Results 161 to 170 of about 4,203 (182)
Some of the next articles are maybe not open access.
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 ...
Andrew G. Huvos +2 more
openaire +3 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 ...
Andrew G. