2.Usefulness of 5-aminolevulinic acid-photodynamic diagnosis in lung cancer.
Korean Journal of Medicine 2009;77(5):573-575
Lung cancer remains the leading cause of cancer death despite 50 years of antismoking efforts and advances in treatment. Overall, the 5-year survival remains disappointing at 15%. The majority of lung cancers are inoperable at presentation, thereby limiting treatment options and the potential to cure. The best prognosis for lung cancer is expected when the diagnosis is made at an early stage of the disease. At present, the best way to diagnose lung cancer is a combination of three different screening tools: low-dose computed tomography (CT), sputum analyses, and fluorescence bronchoscopy. The tumor marking ability of 5-aminolevulinic acid (5-ALA) has been demonstrated. Inhalation of 5-ALA has been used to detect early lung cancer and is safe and reliable. The data of Yoon et al. in this issue describe the usefulness of photodynamic diagnosis with ALA inhalation.
Bronchoscopy
;
Fluorescence
;
Inhalation
;
Lung
;
Lung Neoplasms
;
Mass Screening
;
Prognosis
;
Sputum
3.Comparison of various DNA extraction methods for diagnosis of tuberculosis using a polymerase chain reaction.
Ju Ock KIM ; Pyo Seong HAN ; Seok Cheol HONG ; Jong Jin LEE ; Hai Jeong CHO ; Sun Young KIM
Tuberculosis and Respiratory Diseases 1993;40(1):43-51
No abstract available.
Diagnosis*
;
DNA*
;
Polymerase Chain Reaction*
;
Tuberculosis*
4.High VPP combination chemotherapy for advanced non-small cell lung cancer.
Seok Cheol HONG ; Pyo Seong HAN ; Jong Jin LEE ; Hai Jeong CHO ; Ju Ock KIM ; Sun Young KIM
Tuberculosis and Respiratory Diseases 1993;40(4):367-377
No abstract available.
Carcinoma, Non-Small-Cell Lung*
;
Drug Therapy, Combination*
5.Clinical Observation of Convulsions in Children.
Sang Chul PARK ; Eun Mi KIM ; Jae Ock PARK ; Dong Whan LEE ; Sang Ju LEE ; Sang Man SHIN
Journal of the Korean Pediatric Society 1983;26(11):1102-1110
6.A Case of MCLS Associated with Pleural and Pericardial Effusion.
Hyun Sook LEE ; Young Ok BANG ; Jae Ock PARK ; Chang Hwi KIM ; Dong Whan LEE ; Sang Ju LEE
Journal of the Korean Pediatric Society 1983;26(2):170-174
No abstract available.
Pericardial Effusion*
7.Lung Cancer Screening.
Tuberculosis and Respiratory Diseases 2006;61(3):207-213
No abstract available.
Lung Neoplasms*
;
Lung*
;
Mass Screening*
8.The reverse lip design: a design for safe and effective abdominoplasty
Ju Young GO ; Ryuck Seong KIM ; Jae Jin OCK ; Bohrham JEONG ; Seong Hwan BAE
Archives of Aesthetic Plastic Surgery 2021;27(4):153-157
Conventional abdominoplasty includes the removal of an ellipse-shaped section of abdominal tissue between the umbilicus and mons pubis. However, this method can result in tension of the undermined flap, especially in the midline. To address this problem, we present reverse lip design as a modified method that also has aesthetic advantages. The reverse lip design entails a longer lower flap edge while preserving the triangular tissue in the vascularly stable pubis area. These markings create an image of a reverse lip shape with a cleft at the bottom of the lower markings. After typical lipoabdominoplasty is performed, redundant waist tissues can easily be pulled inward and downward. The reverse lip design abdominoplasty demonstrated no complications and required no further revisions after the procedure. Patients were generally satisfied with the aesthetic improvements in their body shape. They were also able to return to their routine activities approximately 1 week after the operation while wearing a supporting undergarment. This modified abdominoplasty using the reverse lip design reduces low midline tension of the undermined abdominal flap while enhancing body aesthetics with a slimmer waistline, leading to higher patient satisfaction.
9.Once vs. Twice Daily Thoracic Irradiation in Limited Stage Small Cell Lung Cancer.
