1.Vascularized Fibular Epiphysis and Epiphyseal Plate Transplantation
Myung Chul YOO ; Jin Hwan AHN ; Bang Seop LEE
The Journal of the Korean Orthopaedic Association 1985;20(6):1153-1156
The injury of the epiphysis or epiphyseal plate produces undesirable effects on the normal growth of the bone, such as bone bridge, growth arrest and angular deformity. Authors performed vascularized fibular epiphysis and epiphyseal plate transplantation in 7 years old girl, who received the excision of the exostosis on distal ulna, followed by progressive varus deformity of right forearm and growth arrest of distal ulna. With follow
Congenital Abnormalities
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Epiphyses
;
Exostoses
;
Female
;
Forearm
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Growth Plate
;
Humans
;
Methods
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Transplantation
;
Ulna
2.Comparison of Optic Disc Measurements between Computer-aided Morphometry and Heidelberg Retina Tomograph.
Hwan Eok YEO ; Ki Bang UHM ; Chul HONG
Journal of the Korean Ophthalmological Society 2003;44(5):1023-1028
PURPOSE: To compare optic disc measurements between computer-aided morphometry and Heidelberg Retina Tomograph (HRT). METHODS: For 59 patients with primary open-angle glaucoma and 9 subjects with ocular hypertension, measurements of the optic disc area and neuroretinal rim area were obtained using our computer-aided morphometric techniques and the HRT. RESULTS: The mean optic disc areas measured with the HRT was smaller than those with the computer-aided techniques (p=0.02). Rim area and rim area to disc area were significantly (p
3.A Case of Multiple Trichoepitheliomas and Basal Cell Carcinomas Co-existed on the Nose
Hyo Jung KIM ; Ju Hee HAN ; Chul Hwan BANG ; Jun Young LEE ; Ji Hyun LEE ; Young Min PARK
Korean Journal of Dermatology 2019;57(3):164-166
No abstract available.
Carcinoma, Basal Cell
;
Nose
4.Umbilical Polyp.
Chul Hwan BANG ; Hyun Ju LEE ; Min Ho KIM ; Sang Hyun CHO ; Jeong Duk LEE
Korean Journal of Dermatology 2010;48(11):1031-1033
An umbilical polyp is a rare congenital lesion and it represents one of the developmental anomalies of omphalomesenteric duct remnants. Clinically, an umbilical polyp presents as a red, firm and round tumor with mucoid and sometimes bloody secretions. Umbilical polyps can be mistaken clinically for other umbilical disorders such as umbilical granulomas and granuloma pyogenicum. Hisopathologically, the umbilical polyp is usually composed of small intestinal mucosa or ectopic gastrointestinal mucosa. Herein, we report on two cases of umbilical polyps:one umbilical polyp was composed of small intestinal mucosa and the other consisted of gastric mucosa.
Gastric Mucosa
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Granuloma
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Granuloma, Pyogenic
;
Intestinal Mucosa
;
Mucous Membrane
;
Polyps
;
Vitelline Duct
5.Comparison of Therapeutic Efficacy between Lateral Type of Distal and Lateral Subungual Onychomycosis (DLSO) and Non-lateral Types of DLSO.
Chul Hwan BANG ; Young Bok LEE ; Hyun Jeong PARK ; Baik Kee CHO
Korean Journal of Medical Mycology 2011;16(4):186-195
BACKGROUND: Onychomycosis is a common fungal infection accounting for 50% of all nail disorders. Above all the clinical types of onychomycosis, distal and lateral subungual onychomycosis (DLSO) is the most common clinical type seen up to 70~90% in onychomycosis patients. Even though the cure rate and recurrence rate of DLSO are considered to be different according to the clinical type of DLSO. Clinical experience, there is a few clinical study showing the difference. OBJECTIVE: This is to investigate the therapeutic efficacy of lateral type of DLSO comparing with the other types of DLSO. METHODS: We reviewed 81 DLSO cases who visited our clinic from June 1st, 2006 to June 31st, 2010, and classified them into 2 groups; lateral type and non-lateral types including edge, distal and linear type. We treated the patients with oral antifungal agent for 4 months, and followed them up in 2 months. Scoring clinical index for onychomycosis (SCIO) was checked and photography was taken before treatment and after treatment. RESULTS: There are no significant differences in average age and male to female ratio between lateral DLSO and non-lateral DLSO. The comparison of SCIO score distribution before treatment between lateral DLSO and non-lateral DLSO showed no significant statistical difference. However, there was significant change in SCIO score distribution after the treatment. Decreased SCIO score in lateral DLSO was 6.99, while non-lateral DLSO was 11.1 (p=0.018). There was 2cases worsen cases in lateral DLSO, while there was no worsen case in non-lateral DLSO (p=0.019). CONCLUSION: Lateral DLSO is more difficult to treat than non-lateral DLSO.
Accounting
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Female
;
Humans
;
Male
;
Nails
;
Onychomycosis
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Photography
;
Recurrence
6.Non-familial Acrokeratosis Verruciformis of Hopf.
Chul Hwan BANG ; Hei Sung KIM ; Young Min PARK ; Hyung Ok KIM ; Jun Young LEE
Annals of Dermatology 2011;23(Suppl 1):S61-S63
Acrokeratosis verruciformis of Hopf is a rare genodermatosis with an autosomal dominant mode of inheritance. It is a disorder of keratinization, characterized by multiple, flat-topped, skin-colored keratotic lesions resembling plane warts typically observed on the dorsum of the hands and feet. Histopathologically, the lesion shows considerable hyperkeratosis, acanthosis, and papillomatosis, mimicking a "church spire", and a thickened granular layer. It arises in early life, often at birth or infancy. Herein, we report on a rare sporadic case of acrokeratosis verruciformis of Hopf. A 44-year-old Caucasian man presented with multiple, grouped, hyperkeratotic, whitish, flat papules on his shins and feet, which had been present for more than one year. Histopathological examination showed typical findings of acrokeratosis verruciformis of Hopf. Our case is unique in that the patient had no familial history of similar skin lesions.
