1.Multiple Pyogenic Granulomas within Port-Wine Stain.
Sung Woo LEE ; Hyo Chan JANG ; Hyun CHUNG
Annals of Dermatology 2004;16(4):201-203
No abstract available.
Granuloma, Pyogenic*
;
Port-Wine Stain*
2.Statistical Observation for Pediatric Inpatients.
Keun Chan SOHN ; Sung Sook CHO ; Kwang Chan DOH ; Yong CHOI ; Ki Sub CHUNG ; Dong Hyuk KUM ; Sung Taek KIM
Journal of the Korean Pediatric Society 1984;27(1):1-8
No abstract available.
Humans
;
Inpatients*
3.Total Hip Arthroplasty for Ankylosed Hip
Il Yong CHOI ; Sung Chan KIM ; Hyun Kee CHUNG ; Sung Joon KIM
The Journal of the Korean Orthopaedic Association 1989;24(6):1673-1677
The conversion of the ankylosed hip to a total hip arthroplasty may be indicated if a fused hip causes low back pain, pain in the ispilateral knee, or a fibrous ankylosis is painful. Fifteen hips converted to total hip arthroplasty between Aug., 1982 and Jul., 1988 have been reviewed one to seven years after operation and the results are as follows:1. Among the 15 hips, 8 cases confirmed as fibrous ankylosis and 7 cases confirmed as bony ankylosis. 2. The causes of ankylosis is as follow tuberculous arthritis(4 cases), secondary osteoarthritis due to pyogenic hip(4 cases), rheumatoid arthritis(4 cases), post-traumatic arthritis secondary to central fracture-dislocation of hip(2 cases), and ankylosing spondylitis(1 cases). 3. The duration of immobility of the involved hip ranged from two to twenty-five years. 4. In the 14 patients, three complained of low back pain, five of ipsilateral knee pain and six of ipsilateral hip pain. 5. The lower back pain due to malposition was relieved in all cases except ankylosing spondylitis, and the pain in ipsilateral knee was also relived in all cases after hip arthroplasty. 6. The average Harris score of the fifteen hips before arthroplasty and after was 50.1 and 88.1.
Ankylosis
;
Arthritis
;
Arthroplasty
;
Arthroplasty, Replacement, Hip
;
Hip
;
Humans
;
Knee
;
Low Back Pain
;
Osteoarthritis
;
Spondylitis, Ankylosing
4.A Case of Cronkhite-Canada Syndrome.
Sung Tae CHUNG ; Eul Chang CHUNG ; Jee Ho CHOI ; Kyung Jeh SUNG ; Kee Chan MOON ; Jai Kyoung KOH
Korean Journal of Dermatology 1999;37(3):381-385
The Cronkhite-Canada syndrome is a rare, non-neoplastic, non-hereditary condition which consists of gastrointestinal polyposis associated with alopecia, onychodystrophy and hyperpigmentation of the skin. It usually encountered with severe diarrhea, weight loss and other malabsorption symptoms. The etiology of the condition is unknown. Usually, this syndrome is associated with a poor prognosis due to the effect of malabsorption and generalized debility. We report a case of this syndrome showing unusually rapid improvement after 3-month following only conservative treatment. To our knowledge, this is the first case report of Cronkhite-Canada syndrome in the Karean dermatologic literature.
Alopecia
;
Diarrhea
;
Hyperpigmentation
;
Intestinal Polyposis*
;
Prognosis
;
Skin
;
Weight Loss
6.Extended thymectomy in myasthenia gravis.
Kwang Jo CHO ; Hyung Ryul LEE ; Jong Won KIM ; Hwang Kiw CHUNG ; Si Chan SUNG
The Korean Journal of Thoracic and Cardiovascular Surgery 1992;25(12):1516-1522
No abstract available.
Myasthenia Gravis*
;
Thymectomy*
7.A Case of Oculopharyngeal Muscular Dystrophy.
Min Ho KIM ; Sung Kun CHUNG ; Chan PARK
Journal of the Korean Ophthalmological Society 1991;32(12):1153-1158
Oculopharyngeal muscular dystrophy, one of the variants of chronic progressive external ophthalmoplegia, is a disorder characterized by progressive bilateral ptosis, immobility of the eyes and dysphagia. We have experienced a 46-year-old woman complaining of bilateral ptosis, mild dysphagia and immobility of the eyes. Oculopharyngeal muscular dystrophy was confirmed by clinical, electromyographic and histopathologic examination. Therefore, we report a case of oculopharyngeal muscular dystrophy with review of literatures.
