Multiple cavitary pulmonary nodules in association with pyoderma gangrenosum: case report Múltiplos nódulos pulmonares cavitados em associação com pioderma gangrenoso: relato de caso

Autor: Maraya de Jesus Semblano Bittencourt, Luciana Fontenele Brito Soares, Lilia Sampaio Lobato, Alexandre Dias Mançano, Helandro Stuart Castro Leandro, Diana Mendes da Fonseca

Publikováno v: Anais Brasileiros de Dermatologia, Vol 87, Iss 2, Pp 301-304 (2012)

Pyoderma gangrenosum is a rare neutrophilic disease of unknown origin that is associated with systemic diseases in 50% of cases. It is characterized by erythematous-violaceous nodular lesions that quickly progress to painful ulcers, with undermined e

Externí odkaz: https://doaj.org/article/f150d8fb318d4311b49e4e56963cf2e4

Granuloma anular elastolítico gigantocelular: relato de caso Annular elastolytic giant cell granuloma: case report

Autor: Rossana Ruth da Veiga Gonçalves, Mario Fernando Ribeiro de Miranda, Fernanda de Oliveira Viana, Luíza Helena dos Santos Cavaleiro, Diana Mendes da Fonseca

Publikováno v: Anais Brasileiros de Dermatologia, Vol 86, Iss 4, Pp 69-71 (2011)

O granuloma anular elastolítico gigantocelular é dermatose granulomatosa rara, caracterizada, histologicamente, por fagocitose das fibras elásticas por células gigantes multinucleadas e, clinicamente, por placas anulares com bordas elevadas e cen

Externí odkaz: https://doaj.org/article/fd3697ea9441481793e39f5b257f9875

Multiple cavitary pulmonary nodules in association with pyoderma gangrenosum: case report

Autor: Helandro Stuart Castro Leandro, Alexandre Dias Mançano, Lilia Sampaio Lobato, Diana Mendes da Fonseca, Luciana Fontenele Brito Soares, Maraya de Jesus Semblano Bittencourt

Publikováno v: Anais Brasileiros de Dermatologia, Volume: 87, Issue: 2, Pages: 301-304, Published: APR 2012
Anais Brasileiros de Dermatologia v.87 n.2 2012
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD

Pyoderma gangrenosum is a rare neutrophilic disease of unknown origin that is associated with systemic diseases in 50% of cases. It is characterized by erythematous-violaceous nodular lesions that quickly progress to painful ulcers, with undermined e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a749f8d4675afad43b193909bd55b7f
https://doi.org/10.1590/s0365-05962012000200018

Do you know this syndrome? Xeroderma pigmentosum (XP)

Autor: Fernanda de Oliveira, Viana, Luíza Helena dos Santos, Cavaleiro, Clívia Maria Moraes de Oliveira, Carneiro, Maraya de Jesus Semblano, Bittencourt, Renata Silva, Barros, Diana Mendes da, Fonseca

Publikováno v: Anais brasileiros de dermatologia. 86(5)

Xeroderma pigmentosum is a rare genetic disease characterized by clinical and cellular hypersensitivity to ultraviolet radiation and DNA repair defects. Patients with xeroderma pigmentosum experience sun-induced cutaneous and ocular abnormalities, in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c171d947fe018361a9ca7e02f0f8d291
https://pubmed.ncbi.nlm.nih.gov/22147055

Annular elastolytic giant cell granuloma--case report

Autor: Rossana Ruth da Veiga, Gonçalves, Mario Fernando Ribeiro de, Miranda, Fernanda de Oliveira, Viana, Luíza Helena dos Santos, Cavaleiro, Diana Mendes da, Fonseca

Publikováno v: Anais brasileiros de dermatologia. 86(4 Suppl 1)

Annular elastolytic giant cell granuloma is a rare granulomatous skin disease characterized histologically by phagocytosis of elastic fibers by multinucleated giant cells and clinically by annular patches with elevated borders and atrophic centers fo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d64d569133cdf70a38daf7f5d42f5fd2
https://pubmed.ncbi.nlm.nih.gov/22068775