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1.
Korean Journal of Dermatology ; : 423-427, 2002.
Artigo em Coreano | WPRIM | ID: wpr-99277

RESUMO

A nine year old boy presented asymptomatic multiple papular lesions for 6 months. Biopsy revealed typical features of xanthogranuloma with Touton type giant cells. Authors observed natural course of the lesions for about 2 years thereafter, which showed shrinkage of the existing papules in general in spite of newly appearing lesions. Review of the previous cases reported by the name of juvenile xanthogranuloma showed that the age of the onset of the most of the cases with multiple lesions was before one year after birth, but adolescent cases were rare. It was also noted that previous cases with such multiple lesions had a course of spontaneous regression regardless of the onset of its age.


Assuntos
Adolescente , Humanos , Masculino , Biópsia , Células Gigantes , Parto , Xantogranuloma Juvenil
2.
Korean Journal of Dermatology ; : 1379-1383, 2002.
Artigo em Coreano | WPRIM | ID: wpr-83565

RESUMO

Nevus sebaceus is a congenital cutaneous hamartoma which has a potential to develop both benign and malignant neoplasm in late life. The most common benign tumor developed within the nevus is syringocystadenoma papilliferum and the most common malignant tumor basal cell epithelioma. Although two different tumors often develop simultaneously on the lesion, it is rare to see more than two different tumors developing on the lesion of nevus sebaceus. In Korean literatures only three such cases were reported. We report an additional case of nevus sebaceus developing three different tumors, syringocystadenoma papilliferum, sebaceous epithelioma, and basal cell carcinoma, in a 67-year-old female patient.


Assuntos
Idoso , Feminino , Humanos , Carcinoma , Carcinoma Basocelular , Hamartoma , Nevo
3.
Korean Journal of Dermatology ; : 153-157, 2002.
Artigo em Coreano | WPRIM | ID: wpr-85928

RESUMO

Diffuse alopecia due to occult syringoma of the scalp has rarely been reported but the authors of the cases presented different opinions about which one is the primary event between the two conditions and if the syringoma is true or a reactive ductal proliferation. We have found a case whose diffuse alopecia is believed to be due to true syringoma of the scalp. A 43-year old woman showed simultaneous and gradual development of diffuse alopecia and multiple papular elevations on the face and neck adjoining the frontal and temporal hair lines. Histopathology of the scalp and the facial papular elevations all revealed typical syringomatous infiltrations with epithelial comma-tails and sclerotic stroma. All of the clinicopathological findings supported that the diffuse alopecia of the patient was due to the occult syringoma of the scalp.


Assuntos
Adulto , Feminino , Humanos , Alopecia , Cabelo , Pescoço , Couro Cabeludo , Siringoma
4.
Annals of Dermatology ; : 200-203, 2002.
Artigo em Inglês | WPRIM | ID: wpr-27219

RESUMO

BACKGROUND: For the treatment of generalized vitiligo patients with oral PUVA, we can use two different methods; one is to treat the lesions while the whole body is exposed. Another one is to treat the lesions while only the lesions are exposed. PURPOSE: This study was performed to determine whether lesional and whole body exposure in oral PUVA for generalized vitiligo show any therapeutic differences in effectiveness. METHODS: The vitiligo lesions were distributed over the whole body skin of the subjects and the lesion area was less than 6% of the whole skin area. PUVA was done to the subjects more than 20 times after oral administration of psoralen. The patients were classified into two different groups. One is the lesional exposure group in which the patient exposed only the vitiligo lesion. The other is the whole body exposure group in which the patient exposed almost their whole body. RESULTS: Our results show that there is no statistical difference of the therapeutic effectiveness between the two methods. CONCLUSIONS: We recommend lesional treatment rather than whole body treatment to prevent the oral PUVA side effects.


Assuntos
Humanos , Administração Oral , Ficusina , Pele , Vitiligo
5.
Korean Journal of Dermatology ; : 891-895, 2001.
Artigo em Coreano | WPRIM | ID: wpr-203224

RESUMO

We report a case of a tick bite by Ixodes nipponensis found on the neck of a 75-year-old female. The tick was thought to be in the lesion for 10 days. Till now 31 cases of tick bites were reported in Korea including the present case. The review of the Korean cases revealed that the ratio of female/male was 1.3 : 1, its age distribution was from 1st to 8th decade, sites of the invasion were trunk, head and neck, extremities, and anogenital area in order of frequency. Its prevalent season was spring and summer and the most common species(17/31) was Ixodes nipponensis.


Assuntos
Idoso , Feminino , Humanos , Distribuição por Idade , Extremidades , Cabeça , Ixodes , Coreia (Geográfico) , Pescoço , Estações do Ano , Picadas de Carrapatos , Carrapatos
6.
Korean Journal of Dermatology ; : 803-807, 2001.
Artigo em Coreano | WPRIM | ID: wpr-204687

RESUMO

Merkel cell carcinoma is a rapidly growing malignant neuroendocrine tumor with a high rate of recurrence and metastasis for which wide excision is recommended. About 10 cases of spontaneous regression have been reported in the world. We report a case of Merkel cell carcinoma which showed spontaneous regression. The patient was a 68-year-old woman with a two-month history of a rapidly enlarging dusky red tumor on her right cheek. Microscopically, the tumor cells were uniform with round to oval shaped nucleus and scanty cytoplasm, and showed trabecular arrangement. Ultrastructually, dense core neurosecretory granules 100 to 200nm in diameter were found in the cytoplasm of tumor cells. As far as we know, this is the first case of the spontaneous regression of the tumor in the country.


Assuntos
Idoso , Feminino , Humanos , Carcinoma de Célula de Merkel , Bochecha , Citoplasma , Metástase Neoplásica , Tumores Neuroendócrinos , Recidiva
7.
Korean Journal of Dermatology ; : 1063-1065, 2001.
Artigo em Coreano | WPRIM | ID: wpr-64662

RESUMO

Sebaceous trichofolliculoma, which is a variant of trichofolliculoma, is a rare disease that clinically show a centrally depressed lesion usually singly on the nose, and histologically a centrally located cavity, lined by squamous epithelium, with numerous sebaceous lobules connected to them. We describe a case of sebaceous trichofolliculoma in a 27-year-old woman who had several brown papules on the nose. We think that this is the first report of sebaceous trichofolliculloma in Korean literature.


Assuntos
Adulto , Feminino , Humanos , Epitélio , Nariz , Doenças Raras
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