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1.
Korean Journal of Dermatology ; : 295-297, 2000.
Article in Korean | WPRIM | ID: wpr-95535

ABSTRACT

Aplasia cutis congenita(ACC) is a rare congenital anomaly characterized by a well-demarcated skin defect. In the majority of cases it is limited to the scalp especially on the vertex although other areas of the body may also be involved. We report a case of aplasia cutis congenita, in a month-old female infant born with a round shaped hairless transparent menbrane on the left temporal area of the scalp. No associated other congenital anomalies were in this case.


Subject(s)
Female , Humans , Infant , Ectodermal Dysplasia , Scalp , Skin
2.
Korean Journal of Dermatology ; : 798-800, 1999.
Article in Korean | WPRIM | ID: wpr-96655

ABSTRACT

Lichen aureus is a variant of pigmented purpuric lichenoid dermatitis. The skin lesions usually appear asymptomatic rusty, copper, or orange colored roundish lichenoid erythematous-purpuric papules and patches on the lower extremities. Histologically, the epidermis shows minimal changes, with a dense lymphohistiocytic infiltrate observed in the superficial derrnis, typically distributed in a band-like fashion. The typical lesion is a single patch localized on the lower extremity. We report a rare case of segmental lichen aureus localized on the right lower extremity.


Subject(s)
Citrus sinensis , Copper , Dermatitis , Epidermis , Lichens , Lower Extremity , Skin
3.
Korean Journal of Dermatology ; : 544-546, 1999.
Article in Korean | WPRIM | ID: wpr-229249

ABSTRACT

Pigmented lesions of palmar and plantar skin may cause diagnostic problems, because some features of benign lesions in these sites may raise the suspicion of melanoma if considered alone. Transepidermal elimlnation is a mechanism by which a substance is eliminated through the epidermis, and it is apt to be confused with a feature of melanoma that tumor cells are located at all layers of the epidermis. We report a case of transepidermal elimination of nevus cells in acral letiginous nevus which needs a differential dignosis of melanoma.


Subject(s)
Epidermis , Melanoma , Nevus , Skin
4.
Korean Journal of Dermatology ; : 641-645, 1999.
Article in Korean | WPRIM | ID: wpr-158381

ABSTRACT

Mycosis fungoides(MF) is a cutaneous T-cell lymphoma of low-grade malignancy characterized by the proliferation of small to medium-sized cerebriform lymphoid cells confined to the skin. It usually shows favorable prognosis, but morphologic transformation occurs in some cases and is often associated with a more aggressive clinical course. Herein we report a case of Ki-1 positive large cell lyrnphoma (Ki-1 LCL) which developed in the plaque stage of mycosis fungoides. Although the lesions responded well to low-dose methotrexate therapy and there was no evidence of local or systemic recurrence until now, continuous follow-up is needed because the prognosis of transformed MF is known to be poor compared with primary cutaneous Ki-1 LCL. We also discussed the differential diagnosis of primary cutaneous Ki-1 positive lymphoproliferative disorders.


Subject(s)
Diagnosis, Differential , Follow-Up Studies , Lymphocytes , Lymphoma , Lymphoma, T-Cell, Cutaneous , Lymphoproliferative Disorders , Methotrexate , Mycosis Fungoides , Prognosis , Recurrence , Skin
5.
Annals of Dermatology ; : 97-100, 1998.
Article in English | WPRIM | ID: wpr-181930

ABSTRACT

We report a case of pulmonary infarction probably related with Henoch-Schönlein purpura, which presented with purpura on both lower extremities in a 27-year-old woman. The purpura had developed 4 days previously and it had no itching or tend'erness. She complained of mild fatigue, chest tightness, but no dyspnea or hemoptysis. On routine examination, chest radiography showed a poorly defined nodular opacity on the left lung field, and it was diagnosed by a follow up chest CT as a pulmonary infarction secondary to pulmonary vasculitis.


