1.Reconstruction of a lateral collateral ligament of the proximal interphalangeal joint of the fingers.
Kwang Sik KOOK ; Min Nieng LEE ; Sang Hun HAN
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1991;18(6):1153-1160
No abstract available.
Fingers*
;
Joints*
;
Lateral Ligament, Ankle*
2.A Case of Intravenous Pyogenic Granuloma of the Palm.
June Young CHOI ; Kwang Soo HAN ; Hyung Geun MIN ; Jong Min KIM
Annals of Dermatology 2000;12(3):222-224
Intravenous pyogenic granuloma (IVPG) is a form of pyogenic granuloma (PG) in which the capillary proliferation is confined entirely within the lumen of a vein. It occurs typically in the neck and upper extremities. Histologically, this benign lesion is similar to PG of other localizations and is characterized by a lobular proliferation of capillaries growing in a sparsely cellular, edematous collagenous stroma. We report a case of IVPG developing in the palm, an unusual site of occurrence.
Capillaries
;
Collagen
;
Granuloma, Pyogenic*
;
Neck
;
Upper Extremity
;
Veins
3.Biopsy Induced Acquired Digital Fibrokeratoma.
Min Seok KIM ; Han Su KIM ; Eun Byul CHO ; Eun Joo PARK ; Kwang Ho KIM ; Kwang Joong KIM
Korean Journal of Dermatology 2014;52(11):835-836
No abstract available.
Biopsy*
4.A Case of Renal Cell Carcinoma Metastatic to the Scalp.
June Young CHOI ; Kwang Soo HAN ; Hyung Don BANG ; Kwang Ho KIM ; Kwang Joong KIM ; Jong Min KIM
Korean Journal of Dermatology 2001;39(6):711-713
Cutaneous metastasis from renal cell carcinoma is unusual and have been reported infrequently. We report a case of metastatic renal cell carcinoma in a 33-year-old man who presented with a 3.5X2.0 cm-sized round, brightly red colored nodule on the scalp for 1 month. A skin biopsy revealed the typical clear cell adenocarcinoma with clear cytoplasm and oval hyperchromatic nuclei arranged in glandular pattern consistent with metastatic renal cell carcinoma. In most instances, once cutaneous involvement is manifested the disease is widespread and has a poor prognosis. But, our case presented only a single cutaneous nodule, and workup showed no evidence of further metastasis for 1 year.
Adenocarcinoma, Clear Cell
;
Adult
;
Biopsy
;
Carcinoma, Renal Cell*
;
Cytoplasm
;
Humans
;
Neoplasm Metastasis
;
Prognosis
;
Scalp*
;
Skin
5.A Case of Lupus Erythematosus Panniculitis with Infiltration of Atypical Lymphocytes.
Sung Ju PARK ; Kwang Soo HAN ; Ho Gyun LEE ; Jong Min KIM
Korean Journal of Dermatology 1998;36(6):1074-1077
Lupus erythematosus panniculitis is a rare variant of lupus erythematosus primarily involving a panniculus with or without discoid lupus erythematosus in the overlying skin. A 34-year-old woman showed multiple, variable-sized, indurated subcutaneous nodules on both her upper arms and axillae. A Histopathological examination revealed lobular panniculitis with infiltration of several hyperchromatic atypical large lymphocytes. The infiltrated cells were positively stained with LCA, UCHL-1, CD4, CD8, but not with CD20 and CD68. A T cell receptor -chain gene and immunoglobulin heavy chain gene rearrangement study showed no monoclonality. The result of an ANA test was positive at 1: 40 in a homogeneous pattern. Skin lesions were improved by combined therapy with daily hydroxychloroquine 400mg and prednisolone 10mg in a week and after 6weeks, resolved with atrophic depressed scars. After 4 months, she complained of symptoms of the Raynaud phenomenon and was managed by nifedipine. There has been no recurrence during follow-up for 7 months.
Adult
;
Arm
;
Axilla
;
Cicatrix
;
Female
;
Follow-Up Studies
;
Gene Rearrangement
;
Humans
;
Hydroxychloroquine
;
Immunoglobulin Heavy Chains
;
Lupus Erythematosus, Discoid
;
Lymphocytes*
;
Nifedipine
;
Panniculitis
;
Panniculitis, Lupus Erythematosus*
;
Prednisolone
;
Raynaud Disease
;
Receptors, Antigen, T-Cell
;
Recurrence
;
Skin
6.Three cases of atypical Kawasaki disease with coronary aneurysm.
