Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cristina Amaglio"'
Autor:
Cristina Amaglio, Annamaria De Giorgi, Fausto Sessa, Graziella Pinotti, Francesca Rita Ogliari, Anna Maria Chiaravalli
Publikováno v:
SN Comprehensive Clinical Medicine. 3:705-709
Fibromatosis-like metaplastic breast carcinoma is an uncommon variety of breast cancer whose diagnosis could be challenging. The reported case underlines the diagnostic difficulties if abundant inflammatory cells and no in situ carcinoma or epithelio
Autor:
Silvia Uccella, Fausto Sessa, Giovanna De Vecchi, Roberta Maragliano, Eleonora Leoni, Cristina Amaglio, Laura Libera, Ileana Carnevali, Giorgio Formenti, Valeria Pensotti, Daniela Furlan, Margherita Testa
Publikováno v:
Endocrine pathology. 33(3)
Primary ovarian neuroendocrine neoplasms (Ov-NENs) are infrequent and mainly represented by well-differentiated forms (neuroendocrine tumors — NETs — or carcinoids). Poorly differentiated neuroendocrine carcinomas (Ov-NECs) are exceedingly rare a
Autor:
Domenico Iovino, Gabriele Piffaretti, Cristina Amaglio, Silvia Uccella, Giuseppe Ietto, Matteo Tozzi, Marco Franchin, Maria Cristina Cervarolo, Giulio Carcano
Publikováno v:
The Journal of Vascular Access. 21:120-124
Introduction: Plasmablastic lymphoma is a rare and aggressive neoplasm, generally associated with immunodeficiencies and related to latent Epstein-Barr virus infection. This case is the first reported case of plasmablastic lymphoma relapse in aneurys
Autor:
Jean-Philippe Brouland, Fausto Sessa, Maria Laura Tanda, E. Bianconi, Mahmoud Messerer, Stefano La Rosa, Cristina Amaglio, Nathalie Rouiller, Silvia Ippolito, Silvia Uccella
IgG4-related hypophysitis (IgG4-RH) is a rare disease, which can occur singularly or as manifestation of a systemic IgG4-related disease (IgG4-RD). Less than one hundred cases have been reported in the literature, very few of which were histopatholog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82fa608701790480780201340014fbac
http://hdl.handle.net/11383/2078295
http://hdl.handle.net/11383/2078295
Lymphoproliferative disorders (LPDs) rarely involve the endocrine system, either as dissemination of a systemic condition, or as primary diseases. Due to their rarity, LPDs of endocrine organs can represent a diagnostic challenge for both pathologist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fe9f469c85965d1a3d0b237d4782444
http://hdl.handle.net/11383/2079910
http://hdl.handle.net/11383/2079910