1.A Case of Malignant Pyoderma.
Jee Ho CHOI ; Jai Il YOUN ; Yoo Shin LEE
Korean Journal of Dermatology 1984;22(4):413-417
Malignant pyoperma is a rare, chronic, progressive, destructive ulcerating skin disease of unknown cause that affects the head and neck region of young adults. The disease is progressive but responds to high doses of systemically administered steroids. We present a case of malignant pyoderma developed on the left retroauricular area in 67 year-old male. The patient died of rapidly progressive, desructive, 15cm x 20 cm sized, phagedenic ulcer on the left retroauricular and neck area despite of various extensive local and systemic treatment. Histopathologic findings of tissue from the edge of the ulcer were non-specific, showing upper dermal necrosis and mixed inflammatory cell infiltrate in the deep dermis.
Aged
;
Dermis
;
Head
;
Humans
;
Male
;
Neck
;
Necrosis
;
Pyoderma*
;
Skin Diseases
;
Steroids
;
Ulcer
;
Young Adult
2.Reconstruction of the foot by first web space island flap.
Hyun Ho KIM ; Byung Il PARK ; Jai Koo CHOI
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(2):273-280
No abstract available.
Foot*
3.Immunohistochemical study on sweat gland tumors with monoclonal antibodies against S-100 subunits.
Kyung Jeh SUNG ; Kwang Hyun CHO ; Ho Seok SUH ; Jee Ho CHOI ; Jai Kyoung KOH
Korean Journal of Dermatology 1992;30(4):446-453
S-100 protein is a mixture of three proteins, that is, S-100 ao(aa), S-100 a(ab) and, S- 100 b(bb). Twenty-two case, of sweat gland tumors were stained with immunoperoxidase technique (ABC method) for the presence of S-100a and b-subunit. Four syringomas, four eccrine poromas, two eccrine porocarcinomas, two ecerine spirdeiomas, one papillary eccrine adenoma, three clear cell hidradenomas, three mixed tumr rs of the skin, two papillary syringocystadenomas, and one cylindroma were included. All specimens were formalin-fixed and paraffin-embedded. The results were as follows : 1) The staining patterns of anti-S-100a and b-protein antibodies we e simillar to those of anti-S-100 protein antibody except in eccrine poroma and porocare nomal. 2) In eccrine poroma and porocarcinoma, scattered S-100-positive dendritic cells within tumor cell nests were stained by S-100-protein antibody (3/6), but not by anti-S-100a protein antibody. S-100p is present in normal Langerhans cells. Therefore this finding suggests that these cells niay be Langerhans cells
Acrospiroma
;
Adenoma
;
Antibodies
;
Antibodies, Monoclonal*
;
Carcinoma, Adenoid Cystic
;
Dendritic Cells
;
Eccrine Porocarcinoma
;
Immunoenzyme Techniques
;
Langerhans Cells
;
Poroma
;
S100 Proteins
;
Skin
;
Sweat Glands*
;
Sweat*
;
Syringoma
4.A Case of Trichoblastic Fibroma.
Hwa Jung LEE ; Dong Jin IM ; Ho Seok SUH ; Jee Ho CHOI ; Jai Kyoung KOH
Annals of Dermatology 1996;8(4):265-268
Trichogenic tumors are very rare and described as cutaneous neoplasms probably derived from hair germ which develops into hair follicles. We report a case of trichoblastic fibroma on the left parietal scalp of a 45-year-old man. The lesion was a solitary, firm, non-tender, 2×2cm subcutaneous nodule. The histopathological study showed a well circumscribed dermal tumor composed of abundant basophilic palisading basaloid lobules with some keratinous cysts, hair follicle differentiation and fibroblastic stroma.
Basophils
;
Fibroblasts
;
Fibroma*
;
Hair
;
Hair Follicle
;
Humans
;
Middle Aged
;
Rabeprazole
;
Scalp
5.An Immunohistochemical Study of Molluscum Contagiosum.
