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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
exaly +5 more sources
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
exaly +5 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
openaire +4 more sources
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 +4 more sources
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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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
openaire +2 more sources
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
Der Onkologe, 2015
Hintergrund Mit einer Inzidenz von 1 bis 2 Erkrankungen pro 1.000.000 Einwohner pro Jahr stellt das Pseudomyxoma peritonei (PMP) eine extrem seltene Erkrankung dar. Haufigster Ursprungsort des PMP ist die muzinose Neoplasie der Appendix. Andere intra- und extraabdominale Organe kommen als Primarius weitaus seltener vor.
L. März, P. Piso
openaire +1 more source
Hintergrund Mit einer Inzidenz von 1 bis 2 Erkrankungen pro 1.000.000 Einwohner pro Jahr stellt das Pseudomyxoma peritonei (PMP) eine extrem seltene Erkrankung dar. Haufigster Ursprungsort des PMP ist die muzinose Neoplasie der Appendix. Andere intra- und extraabdominale Organe kommen als Primarius weitaus seltener vor.
L. März, P. Piso
openaire +1 more source
Pseudomyxoma peritonei peritonitis
BMJ Case ReportsPseudomyxoma peritonei (PMP) is a rare neoplastic condition characterised by gelatinous ascites, which generally arise from mucin-producing appendiceal tumours. Presentation is variable but requires prompt recognition to ensure appropriate specialist management due to risk of malignancy.
Pranathi Yannamani +3 more
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