Doege-Potter syndrome associated to metastatic solitary fibrous tumor

Autor: Andrade, Matheus de Oliveira, Sousa, Nathália da Cruz de, Amaral, Paulo Siqueira do, Costa, Samantha Cabral Severino da, Lima, Luiz Guilherme Cernaglia Aureliano de, Lourenço Júnior, Delmar Muniz, Feher, Olavo

Publikováno v: Autopsy and Case Reports, Volume: 12, Article number: e2021412, Published: 16 DEC 2022

Solitary fibrous tumor (SFT) is a rare fibroblastic mesenchymal neoplasm with an estimated annual incidence of 0.35 per 100,000 individuals. Doege-Potter syndrome is a paraneoplastic syndrome related to solitary fibrous tumor clinically characterized

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______608::88ca08424ee8a764f05798ca8932bca3
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602022000100720&lng=en&tlng=en

Healing of tumor-induced osteomalacia as assessed by high-resolution peripheral quantitative computed tomography is not similar across the skeleton in the first years following complete tumor excision

Autor: Salles Rosa Neto, Nilton, Pereira, Rosa Maria Rodrigues, Yuki, Emily Figueiredo Neves, Souza, Fernando Henrique Carlos de, Takayama, Liliam, Carneiro, Maria Inez da Silveira, Lima, Luiz Guilherme Cernaglia Aureliano de, Ishy, Augusto, Elias, Alexandre José Reis

Publikováno v: In Bone Reports June 2024 21

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tumor Reduction with Pazopanib in a Patient with Recurrent Lumbar Chordoma

Autor: Ribeiro, Maurício Fernando Silva Almeida, de Sousa, Micelange Carvalho, Hanna, Samir Abdallah, Maldaun, Marcos Vinicius Calfat, Kurimori, Ceci Obara, de Lima, Luiz Guilherme Cernaglia Aureliano, Mattedi, Romulo Loss, Munhoz, Rodrigo Ramella

Publikováno v: Case Reports in Oncological Medicine.

Introduction. Chordomas are rare malignancies of bone origin that occur in the axial skeleton, typically the skull base and lumbar/sacral regions. Although often classified as low-grade neoplasms, its locally infiltrative behavior may result in signi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=hindawi_publ::9c6d65c407d4f9cc8770b28475b55479

Tumor neuroendócrino do canal anal

Autor: Christiano,Adriana Borgonovi, Gullo,Caio Eduardo, Palmejani,Marianna Angelo, Marques,Aline Maria de Vita, Barbosa,Amanda Pires, Basso,Marcelo Pandolfi, Lima,Luiz Guilherme Cernaglia Aureliano de, Netinho,João Gomes

Publikováno v: Jornal Português de Gastrenterologia, Volume: 19, Issue: 5, Pages: 267-269, Published: SEP 2012
Jornal Português de Gastrenterologia v.19 n.5 2012
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

We report a rare case of neuroendocrine tumor of the anal canal and its poor prognosis, plus discuss the need of immunohistochemical for an acurate diagnosis and to guide treatment. Relatamos um caso raro de tumor neuroendócrino do canal anal e seu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bd3132822ae94c0495537c778d32e81a
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-81782012000500011&lng=en&tlng=en