Adult
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Darier Disease
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Foot
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Hand
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Humans
;
Keratins
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Papilloma
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Parturition
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Skin
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Warts
;
Wills
7.Rhabdomyolysis with severe hypernatrenia.
Chul Woo YANG ; Dae Hwan JANG ; Kyung Yon O ; Kyung Han LEE ; In Suk PARK ; Yun Sik CHANG ; Young Suk YOON ; Byung Kee BANG
Korean Journal of Nephrology 1991;10(4):614-619
No abstract available.
Rhabdomyolysis*
8.Biopsy-Proven Immune Complex Glomerulonephritis Associated with Sunitinib in a Patient with a Gastrointestinal Stromal Tumor.
Hankyu LEE ; Hyang Rim LEE ; Kook Hwan OH ; Kyung Chul MOON ; Curie AHN ; Suhnggwon KIM ; Yung Jue BANG
Korean Journal of Nephrology 2010;29(5):644-649
Sunitinib, a multi-targeted tyrosine kinase inhibitor, is used for the treatment of renal cell carcinoma and gastrointestinal stromal tumors. Many adverse effects associated with sunitinib, including hypertension, proteinuria, and thrombotic microangiopathy, have been reported; however, the other forms of glomerulonephritis are very rare. We report a case of biopsy-confirmed immune complex glomerulonephritis in a patient with a gastrointestinal tumor who received sunitinib treatment. The proteinuria subsided partially after sunitinib was discontinued, but when the drug was reintroduced, it recurred.
Antigen-Antibody Complex
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Carcinoma, Renal Cell
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Gastrointestinal Stromal Tumors
;
Glomerulonephritis
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Humans
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Hypertension
;
Indoles
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Protein-Tyrosine Kinases
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Proteinuria
;
Pyrroles
;
Thrombotic Microangiopathies
9.Fate of Regurgitation of Left Atrioventricular Valve Following Repair of Atrioventricular Septal Defect.
Siho KIM ; Han Ki PARK ; Byung chul CHANG ; Bum Koo CHO ; Jung Heui BANG ; Young Hwan PARK
The Korean Journal of Thoracic and Cardiovascular Surgery 2003;36(12):961-969
BACKGROUND: The purpose of this study was to evaluate the fate of left atrioventricular valve regurgitation(LAVVR) following repair of complete atrioventricular septal defects (AVSDs). MATERIAL AND METHOD: Between July 1984 and March 2002, repair of complete AV defects were performed in 77 patients. Mean age at surgery was 30.23+/-69.11 months (range 1 to 456). Echocardiograms of all survivors after isolated AVSDs correction were reviewed. LAVVR were evaluated with color doppler echocardiography in 64 survival periodically. On each study, LAVVR severity was graded on a 1 to 4 scale, based upon the size of the regurgitated jet. RESULT: Mild deterioration of LAVV function was fairly common. LAVVR severity increased by >1 grade in 19 patients (30.2%) during the course of the study. However, the deterioration in LAVVR function occurred primarily between 12 and 24 months postoperatively. After the initial 24 postoperative months, LAVVR worsened on only 8 occasions and in each instance worsened by only 1 grade. Deterioration more than 3+ LAVVR occurred in only 3 patients. And deterioration to 4+ LAVVR was not observed after the initial 24 postoperative months but one. Survival curve analysis predicted a 88.2% of ten-year freedom rate from development of 4+ LAVVR after initial operation of complete AVSDs. CONCLUSION: Postoperative LAVVR remains fairly stable following AVSDs repair. Serious deterioration is rare after 24 postoperative months, especially after the initial 48 postoperative months. But serial follow-up study with echocariogram was need till 24 postoperative months after repair of complete AVSDs.
Echocardiography
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Echocardiography, Doppler, Color
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Follow-Up Studies
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Freedom
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Heart Defects, Congenital
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Humans
;
Survivors
10.A Case of Lepromatous Leprosy in an Elderly Patient
Seung Ah YOO ; Chul Hwan BANG ; Ju Hee HAN ; Ji Hyun LEE
Korean Journal of Dermatology 2020;58(7):487-488
Leprosy is an infectious disease caused by Mycobacterium leprae. Patients usually present with hypopigmented or erythematous plaques with central hypoesthesia or tenderness, and necessitate a differential diagnosis with eczema, granuloma annulare, sarcoidosis, syphilid, mycosis fungoides, erythema nodosum, and skin cancer. A 93-year-old woman presented with asymptomatic erythematous plaques and subdermal nodules on the face and extremities for 6∼ 7 months, and the lesions were suspicious for skin cancer. Histopathologic examination revealed diffuse infiltration of foamy histiocytes separated by a grenz zone. Acid-fast bacilli were seen in Ziehl−Neelsen stain with clumps called globi. Based on clinical and histopathological findings, she was finally diagnosed with lepromatous leprosy.The patient was diagnosed with leprosy at an advanced age; thus, we report the case in which dermatologists should consider leprosy as well as skin cancer in the elderly patients with unusual erythematous nodules, despite decreasing prevalence of leprosy.