1.ARTERIALIZED VENOUS FLAP FOR COVERAGE OF MULTIPLE DIGITAL DEFECTS OF THE HAND.
Young Gyun CHOI ; Jeung Joon PARK
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1997;24(4):766-774
No abstract available.
Hand*
2.A Case of Lymphomatoid Papulosis Treated with PUVA.
Kea Jeung KIM ; Hyang Joon PARK ; Tae Young YOUN ; Yoo Shin LEE
Korean Journal of Dermatology 1983;21(3):351-355
Lymphomatoid papulosis is a disease; clinically benign, histologically malignant. Clinically, it may sirnulate pityriasis lichenoides et varioliformis acuta, but histologically it suggest malignant lympboma due to the presence of polymorphous lymphoid infiltrate consisting of sma11 lymphocytes intermingled with conspicuous large atypical cells. Recently, many autbors consider lymphornatoid papulcsis as a Cutaneous T-cell lymphoma, and malignancy has been reported to develop in some patients. We experienced a case of lyrnphomatoid papulosis in 26-year-old woman and treated with PUVA successfully. PUVA treatment may be proven useful in controlling this disease and it rnay also inhibit the development of malignancy.
Adult
;
Female
;
Humans
;
Lymphocytes
;
Lymphoma, T-Cell, Cutaneous
;
Lymphomatoid Papulosis*
;
Pityriasis Lichenoides
3.Two Cases of Generalized Pustular Psoriasis in Brother and Sister.
Kea Jeung KIM ; Hyang Joon PARK ; Gwang Yeol JOE ; Yoo Shin LEE
Korean Journal of Dermatology 1983;21(3):345-349
Generalized pustular psoriasis which is originally described by von Zumbusch in 1910, is the most intense form of the acute exanthematic variant among psoriasis. It is to be occured as a rare disease and the familial occurrence rarely has been reported. Many therapeutic attempts have been rnade to bring the condition under control, but none has unequivocally proven to alter its courae decisively. We present two cases of generalized pustular psoriasis in brother and sister (16 year-old male, 19 year-old female) which were treated successfully by pbotochemotherapy (PUVA).
Humans
;
Male
;
Psoriasis*
;
Rare Diseases
;
Siblings*
;
Young Adult
4.Two Cases of Eruptive Vellus Hair Cysts.
Hyang Joon PARK ; Seon Hoon KIM ; Jeung Hoon LEE ; Yoo Shin LEE
Korean Journal of Dermatology 1984;22(3):330-333
We present two oases of Eruptive Vellus Hair Cysts(EVHC) in 30- year-old and 27- year old women. They had 6 to 10 discrete, asymptomatic, brown or reddish brown papules on the neck, axilla, chest and extremities. The clinical impressions were epidermal cyst and steatocystoma multiplex espectively, but histopathological exarnination revealed smal1 cysts in middermis containing numerous vellus hairs cut transversely or obliquely and surrounding granulomatous foreign body reaction typical to EVHC. Transepithelial elimination was not found.
Axilla
;
Epidermal Cyst
;
Extremities
;
Female
;
Foreign-Body Reaction
;
Hair*
;
Humans
;
Neck
;
Steatocystoma Multiplex
;
Thorax
5.Lectin-binding patterns by ABO blood grouping in human nasal mucosa.
Jeung Gweon LEE ; Joo Heon YOON ; In Yong PARK ; Il Joon OH
Korean Journal of Otolaryngology - Head and Neck Surgery 1992;35(3):387-394
No abstract available.
Blood Grouping and Crossmatching*
;
Humans*
;
Nasal Mucosa*
6.Arteriovenous Hemangioma Developed after Fine Needle Biopsy of Thyroid.
Seung Bae PARK ; Eun Hwa LIM ; Myung IM ; Young LEE ; Jeung Hoon LEE ; Young Joon SEO
Korean Journal of Dermatology 2013;51(6):435-437
Fine needle biopsy of nodules on the thyroid is simple diagnostic method and it is generally a safe procedure. The main side effect is pain and hematoma. Secondary hemangioma development after biopsy is extremely rare. A 63-year-old woman presented with a 5-year history of solitary erythematous papule on neck. Spontaneous bleeding recorded six times within 5 years. There is not vascular anastomosis in ultrasonographic imaging. A histopathologic study showed vessel-like arteriole around small veins in dermis. No arteriovenous hemangioma case has been previously reported to be related to fine needle biopsy. Our case showed possibilities of arteriovenous hemangioma developments after fine needle biopsy.