Subject(s)
Adult , Female , Humans , Dyspnea , Fatigue , Follow-Up Studies , Hemoptysis , Lower Extremity , Lung , Pruritus , Pulmonary Infarction , Purpura , Radiography , Thorax , Tomography, X-Ray Computed , Vasculitis
6.
Korean Journal of Dermatology ; : 372-375, 1998.
Article in Korean | WPRIM | ID: wpr-219453

ABSTRACT

Trichoadenoma is a rare cutaneous tumor that was first described by Nikolowski in 1958. It usually occurs as a single tumor on the face and its size varies from 3 to 50mm in diameter. It may arise any time during adult life. This tumor is less mature than trichofolliculoma and more differentiated than trichoepithelioma, and it is considered as a benign tumor with differentiation toward the infundibular portion of the pilosebaceous canal. In this report, we describe a 61-year-old women who developed trichoadenoma on the left shoulder of 3 years duration. The lesion was asymptomatic and had grown slowly. Histopathological findings showed numurous horn cysts with central keratinous material and solid tumor islands reaching to the deep dermis. Immunohistochemical studies showed negative findings for eccrine differentiation.


Subject(s)
Adult , Animals , Female , Humans , Middle Aged , Dermis , Horns , Islands , Shoulder
7.
Korean Journal of Dermatology ; : 914-917, 1998.
Article in Korean | WPRIM | ID: wpr-60958

ABSTRACT

Most insects including the honeybee cause erythema and edema at the site of a sting in non-allergic individuals. This reaction usually resolves within a few days. However, in certain cases, the persistence of inciting materials in the cutaneous tissue may promote a local inflammatory foreign body reaction. Localized nodular lesions were seen in our two patients and erythemstous patches were present in one patient due to rarely encountered complications induced by retained sting materials. In these cases histopathology showed multiple foci of foreign body granuloma containing yellow refraetile material in the center surrounded by histiocytes and foreign body giant cells. The granulomatous skin lesions in these patients were treated with intralesional injections of triamcinolone acetonide and partial excisions of the nodular masses were performed.


Subject(s)
Humans , Bites and Stings , Edema , Erythema , Foreign-Body Reaction , Giant Cells, Foreign-Body , Granuloma , Granuloma, Foreign-Body , Histiocytes , Injections, Intralesional , Insecta , Skin , Triamcinolone Acetonide
8.
Korean Journal of Medical Mycology ; : 24-32, 1998.
Article in Korean | WPRIM | ID: wpr-24237

ABSTRACT

BACKGROUND: Steroid acne is a folliculitis that can result from a systemic or topical administration of steroid and has been described as showing similar clinical pictures to Malassezia folliculitis, but there have been few reports about the incidence of Malassezia in steroid acne and other acneiform eruptions. OBJECTIVE: Our purpose was to describe the incidences of Malassezia in acneiform eruptions and to discuss about the relationship between clinical steroid acne and Malassezia folliculitis. METHODS: The history, clinical features, direct microscopy, histopathological analysis, and therapeutic results of 125 cases with steroid acne or other acneiform eruptions were described and compared. RESULTS: Over 80% of patients with acneiform eruption receiving systemic steroid revealed significant numbers of Malassezia in the lesional follicle. CONCLUSION: Steroid acne and other acneiform eruptions showing discrete follicular papules and/or pustules localized to the upper trunk or acneiform facial skin lesions associated with multiple acneiform lesions on the body in the summer period should be suspected as Malassezia folliculitis.


Subject(s)
Humans , Acne Vulgaris , Acneiform Eruptions , Administration, Topical , Folliculitis , Incidence , Malassezia , Microscopy , Skin
9.
Annals of Dermatology ; : 159-162, 1998.
Article in English | WPRIM | ID: wpr-49668

ABSTRACT

We describe the case of a 45-year-old woman who had self-regressing livedo reticularis on the lower extremities. Examination of a biopsy specimen from the mottled area revealed myxomatous emboli in the deep dermal arterioles. Echocardiography showed a myxoma in the left atrium. After the tumor was surgically excised, the patient had no further evidence of the disorders during the 3-year period of follow-up. Livedo reticularis caused by an peripheral arterial embolism, which in turn was caused by the tumor fragments in our patient with left atrial myxoma, is considered to be unusual.


Subject(s)
Female , Humans , Middle Aged , Arterioles , Biopsy , Echocardiography , Embolism , Follow-Up Studies , Heart Atria , Livedo Reticularis , Lower Extremity , Myxoma
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