Deglutition Disorders
;
Female
;
Humans
;
Middle Aged
;
Muscular Dystrophy, Oculopharyngeal*
;
Ophthalmoplegia, Chronic Progressive External
8.Primary system amyloidosis.
Joon CHUNG ; Won Soo LEE ; Sung Ku AHN ; Soo Chan KIM
Korean Journal of Dermatology 1993;31(6):963-967
Amyloidosis is a disease complex associated with deposition of inscluble fibrillar protein in vnrious tissues of the body. Since the term, amyloidosis was first introduced by Virchow in 1853, there have been many reports in English literature, but only a few cases of iriinary systemic amyloidosis have been reported in Korea. A 56-year-old male was seven for facial purpuras, macroglossia, myilgia and arthralgia for 5 years. Histologically, the skin biopsy specimen showed amorphous, faintly eosinophilic and fissured masses of amyloid in the upper dermis that demonstrated characteristic green brefringence on Congo red staining when viewed under polarized light. Electron microscopic exanintion showed that nonbranching and nonanastomosing straigh. fibrils are irregularly arranged arouned tlie collagen fibers. Therefore, he was diagncsed with primary systemic amyloidsis by the characteristic clinical, histopathologic and ultrastructural findings.
Amyloid
;
Amyloidosis*
;
Arthralgia
;
Biopsy
;
Collagen
;
Congo Red
;
Dermis
;
Eosinophils
;
Humans
;
Korea
;
Macroglossia
;
Male
;
Middle Aged
;
Purpura
;
Skin
9.Foot salvage procedure usng saphenous ven graftin schemc vascuar disease.
Seok Chan EUN ; Woo Sung CHO ; Tae Seok ROH ; Jin Sik BURM ; Chul Hoon CHUNG
Journal of the Korean Society of Plastic and Reconstructive Surgeons 2000;27(1):35-39
Diabetic and nondiabetic vascular diseases cause significant foot problems and it frequently progress to osteomyelitis and amputation. Advances in vascular surgical techniques, including distal arterial bypass via synthetic grafts or autogenous vein grafting have opened the way for higher rate of limb salvage. We have experienced patients with ischemic vascular foot disease and combined skin ulceration and varing degree of soft tissue defect. In three patient with major vessel obstruction, we could preserve limb and avoid major amputation using greater saphenous vein graft with or without microvascular free tissue transfer.
Amputation
;
Extremities
;
Foot Diseases
;
Foot*
;
Humans
;
Limb Salvage
;
Osteomyelitis
;
Saphenous Vein
;
Skin Ulcer
;
Transplants
;
Vascular Diseases
;
Veins
10.Anesthetic Management for Thoraco-Xiphopagus Conjoined Twins: A case report.
Sang Do HAN ; Seong Hyun YANG ; Sung Su CHUNG ; Chang Young JEONG ; Chan Jin PARK
Korean Journal of Anesthesiology 1997;33(1):172-177
The incidence of conjoined twins is so rare that few anesthesiologists have an opportunity of managing them. Especially in Korea, there are only a few reports describing the anesthetic management for surgical separation of newborn conjoined twins. We experienced the successful anesthetic management for surgical separation of thoraco-xiphopagus conjoined twins without any particular problems. After applying the noninvasive monitors (ECG, pulse oximeter), one of the twins (twinA) with congenital heart disease was administered with intravenous ketamine for induction of anesthesia and intubated without neuromuscular blocker. Anesthesia was maintained with N2O-O2 and hand ventilation using Mapleson D breathing circuit. After maintaining airway of the twinA, the twinB was intubated and maintained with the same manner. Eighteen days after the separation procedure, the twinA with congenital heart disease died and the other one, twinB has been alive with normal growth and development.
Anesthesia
;
Growth and Development
;
Hand
;
Heart Defects, Congenital
;
Humans
;
Incidence
;
Infant, Newborn
;
Ketamine
;
Korea
;
Neuromuscular Blockade
;
Respiration
;
Twins, Conjoined*
;
Ventilation