Ho Seok SUH ; Jee Ho CHOI ; Kyung Jeh SUNG ; Jai Kyoung KOH
Korean Journal of Dermatology 1994;32(5):787-794
BACKGROUND: Molluscum contagiosum is a common viral infect oudisease of the skin and mucous membrane that is caused by a molluscum contagiosum virus(MCV; which belongs to the poxviridae family. One of the characteristic histopathologic findings is an epidermal hyperplasia Porter and Archard reported that this phenomenon might be explained by a virus induced epidermal growth factor (EGF) like polypeptide. There was a report that epidermal prolifeation in viral infection might be modulated by other factors than the virus itself such as local immune response. OBJECTIVE: The purpose of this study was to examine the expression pattern of epidermal growth factor receptor and other immunocompetent cells by immunohistochemical stainings. METHOD : We performed iinmunoperoxidase staining on the 11 slaecmens of formalin-fixed, paraffin-embedded molluscum lesions and 15 specimens of snap frozen mollucum lesions with nine primary antibodies(EGFR, factor XIIIa, CDla, S-100 protein, MAC 387, HLA-IR, CD4, CDS, L26) RESULTS: EGF receptors were strongly expressed in lesional MCV ifect,ed keratinocytes. The number of CDla and factor XIIIa positive dermal dendritic cells were sigtly increased. In inflamed lesions, CD4 and HLA-DR expressions were increased in the dermis and per lesional epidermis. CONCLUSION: This study shows that 1) increased EGFR expression is of MCV infected keratinocytes may be related to the pathogenesis of epidermal hyperplasia. 2) helper T lyrnphocytes may operate in inflamed molluscum lesions.
Dermis
;
Epidermal Growth Factor
;
Epidermis
;
Factor XIIIa
;
HLA-DR Antigens
;
Humans
;
Hyperplasia
;
Keratinocytes
;
Langerhans Cells
;
Molluscum Contagiosum*
;
Mucous Membrane
;
Poxviridae
;
Receptor, Epidermal Growth Factor
;
S100 Proteins
;
Skin
6.Three Cases of Neutrophilic Eccrine Hidradenitis.
Ho Seok SUH ; Moon Soo YOON ; Jee Ho CHOI ; Kyung Jeh SUNG ; Jai Kyoung KOH
Annals of Dermatology 1995;7(2):200-205
Neutrophilic eccrine hidradenitis(NEH) was originally described in 1982 by Harrist et al. in a patient with myelogenous leukemia receiving chemotherapy. Clinically NEH represents various cutaneous manifestations with or without tenderness and pruritus. Histologic examination demonstrates a neutrophilic infiltrate within and around the eccrine gland and degeneration of the eccrine gland structures. Although the pathogenesis and possible cause of NEH remain unknown, it is probably an unusual cutaneous reaction to chemotherapeutic agents. A few cases of infection associated eccrine hidradenitis are found in the literature. We report three cases of neutrophilic eccrine hidradenitis. Two cases were associated with hematologic malignancy. The third case was associated with an infection of Vibrio vulnificus.
Drug Therapy
;
Eccrine Glands
;
Hematologic Neoplasms
;
Hidradenitis*
;
Humans
;
Leukemia, Myeloid
;
Neutrophils*
;
Pruritus
;
Vibrio vulnificus
7.A Case of Acquired Digital Fibrokeratoma: Immunohistochemical Stain with Anti - factor XIIIa antibody.
Ho Seok SUH ; byung Jick RYU ; Jee Ho CHOI ; Kyung Jeh SUNG ; Jai Kyoung KOH
Korean Journal of Dermatology 1994;32(6):1131-1135
In normal hurnan dermis, factor XIIIa positive dermal dendrocyte are located in the papillary areas closely associated with blood vessels and the upper reticular dem These cells represent a specific type of bone marrow derived dermal cells, distinct from Langerhans cells having some features in common with rnonocyte/macrophage lineage and with potential antier presenting activity. Although the significance of these cells has not yet been fully established, it been suggested that they play a major role in skin immune iesponses, in collagen synsthesis regultic and in wound repair. We report a case of acaqired fibrokeratoma which is studiec conventional histopathology and immunohistochemistry. Histopathologic findings of this case showed ovascular proliferation and the increased presence of fibroblast like cells as a common fe;ture of these benign tumors. Immunohistochemical staining with anti factor XIIIa antibody deiaoi strates increased numbera of positive dendritic cells in the upper dermis. There finding supports the fat that some fibroblagt like cells in the upper dermis of acquireid fibrokeratoma may be factor XIIIa positive dermal dendritic cells.
