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1.
J Eur Acad Dermatol Venereol ; 18(6): 691-2, 2004 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15482297

RESUMO

We hereby report a case of lichen amyloidosus in a 69-year-old man unresponsive to various treatments. The patient was treated by occlusion with hydrocolloid dressings. Considerable subjective and objective improvement was observed with respect to the pruritus and cosmetic appearance. We suggest this convenient and efficacious treatment as first line therapy.


Assuntos
Amiloidose/terapia , Curativos Hidrocoloides , Erupções Liquenoides/terapia , Idoso , Humanos , Masculino
6.
J Eur Acad Dermatol Venereol ; 13(2): 137-9, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10568495

RESUMO

Occurrence of skin lesions during long-term therapy with hydroxyurea are well described, but there have been only a few case reports of longitudinal melanonychia associated with hydroxyurea treatment. We report herein longitudinal melanonychia associated with hydroxyurea therapy in a subject with essential thrombocytosis. The prolonged time lapse (1 year) between initiation of hydroxyurea therapy and the onset of the longitudinal melanonychia should be noted.


Assuntos
Hidroxiureia/efeitos adversos , Melanose/induzido quimicamente , Doenças da Unha/induzido quimicamente , Trombocitose/tratamento farmacológico , Idoso , Feminino , Humanos , Melaninas/análise , Fatores de Tempo
8.
J Am Acad Dermatol ; 41(2 Pt 2): 349-50, 1999 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10426930

RESUMO

Angiosarcoma that develops in areas of chronic lymphedema is also called Stewart-Treves syndrome. It usually appears in areas of lymphedema several years after mastectomy for breast carcinoma. Only 10% of these angiosarcomas occur in areas of chronic lymphedema as a result of another cause. We present a patient with epithelioid angiosarcoma as a rare complication of elephantiasis.


Assuntos
Elefantíase/complicações , Hemangiossarcoma/complicações , Neoplasias Cutâneas/complicações , Doença Crônica , Feminino , Hemangiossarcoma/patologia , Humanos , Pessoa de Meia-Idade , Neoplasias Cutâneas/patologia , Síndrome
13.
Australas J Dermatol ; 33(2): 97-101, 1992.
Artigo em Inglês | MEDLINE | ID: mdl-1294060

RESUMO

Hypomelanosis of Ito is an uncommon syndrome where bizarre, systematized hypopigmentation is often associated with neurological and other non-cutaneous abnormalities. We report two cases, one which was associated with laryngomalacia and sudden death (in which the parents were consanguineous), and one which was associated with episodes of loss of consciousness.


Assuntos
Transtornos da Pigmentação/patologia , Pele/patologia , Biópsia , Pré-Escolar , Feminino , Humanos , Recém-Nascido , Melaninas/deficiência , Transtornos da Pigmentação/etiologia , Transtornos da Pigmentação/metabolismo
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