Arterioles
;
Biopsy
;
Biopsy, Fine-Needle
;
Dermis
;
Female
;
Hemangioma
;
Hematoma
;
Hemorrhage
;
Humans
;
Neck
;
Thyroid Gland
;
Veins
7.A Case of Plaque-type Blue Nevus.
Young LEE ; Kyung Chae KYE ; Jeung Hoon LEE ; Jang Kyu PARK ; Young Joon SEO
Korean Journal of Dermatology 2006;44(2):232-234
Blue nevi are usually solitary, but they may be multiple and form a plaque composed of multiple papules or nodules with an intervening flat area of blue coloration. It looks like a benign and asymptomatic lesion. However, because of its rarity, no definitive prognosis can be given. An 18-year-old male presented with a 5 x 4 cm-sized, speckled blue-black tumor on his posterior neck, which had existed since birth. Histopathologic examination showed clumps of melanocytes intermingled with irregularly arranged collagen bundles in the mid and lower dermis, with some extending to the subcutaneous tissue. We diagnosed the lesion as a plaque-type blue nevus, based on histopathologic findings of common blue nevus.
Adolescent
;
Collagen
;
Dermis
;
Humans
;
Male
;
Melanocytes
;
Neck
;
Nevus, Blue*
;
Parturition
;
Prognosis
;
Subcutaneous Tissue
8.A Case of Giant Basal Cell Carcinoma.
Yong Hee NAM ; Bo Joong KIM ; Young Joon SEO ; Jeung Hoon LEE ; Jang Kyu PARK
Korean Journal of Dermatology 2006;44(2):224-226
Basal cell carcinoma (BCC) represents the most common cutaneous malignancy in caucasions. Most of the tumors usually occur on sun-exposed skin, and they are small and easily treated. Giant BCC is a rare variant of this tumor and is defined as a lesion greater than 5 cm at its largest diameter. For the development of giant BCC, several risk factors, including patient neglect, aggressive histological features and long duration, have been identified. We observed a very large BCC on the face and scalp of an elderly woman. She had been reclusive for a long time, and this problem might have played a crucial role in the development of the giant BCC.
Aged
;
Carcinoma, Basal Cell*
;
Female
;
Humans
;
Risk Factors
;
Scalp
;
Skin
9.A Case of Churg-Strauss Syndrome Showing Severe Skin Necrosis.
Myung IM ; Yong Hee NAM ; Young Joon SEO ; Jeung Hoon LEE ; Jang Kyu PARK
Korean Journal of Dermatology 2006;44(2):216-219
Churg-Strauss syndrome is a disorder characterized by asthma, fever, systemic vasculitis, extravascular granulomas and hypereosinophilia. A 70-year-old woman with a 2-year history of bronchial asthma was admitted to hospital, due to extensive hemorrhagic bullae embedded in necrotic tissue on both extremities, the buttocks and trunk. The patient showed abnormal laboratory findings including significant peripheral blood eosinophilia and p-ANCA (+), and histopathologically leukocytoclastic vasculitits with marked eosinophlilic infiltration. Based on the clinical course, laboratory data and pathologic findings, the diagnosis of Churg-Strauss syndrome was made. Treatment with oral prednisolone was started, and the clinical findings improved.
Aged
;
Antibodies, Antineutrophil Cytoplasmic
;
Asthma
;
Buttocks
;
Churg-Strauss Syndrome*
;
Diagnosis
;
Eosinophilia
;
Extremities
;
Female
;
Fever
;
Granuloma
;
Humans
;
Necrosis*
;
Prednisolone
;
Skin*
;
Systemic Vasculitis
10.A Case of Poroma with Features of Hidroacanthoma Simplex and Dermal Duct Tumor.
Yong Hee NAM ; Young Joon SEO ; Jeung Hoon LEE ; Jang Kyu PARK ; Ji Seog YOON
Korean Journal of Dermatology 2006;44(1):120-123
Hidroacanthoma simplex, eccrine poroma and dermal duct tumors have recently come to be viewed as variants of benign poroid neoplasia, due to their similar histopathologic and cytologic features. Some authors have reported the association of two or three of these tumors in a single lesion. We herein report a patient with two subtypes of poroma in a single lesion.
Humans
;
Poroma*