Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Maurizio Brotto"'
Autor:
Harri Foster-Davies, BA Cantab, MB BChir, Zita M. Jessop, MA Cantab, MB BChir, MRCS, PhD, Rachel M. Clancy, MBChB, MA, MEd, FRCS, Kerrin Vijayasurej, MBChB, BSc, Johanne Vass, BSc, MSc, Thomas Bragg, MBChB, FRCS, Maurizio Brotto, MD, FRCPath, MSc
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 9, Iss 3, p e3482 (2021)
Summary:. Ossifying fibromyxoid tumor of soft parts (OFMT) is a rare mesenchymal neoplasm of uncertain lineage. OMFT normally has a benign clinical course, and malignant variants are considered unusual. Criteria defining malignancy have not yet been
Externí odkaz:
https://doaj.org/article/5b0004d0046a473dbddb633f510bf52c
Autor:
Maurizio Brotto, Paola Rucci, Alberto Righi, Sofia Asioli, Claudio Agostinelli, Giuseppe Viale, S Asioli, Maria Pia Foschini, Luca Morandi, Angelo Gianluca Corradini, Anna Sapino, Marica Iommi
Publikováno v:
Histopathology. 77:293-302
Aims A wide range of post-radiotherapy (RT) vascular lesions can occur, ranging from benign lymphangiomatous papules of the skin (BLAPs), to atypical vascular lesions (AVLs) and post-RT angiosarcomas (ASs). The relationship between benign and maligna
Autor:
Zita M. Jessop, Kerrin Vijayasurej, Maurizio Brotto, Harri Foster-Davies, Johanne Vass, Thomas Bragg, Rachel Clancy
Publikováno v:
Plastic and Reconstructive Surgery Global Open
Plastic and Reconstructive Surgery, Global Open, Vol 9, Iss 3, p e3482 (2021)
Plastic and Reconstructive Surgery, Global Open, Vol 9, Iss 3, p e3482 (2021)
Summary:. Ossifying fibromyxoid tumor of soft parts (OFMT) is a rare mesenchymal neoplasm of uncertain lineage. OMFT normally has a benign clinical course, and malignant variants are considered unusual. Criteria defining malignancy have not yet been
Autor:
Helen Daniels, Rachel Thomas, Torsten Hildebrandt, Rhiannon Clegg, Bryony Coupe, Claire Morgan, Jason Griffiths, Maurizio Brotto, Ruth Young
Genomic medicine is transforming the way in which we understand health and disease, particularly rare diseases and cancer. Rapid advances in DNA sequencing are having major implications for patients in terms of diagnosis, treatment and prognosis, pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89642a5f6a8d124dcc11ea2d27ed2a66
https://cronfa.swan.ac.uk/Record/cronfa52382
https://cronfa.swan.ac.uk/Record/cronfa52382
Publikováno v:
International Journal of Surgery Case Reports
Highlights • Phyllodes tumour is a rare type of breast tumour, accounting for less than 1% of benign and malignant breast tumours. • Phyllodes tumour is classified pathologically as benign, borderline or malignant. • Phyllodes tumour with ducta
Autor:
Camillo Orsini, Emilio Morpurgo, Sara Maria Tosato, Barbara Termini, Valerio Masiero, Annibale DʼAnnibale, Maurizio Brotto
Publikováno v:
Journal of Pelvic Medicine and Surgery. 14:51-55
Publikováno v:
BMJ Case Reports. :bcr-2017
A 70-year-old man was referred to plastic surgery with a progressively enlarging lesion to his forehead. A small nodule had been present since 30 years. The patient had presented to his general practitioner at the time and had been reassured that thi
Autor:
Camillo Orsini, Maurizio Brotto
Publikováno v:
Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]. 33(10)
BACKGROUND During the past 10 years, sclerotherapy has radically changed, the foam sclerotherapy method being better than that of liquid sclerotherapy. OBJECTIVES We have analyzed the immediate pathologic effects on the saphenous vein wall in vivo af
Publikováno v:
Ultrastructural pathology. 28(3)
A granular cell tumor (GCT) in a 39-year-old white man is reported. It was localized in the intrapancreatic part of the common bile duct and caused obstruction of the bile downflow. The patient underwent radical surgical procedures because a malignan