Jun Sang KIM ; Jae Sung KIM ; Ju Ock KIM ; Sun Young KIM ; Moon June CHO
The Journal of the Korean Society for Therapeutic Radiology and Oncology 1998;16(3):291-301
PURPOSE: A retrospective study was conducted comparing single daily fraction (SDF) thoracic radiotherapy (TRT) with twice daily (BID) TRT to determine the potential benefit of BID TRT in limited-stage small cell lung cancer (SCLC). Endpoints of the study were response, survival, pattern of failure, and acute toxicity. MATERIALS AND METHODS: Between November 1989 to December 1996, 78 patients with histologically proven limited-stage SCLC were treated at the Department of Therapeutic Radiology, Chungnam National University Hospital. Of these, 9 were irradiated for palliative intent, and 1 had recurrent disease. Remaining 68 patients were enrolled in this study. There were 26 patients with a median age of 58 years, and 22 (85%) ECOG performance score of less than 1 in SDF TRT. There were 42 patients with a median age of 57 years, and 36 (86%) ECOG performance score of less than 1 in BID RT. By radiation fractionation regimen, there were 26 in SDF TRT and 42 in BID TRT. SDF TRT consisted of 180 cGy, 5 days a week. BID TRT consisted of 150 cGy BID, 5 days a week in 13 of 42 and 120 cGy BID, in 29 of 42. And the twice daily fractions were separated by at least 4 hours. Total radiotherapy doses were between 5040 and 6940 cGy (median, 5040 cGy) in SDF TRT and was between 4320 and 5100 cGy (median, 4560 cGy) in BID TRT. Prophylactic cranial irradiation (PCI) was recommended for patients who achieved a CR. The recommended PCI dose was 2500 cGy/10 fractions. Chemotherapy consisted of CAV (cytoxan 1000 mg/m2, adriamycin 40 mg/m2, vincristine 1 mg/m2) alternating with VPP (cisplatin 60 mg/m2, etoposide 100 mg/m2) every 3 weeks in 25 (96%) of SDF TRT nd in 40 (95%) of BID TRT. Median cycle of chemotherapy was six in both group. Timing for chemotherapy was sequential in 23 of SDF TRT and in 3 BID TRT, and concurrent in 3 of SDF TRT and in 39 of BID TRT. Follow-up ranged from 2 to 99 months (median, 14 months) in both groups. RESULTS: Of the 26 SDF TRT, 9 (35%) achieved a complete response (CR) and 14 (54%) experienced a partial response (PR). Of the 42 BID TRT, 18 (43%) achieved a CR and 23 (55%) experienced a PR. There was no significant response difference between the two arms (p=0.119). Overall medianand 2-year survival were 15 months and 26.8%, respectively. The 2-year survivals were 26.9% and 28% in both arm, respectively (p=0.51). The 2-year survivals were 35% in CR and 24.2% in PR, respectively. The grade 2 to 3 esophageal toxicities and grade 2 to 4 neutropenias were more common in BID TRT (p=0.028, 0.003). There was no difference in locoregional and distant metastasis between the two arms (p=0.125 and 0.335, respectively). The most common site of distant metastasis was the brain. CONCLUSION: The median survival and 2-year survival were 17 months and 26.9% in SDF TRT with sequential chemotherapy, and 15 months and 28% in BID TRT with concurrent chemotherapy, respectively. We did not observe a substantial improvement of long-term survival in the BID TRT with concurrent chemotherapy compared with standard schedules of SDF TRT with sequential chemotherapy. The grade 2 to 3 esophageal toxicities and grade 2 to 4 neutropenias were more common in BID TRT with concurrent chemotherapy. Although the acute toxicities were more common in BID TRT with concurrent chemotherapy than SDF TRT with sequential chemotherapy, a concurrent chemotherapy and twice daily TRT was feasible. However further patient ccrual and long-term follow up are needed to determine the potential benefits of BID TRT in limited-stage SCLC.
Appointments and Schedules
;
Arm
;
Brain
;
Chungcheongnam-do
;
Cranial Irradiation
;
Doxorubicin
;
Drug Therapy
;
Etoposide
;
Follow-Up Studies
;
Humans
;
Neoplasm Metastasis
;
Neutropenia
;
Radiation Oncology
;
Radiotherapy
;
Retrospective Studies
;
Small Cell Lung Carcinoma*
;
Vincristine
10.A case of giant cell tumor originated from right second rib.
Seok Cheol HONG ; Pyo Seong HAN ; Nam Jae KIM ; Ju Ock KIM ; Sam Yong KIM ; Seung Pyung LIM ; Kyu Sang SONG ; Sun Young KIM
Tuberculosis and Respiratory Diseases 1992;39(2):172-175
No abstract available.
Giant Cell Tumors*
;
Giant Cells*
;
Ribs*