1.The Therapeutic Effect of Nail Splinting in Ingrown Toenails.
Hwi Jun KIM ; Dong Ju HA ; Woo Young SIM ; Mu Hyoung LEE ; Choong Rim HAW ; Nack In KIM
Korean Journal of Dermatology 2001;39(8):855-860
BACKGROUND: Ingrown toenail is one of the most common nail complaints. It occurs chiefly on the great toes, where there is an excessive lateral nail growth into the nail fold, leading to painful irritation, inflammation, infection, and growth of excessive granulation tissue. Many treatments have been described, but these classic treatment modalities may lead to severe damage of the nail fold or to frequent relapses. OBJECTIVE: We attempted to evaluate the therapeutic effect of nail splinting which is a noninvasive therapy for ingrown toenails. METHODS: A total of 64 patients(78 lesions) with ingrown toenails were enrolled in the study. The lateral edge of the nail plate including the spicule is splinted with a lengthwise-incised flexible plastic tube. The efficacy of nail splinting for ingrown toenail was assessed by analyzing the degrees of post-treatment pain and a recurrence rate. RESULTS: 1.The average age of the patients was 37 years old. There were 38 male patients(47 lesions) and 26 female patients(31 lesions). The right big toe was affected in 27 patients and the left big toe in 23 patients. Fourteen patients had both feet affected at the same time. 2.The pain all cleared in an average 2.3 days of treatment. Other problems such as redness, swelling and granulation tissue gradually decreased as time went by. 3.There was a 7.8% recurrence rate at six months after the procedure. CONCLUSION:We recommend nail splint as an alternative to traditional treatment for ingrown toenail because it is simple and easy to perform, noninvasive, effective, well tolerated, and does not require any special equipment.
Adult
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Female
;
Foot
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Granulation Tissue
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Humans
;
Inflammation
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Male
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Nails*
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Naphazoline
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Plastics
;
Recurrence
;
Splints*
;
Toes
2.A Case of Warfarin-Induced Intramural Hematoma Diagnosed by Double-Balloon Enteroscopy.
Dong Hwi RIM ; Chang Soo EUN ; Shin Jae MOON ; Jung Ho BAE ; Tae Yeob KIM ; Hang Lak LEE ; Joo Hyun SOHN ; Yong Cheol JEON ; Dong Soo HAN
Intestinal Research 2011;9(2):162-165
Although bleeding is a major complication of oral anticoagulant therapy, warfarin-induced spontaneous intramural hematoma of the small bowel is a very rare complication. The clinical features of spontaneous intramural hematoma vary from mild abdominal pain to panperitonitis due to bowel perforation. Because spontaneous intramural hematoma can proceed to a life threatening situation, early diagnosis is of vital importance. Although there are a number of radiologic diagnostic tools available including abdominal ultrasonography and computed tomography, confirmation of the diagnosis through direct visualization of the involved bowel mucosa is very helpful. Direct confirmation of warfarin-induced spontaneous intramural hematoma of the small bowel is possible using double-balloon enteroscopy. We report a case of warfarin-induced spontaneous intramural hematoma with a review of the relevant literature.
Abdominal Pain
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Double-Balloon Enteroscopy
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Early Diagnosis
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Hematoma
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Hemorrhage
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Mucous Membrane
3.Systemic Sclerosis Coincidence with Sarcoidosis: A Case Report and Review of the Literature.
