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Published in 2019 at "Diagnostic Cytopathology"
DOI: 10.1002/dc.24262
Abstract: Pseudomyxoma peritonei (PMP) is a rare condition characterized by intraperitoneal accumulation of mucus due to mucinous neoplasia. The characteristic cytological feature of PMP in the ascites is abundant mucus with or without epithelial cell clusters.… read more here.
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Published in 2021 at "International Journal of Cancer"
DOI: 10.1002/ijc.33460
Abstract: Pseudomyxoma peritonei (PMP) is a rare disorder with unique pathological and genetic changes. Although several studies have reported the clinical features and mutational changes of PMP that originates from the appendix, few studies on PMP… read more here.
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Published in 2019 at "European Radiology"
DOI: 10.1007/s00330-019-06102-1
Abstract: ObjectivesThe peritoneal cancer index (PCI) is widely used for assessing pseudomyxoma peritonei (PMP) in surgery. The aim of this study was to evaluate the utility of a modified PCI using 18F-fluorodeoxyglucose (18F-FDG)-PET/CT (PET-PCI) for predicting… read more here.
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Published in 2020 at "Journal of Cancer Research and Clinical Oncology"
DOI: 10.1007/s00432-020-03321-8
Abstract: Pseudomyxoma peritonei (PMP) is a rare clinical malignancy syndrome characterized by the uncontrollable accumulation of copious mucinous ascites in the peritoneal cavity, resulting in “jelly belly”. The mechanism of tumor progression and mucin hypersecretion remains… read more here.
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Published in 2019 at "International Journal of Clinical Oncology"
DOI: 10.1007/s10147-019-01592-x
Abstract: Background Pseudomyxoma peritonei (PMP) is a rare malignancy, and there is insufficient evidence about systemic chemotherapy for this disease. Methods We retrospectively evaluated the efficacy and safety of a chemotherapeutic regimen with 5-fluorouracil and oxaliplatin… read more here.
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Published in 2019 at "Journal of Gastrointestinal Cancer"
DOI: 10.1007/s12029-018-00192-8
Abstract: Pseudomyxoma peritonei (PMP) is a disorder characterized by an intra-abdominal accumulation of mucin secondary to the growth of neoplastic mucin-secreting cells on peritoneal surfaces [1, 2]. PMP is a rare condition with an estimated incidence… read more here.
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Published in 2019 at "Indian Journal of Surgery"
DOI: 10.1007/s12262-019-01978-1
Abstract: Primary mucinous cystadenocarcinoma of the spleen is an extremely rare tumour. Only 7 cases have been reported in the literature. Mucinous cystadenocarcinoma of the spleen presenting as pseudomyxoma peritonei has been reported only once. Our… read more here.
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Published in 2021 at "American journal of surgery"
DOI: 10.1016/j.amjsurg.2021.12.003
Abstract: BACKGROUND The discovery of a low grade appendiceal mucinous neoplasm (LAMN) during appendectomy is a rare scenario. These neoplasms can progress to pseudomyxoma peritonei (PMP), however the incidence of progression is not well known. METHODS… read more here.
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Published in 2019 at "Clinical colorectal cancer"
DOI: 10.1016/j.clcc.2019.03.002
Abstract: BACKGROUND No standard treatment for advanced unresectable pseudomyxoma peritonei (PMP) has been defined so far. PMP is traditionally considered chemoresistant but nonrandomized series showed promising results with regimens for gastrointestinal tumors. PATIENTS AND METHODS We… read more here.
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Published in 2020 at "International Journal of Surgery Case Reports"
DOI: 10.1016/j.ijscr.2020.05.072
Abstract: Highlights • Completeness of cytoreduction is the key factor for long term survival in pseudomyxoma peritonei.• Neoadjuvant chemotherapy for unresectable cases of PMP has been tried but often with discouraging results.• Intraperitoneal administration of chemotherapy… read more here.
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Published in 2017 at "Medicine"
DOI: 10.1097/md.0000000000007548
Abstract: Rationale: Pseudomyxoma peritonei is an unusual clinical condition, and the appendix and ovaries are reported as the primary sites. Patient concerns: A 44-year-old man who was reported a 3-month history of lower abdominal pain and… read more here.