Results 201 to 210 of about 20,954 (250)
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JAMA Surgery, 2023
Importance Pseudomyxoma peritoni, a rare condition characterized by mucinous ascites and peritoneal deposits, mainly originates from a ruptured mucinous appendix tumor and is considered an indolent disease but can progress and become fatal.
K. Chandrakumaran +4 more
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Importance Pseudomyxoma peritoni, a rare condition characterized by mucinous ascites and peritoneal deposits, mainly originates from a ruptured mucinous appendix tumor and is considered an indolent disease but can progress and become fatal.
K. Chandrakumaran +4 more
semanticscholar +1 more source
BMJ Case Reports, 2023
Cystic mesothelioma, also known as benign multicystic peritoneal mesothelioma (BMPM), is a rare neoplasm and one of the five main histological types of peritoneal mesothelioma.
Ceylan Altıntaş Taşlıçay +3 more
semanticscholar +1 more source
Cystic mesothelioma, also known as benign multicystic peritoneal mesothelioma (BMPM), is a rare neoplasm and one of the five main histological types of peritoneal mesothelioma.
Ceylan Altıntaş Taşlıçay +3 more
semanticscholar +1 more source
Low-grade mucinous neoplasm arising from mature ovarian teratoma with pseudomyxoma peritonei
International Journal of Gynecological Cancer, 2023Mucinous neoplasms involving the ovary are challenging, as metastases frequently simulate primary ovarian tumors clinically and histologically. When associated with pseudomyxoma peritonei, a gastrointestinal primary is more likely, most commonly ...
Ridin Balakrishnan +2 more
semanticscholar +1 more source
Archives of Surgery, 1980
Thirty-eight patients with pseudomyxoma peritonei were treated at the M. D. Anderson Hospital, Houston, from 1954 to 1978. The various treatment regimens used have provided actuarial survival rates of 54% at five years and 18% at ten years. Local or regional disease was the cause of death in 68% of patients, and no patient died of metastatic disease ...
R N, Fernandez, J M, Daly
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Thirty-eight patients with pseudomyxoma peritonei were treated at the M. D. Anderson Hospital, Houston, from 1954 to 1978. The various treatment regimens used have provided actuarial survival rates of 54% at five years and 18% at ten years. Local or regional disease was the cause of death in 68% of patients, and no patient died of metastatic disease ...
R N, Fernandez, J M, Daly
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European Journal of Surgical Oncology, 2020
Pseudomyxoma Peritonei (PMP) is a rare peritoneal malignancy, most commonly originating from a perforated epithelial tumour of the appendix. Given its rarity, randomized controlled trials on treatment strategies are lacking, nor likely to be performed in
K. Govaerts +36 more
semanticscholar +1 more source
Pseudomyxoma Peritonei (PMP) is a rare peritoneal malignancy, most commonly originating from a perforated epithelial tumour of the appendix. Given its rarity, randomized controlled trials on treatment strategies are lacking, nor likely to be performed in
K. Govaerts +36 more
semanticscholar +1 more source
Prognostic Impact of Pathology, Cytoreduction, and Tumor Markers in Pseudomyxoma Peritonei.
Journal of Surgical Research, 2022INTRODUCTION The pathologic classification of pseudomyxoma peritonei is controversial. This study aimed to standardize the histopathological evaluation of pseudomyxoma peritonei and identify the clinicopathological factors associated with survival ...
A. Lopes +4 more
semanticscholar +1 more source
Cancer Treatment Reviews, 2007
Pseudomyxoma peritonei (PMP) is a rare condition, which is known for its high mortality when not treated properly. The first step to improve prognosis of these patients is to recognize this clinical syndrome preferably in an early stage. Knowledge of pathogenesis and common diagnostic tools is essential in this regard. Treatment strategy for PMP should
R M, Smeenk +2 more
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Pseudomyxoma peritonei (PMP) is a rare condition, which is known for its high mortality when not treated properly. The first step to improve prognosis of these patients is to recognize this clinical syndrome preferably in an early stage. Knowledge of pathogenesis and common diagnostic tools is essential in this regard. Treatment strategy for PMP should
R M, Smeenk +2 more
openaire +3 more sources
Clinical Oncology, 2003
Pseudomyxoma peritonei is a rare form of mucinous ascites associated with peritoneal and omental implants. The origin is controversial, and recent immunohistochemical and molecular genetic evidence suggests the appendix to be the likely site. The condition often presents as an incidental finding at laparotomy.
R, Harshen, R, Jyothirmayi, N, Mithal
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Pseudomyxoma peritonei is a rare form of mucinous ascites associated with peritoneal and omental implants. The origin is controversial, and recent immunohistochemical and molecular genetic evidence suggests the appendix to be the likely site. The condition often presents as an incidental finding at laparotomy.
R, Harshen, R, Jyothirmayi, N, Mithal
openaire +2 more sources
American Journal of Surgery, 2021
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.
S. Reiter +3 more
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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.
S. Reiter +3 more
semanticscholar +1 more source
Diseases of the Colon & Rectum, 1972
Pseudomyxoma peritonei is a rare condition that develops following rupture of a mucocele of the appendix or the ovary. Twelve cases have been reviewed. Early diagnosis and aggressive surgery offer the best chance for survival of the patient. Recurrent intestinal obstruction is a part of the natural course of the disease, and should be treated ...
B C, Ghosh, A G, Huvos, H W, Whiteley
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Pseudomyxoma peritonei is a rare condition that develops following rupture of a mucocele of the appendix or the ovary. Twelve cases have been reviewed. Early diagnosis and aggressive surgery offer the best chance for survival of the patient. Recurrent intestinal obstruction is a part of the natural course of the disease, and should be treated ...
B C, Ghosh, A G, Huvos, H W, Whiteley
openaire +2 more sources

