Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Márcia Lanzoni de Alvarenga Lira"'
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 99, Iss 5, Pp 740-742 (2024)
Externí odkaz:
https://doaj.org/article/b99610fab29446058c0e6b1b472d31bf
Autor:
Carolina Forte Amarante, Livia Mendes Sabia Acedo, Fátima Maria de Oliveira Rabay, Benedito do Espírito Santo Campos, Márcia Lanzoni de Alvarenga Lira, Samuel Henrique Mandelbaum
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 90, Iss 3 suppl 1, Pp 121-124 (2015)
AbstractTNF alpha antagonist-induced lupus-like syndrome is a rare condition which predominantly affects women (4:1). The average age of onset is 46-51 years. It occurs after exposure to TNF alpha antagonist and disappears after discontinuation of su
Externí odkaz:
https://doaj.org/article/37169c4d4612449b9ed8181c1caa45e9
Autor:
Denise Camargo Cirvidiu, Beatriz Lopes Ferraz Elias, Juliana Chaib Ferraira Jorge, Márcia Lanzoni de Alvarenga Lira, Samuel Henrique Mandelbaum
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 90, Iss 4, Pp 561-563 (2015)
AbstractErythema elevatum diutinum is a rare chronic leukocytoclastic vasculitis of unknown etiology. It is believed to be due to deposition of immune complexes in the vessels. Clinically it is manifested as erythematous violaceous papules and nodule
Externí odkaz:
https://doaj.org/article/4202a928d44d4422811e62f31b557b7a
Autor:
Felipe Siqueira Ramos, Flávia Regina Ferreira, Fátima Maria de Oliveira Rabay, Marcia Lanzoni de Alvarenga Lira
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 93, Iss 5, Pp 730-732 (2018)
Abstract: Neutrophilic dermatosis of the dorsal hands is considered a rare and localized variant of Sweet's syndrome. Although the etiology is unknown, there are reports of association with infections, neoplasias, autoimmune diseases and medications.
Externí odkaz:
https://doaj.org/article/2c89f0189b6a4e5cbea389835a644895
Autor:
Flávia Regina Ferreira, Leopoldo Duailibe Nogueira Santos, Fernando Augusto Nogueira Mendes Tagliarini, Marcia Lanzoni de Alvarenga Lira
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 88, Iss 6 suppl 1, Pp 179-182 (2013)
Porokeratosis is a disorder of epidermal keratinization characterized by annular plaques with an atrophic center and hyperkeratotic edges, and includes a heterogeneous group of disorders that are mostly inherited in an autosomal dominant form. This r
Externí odkaz:
https://doaj.org/article/af83a3131a974c6984d17265b5a5f813
Autor:
Priscila Pacheco Lessa, Juliana Chaib Ferreira Jorge, Flávia Regina Ferreira, Marcia Lanzoni de Alvarenga Lira, Samuel Henrique Mandelbaum
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 88, Iss 6 suppl 1, Pp 39-43 (2013)
The authors describe a case of a female patient with Acral Pseudolymphomatous Angiokeratoma of Children, known as APACHE. It is a rare benign cutaneous disease, of unknown etiology, characterized by multiple, asymptomatic erythematous-violaceous papu
Externí odkaz:
https://doaj.org/article/2d13c6b78db44ea19e43f80a7c16a797
Autor:
Flavia Regina Ferreira, Bruna da Costa Pevide, Rafaela Fabri Rodrigues, Luiz Fernando Costa Nascimento, Marcia Lanzoni de Alvarenga Lira
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 88, Iss 5, Pp 726-730 (2013)
BACKGROUND: Basal cell carcinoma is the most common form of cancer in humans. OBJECTIVES: To identify the epidemiology of basal cell carcinoma in Taubaté-SP and verify a possible association between topography and the different histological subtypes
Externí odkaz:
https://doaj.org/article/07a2cba69c8b4002b2ec2f5313fad9dc