Min Young PARK ; Kwang Sun HAN ; Sung Yoon CHO ; Byoung Soo CHO ; Sung Ho CHA
Journal of the Korean Pediatric Society 1993;36(9):1315-1319
Kawasaki disease is described by fever lasting five days or more, bilateral conjunctival injection, changes of lips and oral cavity, polymorphous exanthema, acute non-purulent cervical lymphadenopathy, and changes of extremities. Atypical Kawasaki disease is defined as fewer than 4 of 6 criteria described above including coronary artery abnormalities. Especially, atypical clinical manifestations of Kawasaki disease appear in infants younger than 6 months old of age. Thus we recommend echocardiography in early infancy who has prolonged fever in order to diagnose atypical Kawasaki disease and treat early. We have experienced three cases of atypical Kawasaki disease with coronary aneurysm who were admitted because of fever and revealed coronary aneurysm on echocardiography.
Coronary Aneurysm*
;
Coronary Vessels
;
Echocardiography
;
Exanthema
;
Extremities
;
Fever
;
Humans
;
Infant
;
Lip
;
Lymphatic Diseases
;
Mouth
;
Mucocutaneous Lymph Node Syndrome*
7.Urinary Stone in Childen.
Sang Won HAN ; Young Min EUN ; Kwang Sik RHO ; Pyung Kil KIM
Journal of the Korean Society of Pediatric Nephrology 1997;1(1):60-66
Herpes simplex virus type 1 and 2 (HSV-1, HSV-2) are the ubiquitous human pathogens responsible for a variety of afflictions. HSV-2 is one of the viruses that were suspected of promoting carcinogenesis in the uterine cervix. Certainly, there is a need for the more sensitive and accurate laboratory techniques for HSV detection. We examined total 80 cases of smears including 17 Tzanck smears of skin and 63 cases of Papanicolaou smears from total 77 patients with clinical impression of herpetic infections, from September, 1985 through August, 1989. Immunohistochemical typings for HSV-1 and HSV-2 were performed together with routine cytologic findings and compared. The results are as follows ; 1) Patients were 9 males and 33 females, and age distribution was between 5 and 71 years 2) Subjective symptoms such as ulceration, vesicle, vaginal discharge, pruritus, and pain were complained in 36 patients and 38 cases were genital herpes. Recurrence was noted in 11 cases. 3) Positive results were obtained in 42 among 80 cases. 4) Both routine cytology and immunohistochemical staining were positive in 13 cases and in 24 cases only immunohistochemical staining were positive. 5 cases were positive only in routine cytologic smears. 5) The cases that immunocytochemical stain had been performed were 37 cases, which were all positive in type 2. Among the above 37 cases, type 1 also were positive in 5 cases. The results show that the immunoperoxidase technique is one of the rapid and reliable method to confirm the herpetic when suspected and that it is particularly useful when the Papanicolaou smear findings are equivocal.
Age Distribution
;
Carcinogenesis
;
Cervix Uteri
;
Female
;
Herpes Genitalis
;
Herpesvirus 1, Human
;
Herpesvirus 2, Human
;
Humans
;
Immunoenzyme Techniques
;
Male
;
Papanicolaou Test
;
Pruritus
;
Recurrence
;
Skin
;
Ulcer
;
Urinary Calculi*
;
Vaginal Discharge
8.A Case of Nerve Cheath Myxoma.
Kwang Soo HAN ; Jong Hun SHIN ; Ho Gyun LEE ; Jong Min KIM
Korean Journal of Dermatology 2000;38(5):694-697
No Abstract Available.
Myxoma*
9.A Case of Pearly Penile Papules.
Jong Hoon SHIN ; Kwang Soo HAN ; Ho Gyun LEE ; Jong Min KIM
Korean Journal of Dermatology 1998;36(6):1122-1124
Pearly penile papules are small, smooth, dome-shaped, grayish to skin-colored papules, that are arranged in one or several rows. These are commonly located circumferentially on the corona and sulcus of the glans penis. A 36-year-old male patient had had asymptomatic numerous pearly smooth 1 * 1mm -sized dome-shaped papules for several months. A Histopathological examination revealed an increased number of fibroblasts on the papillary dermis, vascular proliferation and a mild lymphocytic infiltration. We diagnosed the condition as pearly penile papules. No treatment other than reassurance was given. We report, herein, a case of pearly penile papules.
Adult
;
Dermis
;
Fibroblasts
;
Humans
;
Male
;
Penis
10.Intraosseous Epidermal Cyst of the Distal Phalanx: A Case Report.
Gyu Min KONG ; Joo Yong KIM ; Jung Han KIM ; Dae Hyun PARK ; Kwang Hun AN
The Journal of the Korean Bone and Joint Tumor Society 2014;20(1):22-26
An intraosseous epidermal cyst is a rare benign cystic lesion. It is thought to result from congenital factors or trauma and can lead to bone destruction because the cyst develops at the soft tissue around the bone. Radiological findings of intraosseous epidermal cysts are a well-defined radiolucent lesion, with cortical expansion. It is important to differentiate an intraosseous epidermal cyst with other disease developed at distal phalanx because its clinical and radiological findings are similar. We report two rare cases of intraosseous epidermal cysts that developed at the distal phalanx.
Epidermal Cyst*