Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Paula Carolina Pessanha de Faria"'
Autor:
Paula Carolina Pessanha de Faria, Camila Caberlon Cruz, Luna Azulay Abulafia, Juan Manuel Pineiro Maceira, Flávia de Freire Cassia, Paula Mota Medeiros
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 92, Iss 5 suppl 1, Pp 145-147 (2017)
Abstract Pemphigus herpetiformis is an autoimmune bullous disease, that combines clinical features of dermatitis herpetiformis and linear IgA bullous dermatosis and immunological characteristics of pemphigus, which makes this disease peculiar and thi
Externí odkaz:
https://doaj.org/article/c9422ab0ab9e436ea7d17a863146715a
Autor:
Paula Mota Medeiros, Natália Ribeiro de Magalhães Alves, Cássia Camarinha da Silva, Paula Carolina Pessanha de Faria, Carlos Baptista Barcaui, Juan Piñeiro-Maceira
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 90, Iss 3 suppl 1, Pp 39-42 (2015)
AbstractCollision tumors are characterized by the coexistence of two cancers in the same anatomical site and its pathogenesis remains controversial. Although uncommon, the association of basal cell carcinoma and melanocytic nevus is the most common a
Externí odkaz:
https://doaj.org/article/7a322a23ab67417bbd47e4cdbb388f28
Autor:
Paula Mota Medeiros, Natália Ribeiro de Magalhães Alves, Jeniffer Muñoz Trujillo, Cássia Camarinha da Silva, Paula Carolina Pessanha de Faria, Roberto Souto da Silva
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 90, Iss 3 suppl 1, Pp 62-65 (2015)
AbstractDarier's disease is a rare autosomal dominant genodermatosis. It has an estimated prevalence of 1 in 55,000 to 100,000 individuals, regardless of gender. It is characterized by multiple keratotic papules on the seborrheic areas of the trunk,
Externí odkaz:
https://doaj.org/article/b42ae389baae432bb66c8bd2e9a7779b
Autor:
Nathalie De Carvalho, Amanda Nascimento Cavalleiro de Macedo Mota, Paula Carolina Pessanha de Faria, Giovanni Pellacani, Carlos Baptista Barcaui, Daniel Fernandes Melo, Juan Piñeiro-Maceira
Publikováno v:
Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI)REFERENCES. 26(6)
Background Actinic keratosis (AK) incidence is increasing. Due to the risk of progression to squamous cell carcinoma, early detection and treatment are essential. The method stated in the European Consensus is cryotherapy, but there is no standard pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e036ffd68702d2fa2289789b670367f2
https://pubmed.ncbi.nlm.nih.gov/32592215
https://pubmed.ncbi.nlm.nih.gov/32592215
Autor:
Juan Piñeiro-Maceira, Paula Carolina Pessanha de Faria, Cássia Camarinha da Silva, Natália Ribeiro de Magalhães Alves, Paula Mota Medeiros, Carlos Baptista Barcaui
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 90, Iss 3 suppl 1, Pp 39-42 (2015)
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia
Collision tumors are characterized by the coexistence of two cancers in the same anatomical site and its pathogenesis remains controversial. Although uncommon, the association of basal cell carcinoma and melanocytic nevus is the most common among com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::919a0df1af38b937dbac14a6a8b98075
https://doi.org/10.1590/abd1806-4841.20153845
https://doi.org/10.1590/abd1806-4841.20153845
Autor:
Paula Carolina Pessanha de Faria, Maria de Fátima Guimarães Scotelaro Alves, Jeniffer Muñoz Trujillo, Natália Ribeiro de Magalhães Alves, Paula Mota Medeiros, Carla Araújo Jourdan
Publikováno v:
Surgical & Cosmetic Dermatology. 8
The granular cell tumor, also known as Abrikossoff tumor, is a rare neoplasm with controversial etiology that usually arises as a solitary benign lesion. The authors describe a case of multicentric granular cell tumor in a 13-year old patient treated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3f402d401112dbd86029b18a40be701
https://doi.org/10.5935/scd1984-8773.201681474
https://doi.org/10.5935/scd1984-8773.201681474