Peritoneal mesothelioma: PSOGI/EURACAN clinical practice guidelines for diagnosis, treatment and follow-up
Diagnostic Imaging
Mesothelioma
03 medical and health sciences
0302 clinical medicine
Delphi Technique
Humans
Cytoreduction Surgical Procedures
Hyperthermic Intraperitoneal Chemotherapy
Peritoneal Neoplasms
3. Good health
DOI:
10.1016/j.ejso.2020.02.011
Publication Date:
2020-03-12T18:08:30Z
AUTHORS (37)
ABSTRACT
Peritoneal mesothelioma (PM) is a rare and aggressive primary peritoneal malignancy characterized by widespread multiple metastatic tumour nodules originating from the peritoneum. The conventional classification distinguishes diffuse malignant peritoneal mesothelioma (DMPM) and border-line forms: multicystic peritoneal mesothelioma (MCPM) and well-differentiated papillary peritoneal mesothelioma (WDPPM). Despite the novel achievements in the management of PM, there is difficulty in conducting randomized trials due to its rarity and aggressive biology in many cases. As there is, a necessity to standardize diagnosis and management of PM, the Peritoneal Surface Oncology Group International (PSOGI) commissioned a steering committee to elaborate clinical guidelines.
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