition between fibrosis and bone tissue was observed. Our case suggests that dendriform pulmonary ossification may be a rare special manifestation of chronic fibrosing interstitial inflammation of the lung. Osseous structures seem to derive from metaplastic bone formation in the vicinity of undergoing fibrous process.
Biopsy
;
Bone and Bones
;
Bone Marrow
;
Cough
;
Fibrosis
;
Humans
;
Inflammation
;
Lung
;
Lung Diseases, Interstitial
;
Osteogenesis
;
Sputum
;
Thorax