Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Añadir filtros








Intervalo de año
1.
Korean Journal of Dermatology ; : 124-127, 2005.
Artículo en Coreano | WPRIM | ID: wpr-64492

RESUMEN

We report a case of subcutaneous phaeohyphomycosis caused by Exophiala (E.) jeanselmei in a 75-year-old female, who showed subcutaneous abscesses on the both forearms for 8 months. Histopathologically, suppurative granulomatous inflammation and short hyphae & spores were observed. Fungal culture grew out the typical black-gray velvety colonies of E. jeanselmei after 3 weeks. The isolate grew well at 25degrees C, but very poorly at 37degrees C. No growth could be observed at 40degrees C. We confirmed E. jeanselmei by colony & microscopic morphology and temperature tolerance test. The patient had been treated with fluconazole for 3 months.


Asunto(s)
Anciano , Femenino , Humanos , Absceso , Exophiala , Fluconazol , Antebrazo , Hifa , Inflamación , Feohifomicosis , Esporas
2.
Korean Journal of Dermatology ; : 1225-1227, 2004.
Artículo en Coreano | WPRIM | ID: wpr-60824

RESUMEN

Pyogenic granuloma is a benign vascular tumor related to trauma, infection, or hormonal changes. When it affects the oral cavity, the most frequent site is the gingiva and involvement of the tongue is very rare. Occurrence of pyogenic granuloma on the fissured tongue has not been reported yet. We present a rare case of pyogenic granuloma on the tongue in a 64 year old female patient in which the fissured tongue seemed to play important roles in the pathogenesis of occurrence of the pyogenic granuloma.


Asunto(s)
Femenino , Humanos , Persona de Mediana Edad , Encía , Granuloma Piogénico , Boca , Lengua , Lengua Fisurada
3.
Annals of Dermatology ; : 292-294, 2000.
Artículo en Inglés | WPRIM | ID: wpr-73459

RESUMEN

A 53-year-old man had skin-colored linear serpiginous plaque within brownish patch on his left thigh for one year. He habitually drank natural spring water for 3 years. We diagnosed this case as sparganosis infiltrated within dermis by histologic and parasitologic diagnosis. The skin lesion mimicked the cutaneous larva migrans by showing dermal migration of sparganum to pro-duce itchy linear serpiginous plaque. We report an interesting case of sparganosis mimicking cutaneous larva migrans.


Asunto(s)
Humanos , Persona de Mediana Edad , Dermis , Diagnóstico , Larva Migrans , Manantiales Naturales , Piel , Esparganosis , Plerocercoide , Muslo , Agua
4.
Annals of Dermatology ; : 53-55, 1998.
Artículo en Inglés | WPRIM | ID: wpr-66296

RESUMEN

Molluscum contagiosum is a common, benign, viral disease of the skin and mucous membrane that generally affects children. This disease is characterized by a 2 to 7 week incubation period; the involvement of the face, trunk, and extremities; spontaneous resolution within 2 to 4 months; and common autoinoculation. Individuals are susceptibile from the age of one. Herein, we report a case of molluscum contagiosum with an unusual manifestation. The skin lesions, which occured at ten days postpartum, showed two adjacent hard papules on the posterior scalp. They remained for 8 months in the same size and number.


Asunto(s)
Niño , Humanos , Recién Nacido , Extremidades , Molusco Contagioso , Membrana Mucosa , Periodo Posparto , Cuero Cabelludo , Piel , Virosis
5.
Annals of Dermatology ; : 285-288, 1998.
Artículo en Inglés | WPRIM | ID: wpr-51031

RESUMEN

Partial Unilateral Lentiginosis (PUL) is a rare pigmentary disorder characterized by the numerous lentigines confined to a body segment, with a sharp demarcation at the midline. We report two cases of PUL. A 38-year-old woman had asymptomatic discrete small hyperpigmented macules that were scattered on the T7~L1 dermatomes on the left side of her trunk and were clearly demarcated in the midline on both anterior and posterior sides. In the other case, an 18- year-old woman had hyperpigmented macules that were scattered on the left neck, shoulder, and anterior chest. Other anomalies including neurofibromatosis, neurologic anomalies, and multiple lentiginous syndrome were not related in both cases. We report two cases of PUL having no other anomalies.


Asunto(s)
Adulto , Femenino , Humanos , Lentigo , Cuello , Neurofibromatosis , Hombro , Tórax
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA