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
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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