Dong Chan KIM ; Dong Hwi RIM ; Young Taek KIM ; Joo Yeon KO ; Chan Kum PARK ; Sung Soo PARK ; Jae Bum JUN
The Journal of the Korean Rheumatism Association 2010;17(4):400-405
A 62-year-old Korean woman was admitted to our department to evaluate a chronic cough and sputum, which had begun several weeks ago. The patient had been diagnosed with systemic sclerosis in 2004. Autoantibody screening tests were negative for the anticentromere and antitopoisomerase antibodies. She received therapy with combined cyclophosphamide, a calcium channel blocker, D-penicillamine, and low dose steroid. In 2006, a pulmonary function test (PFT) showed a restrictive pattern, and a computed tomography (CT) scan of the lungs revealed interstitial lung disease, but no symptoms were present, so we maintained her on the medication. In October 2008, a chest x-ray and CT scan of the lungs demonstrated aggravation with bilateral basal interstitial infiltrates and hilar lymphadenopathy. Cyclophosphamide pulse therapy was conducted six times during 6 months, but there was no change on her chest CT and PFT, and she had no symptoms, so we decided to follow up. On admission, no significant interval change in the reticular opacity of both lower lungs was observed, but several lymph nodes were enlarged on a chest and neck CT. The skin showed multiple large polygonal-shaped scaled lesions on her upper and lower extremities. Biopsies were taken from the skin of the lower extremities and the left cervical lymph node. Typical non-caseating granulomas corresponding to sarcoidosis were found along with systemic sclerosis findings.
Antibodies
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Biopsy
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Calcium Channels
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Cough
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Cyclophosphamide
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Female
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Follow-Up Studies
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Granuloma
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Humans
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Lower Extremity
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Lung
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Lung Diseases, Interstitial
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Lymph Nodes
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Lymphatic Diseases
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Mass Screening
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Middle Aged
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Neck
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Penicillamine
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Respiratory Function Tests
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Sarcoidosis
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Scleroderma, Systemic
;
Skin
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Sputum
;
Thorax
4.A Case of Spondyloepiphyseal Dysplasia Tarda (SEDT) Misdiagnosed as Ankylosing Spondylitis.
Il Hwan OH ; June Seok SONG ; Dong Hwi RIM ; Jong Wook CHOI ; Seunghun LEE ; Joo Hyun LEE ; Tae Hwan KIM
Journal of Rheumatic Diseases 2011;18(4):311-314
The spondyloepiphyseal dysplasia tarda (SEDT) is a hereditary arthropathy that progressively leads to deformities of small and large joints, irregularities of the end plates of vertebral bodies, which causes joint restriction, short stature, and gait difficulties. The typical radiographic findings of SEDT are generalized platyspondyly and dysplasia of the epiphyses, resulting in premature arthrosis. Clinically SEDT is manifested as a form of short-trunk dwarfism and early arthrosis in the period from late childhood to adolescence. The major clinical importance of this rare disease is similarity to juvenile idiopathic arthritis (JIA), which has a rather different prognosis and treatment. A few cases of SEDT have been published. However, no cases have been reported in South Korea. We describe the case of a 29-year old man who suffered from back and multiple joint pain, who was misdiagnosed as having ankylosing spondylitis. We evaluated the patient clinically and radiographically in greater detail, and changed his diagnosis to SED tarda.
Adolescent
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Arthralgia
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Arthritis, Juvenile Rheumatoid
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Congenital Abnormalities
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Dwarfism
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Epiphyses
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Gait
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Humans
;
Joints
;
Osteochondrodysplasias
;
Prognosis
;
Rare Diseases
;
Republic of Korea
;
Spondylitis, Ankylosing
5.A Case of Klinefelter's Syndrome Accompanying with Polymyositis.
Min Kyu LEE ; Byung Sik KIM ; Suk Hyun JUNG ; Gun Hwa LEE ; Jin Ok KIM ; Dong Hwi RIM ; Yu Hwa LEE ; Woong Jun KIM ; So Young BANG ; Hye Soon LEE
Journal of Rheumatic Diseases 2012;19(3):152-155
Klinefelter's syndrome which is characterized by hypogonadism with karyotype abnormality (47 XXY or 46 XY/47 XXY) in males has been reported to be associated with autoimmune diseases including rheumatoid arthritis and systemic lupus erythematosus. However, Klinefelter's syndrome accompanying with polymyositis has rarely been reported. We report a case of KFS with polymyosits in a 38-year old man for the first time in Korea.
Arthritis, Rheumatoid
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Autoimmune Diseases
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Humans
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Hypogonadism
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Karyotype
;
Klinefelter Syndrome
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Korea
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Lupus Erythematosus, Systemic
;
Male
;
Polymyositis