Results 51 to 60 of about 9,671 (272)

Novel Perspectives in Pseudomyxoma Peritonei Treatment

open access: yesCancers, 2021
Simple Summary Pseudomyxoma Peritonei (PMP) represents a rare entity which greatly benefits from Cytoreductive Surgery (CRS) associated with Hyperthermic Intraperitoneal Chemotherapy (HIPEC).
A. Sommariva   +5 more
semanticscholar   +1 more source

Rare primary peritoneal mucinous adenocarcinoma in a 69‐year‐old man

open access: yesClinical Case Reports, 2021
Primary peritoneal mucinous adenocarcinoma is rare in men. The low‐grade tumor consisted of mucin‐producing columnar cells with minimal nuclear atypia. Relationship to pseudomyxoma peritonei and disseminated peritoneal adenomucinosis is discussed.
Fumiko Satoh, Yutaka Tsutusmi
doaj   +1 more source

Peptide vaccine targeting mutated GNAS: a potential novel treatment for pseudomyxoma peritonei

open access: yesJournal for ImmunoTherapy of Cancer, 2021
Background Pseudomyxoma peritonei (PMP) is a rare, slow-growing abdominal cancer with no efficacious treatment options in non-resectable and recurrent cases. Otherwise, rare activating mutations in the GNAS oncogene are remarkably frequent in PMP and the
K. Flatmark   +7 more
semanticscholar   +1 more source

Pseudomyxoma pleurii: unusual location of a rare disease

open access: yesRadiology Case Reports, 2021
Pseudomyxoma peritonei with pleural extension is very rare. Dissemination in the pleural cavity can be trans diaphragmatic or hematogenous. Appendicular and ovarian mucinous tumors are the most often involved.
Kaoutar Imrani   +4 more
doaj  

Pseudomyxoma peritonei – a revisit: report of 2 cases and literature review [PDF]

open access: yes, 2006
BACKGROUND: Pseudomyxoma peritonei (PMP) is a rare, chronic, relapsing, diagnostically challenging and poorly understood disease characterized by disseminated mucinous ascites and peritoneal implants.
Kanthan, Rani   +2 more
core   +3 more sources

Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Pseudomyxoma Peritonei of Appendiceal Origin: A Single Center Experience

open access: yesFrontiers in Surgery, 2021
Background: Pseudomyxoma peritonei (PMP) originating from appendiceal mucinous neoplasm is a rare peritoneal malignancy characterized by the progressive intraperitoneal accumulation of mucus leading to death if left untreated.
F. Santullo   +8 more
semanticscholar   +1 more source

Pseudomyxoma Peritonei in a Patient with History of Breast Cancer

open access: yesThe Korean Journal of Gastroenterology, 2016
Pseudomyxoma peritonei is a very rare condition, and even rarer in patients with history of cancer. A 70-year old woman with a history of breast cancer was admitted with abdominal pain and distention.
Tae Seob Jung   +6 more
doaj   +1 more source

The mutational landscape and prognostic indicators of pseudomyxoma peritonei originating from the ovary

open access: yesInternational Journal of Cancer, 2021
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 originating ...
B. Wang   +15 more
semanticscholar   +1 more source

CHALLENGES IN CHOICE OF THE TREATMENT STRATEGY FOR PATIENTS WITH RECURRENT PSEUDOMYXOMA PERITONEI

open access: yesСибирский онкологический журнал, 2019
Pseudomixoma peritonei is a rare type of peritoneal carcinomatosis accompanied by accumulation of mucus and high recurrence rate and in some cases complicated with intestinal obstruction.
A. G. Abdullaev   +2 more
doaj   +1 more source

Comprehensive Treatment Algorithms of the Swiss Peritoneal Cancer Group for Peritoneal Cancer of Gastrointestinal Origin. [PDF]

open access: yes, 2022
Peritoneal cancer (PC) is a dire finding, yet in selected patients, long-term survival is possible. Complete cytoreductive surgery (CRS) together with combination immunochemotherapy is essential to achieve cure. Hyperthermic intraperitoneal chemotherapy (
Adamina, M.   +16 more
core   +5 more sources

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