Blood Vessels
;
Bone Marrow
;
Collagen
;
Dendritic Cells
;
Dermis
;
Factor XIIIa*
;
Fibroblasts
;
Immunohistochemistry
;
Langerhans Cells
;
Skin
;
Wounds and Injuries
8.A Case of Winkelmann Granuloma.
Kyoung Ae JANG ; Jee Ho CHOI ; Kyung Jeh SUNG ; Kee Chan MOON ; Jai Kyoung KOH
Annals of Dermatology 1998;10(3):163-166
We report a case of Winkelmann granuloma in a 63-year-old man. nstopathological findings of the biopsy specimens from the lesions of the ear, finger and iliac crest area were compatible with Winkelmann granuloma. Winkelmann granuloma is a rare disorder showing an association with systemic immunoreactive disorders. Although our patient did not have any definite systemic disease, he had characteristic clinical and histopathological findings of Winkelmann granuloma, arthralgia, an elevated erythrocyte sedimentation rate, positivity to the rheumatoid factor and antinuclear antibodies. Therefore, we believed that he was strongly suspected to have an unclassifiable systemic immunoreactive disease.
Antibodies, Antinuclear
;
Arthralgia
;
Biopsy
;
Blood Sedimentation
;
Ear
;
Fingers
;
Granuloma*
;
Humans
;
Middle Aged
;
Rheumatoid Factor
9.A Case of Accessory Auricles on the Left Preauricular and Left Buccal Areas.
Jee Ho CHOI ; Joon Mo YANG ; Jai Il YOUN ; Yoo Shin LEE
Korean Journal of Dermatology 1983;21(4):457-460
Accessory auricle is a relatively rare congenital anomaly arised from the abnormaI development of the auricular tubercles or from the tissues surrounding the second, third and fourth branchial clefts. Clinically this anomaly is a small akin-colored tag or nodule, soft and globular or cartilaginous consistency on or near the tragus along a line drawn from the tragus to the angle of the mouth or along the anterior margin of the sternomastoid muscle. The lesion is usually solitary and located in the preauricular area but may be multiple and rarely bilateral. We present a typical caae of accessory auricles in 4-day-old female infant. The patient had two skin-colored firm nodules on the left preauricular area and well pedunculated one on the Ieft buccal area near the angle of the rnouth. Histopathologic find.ings showed numerous pilosebaceous units, abundant subcutaneous fat and cartilage tissue in the center of the lesion.
Branchial Region
;
Cartilage
;
Female
;
Humans
;
Infant
;
Mouth
;
Subcutaneous Fat
10.Substance P and VIP = induced Flare and Wheal Responses in Normal Healthy Persons.
byung Jick RYU ; Jee Ho CHOI ; Jai Kyoung KOH ; Kyung Jeh SUNG
Korean Journal of Dermatology 1995;33(3):497-503
BACKGROUND: Despite concern about information of neuropeptide, the has been no baseline study of neuropeptide in Koreans. OBJECTIVE: The purpose of the study was to investigate the skin sinsitivity of substance P and VIP in normal healthy persoas. METHODS: We prepared 1000pM, 100pM, 10pM solution of substan P 1-11, substnace P 1-7, substnace P 7-11, and VIP. We injected intradermally 50ul of the br ve solutions on 12 sites of both forearms in addition plaebo. We measured the size of the area of flare and wheal along time. We repeated the same test after antihistamine intake. RESULTS: Flare and wheal respinses were dose dependent. Injection of substance P 1-7 did not evoke wheal responses and injection of substance P 7-11 did not wake flare responses. Flare responses of substance P 1-11, ubstance P 7-11, VIP were inhibiteb antihistamine and wheal responses of VIP were inhibitedly antihistamine. CONCLUSION: N-terminal of subtance P is responsible for flarers onses and C-terminal of substnace P is responsible for wieal responses. Flare responses of sisance P were mediated by histamine but wheal responses osubstance P were direct effect on postcapillary venule. Flare and wheal responses of VIF were mediated by histamine.
Forearm
;
Histamine
;
Humans
;
Neuropeptides
;
Skin
;
Substance P*
;
Venules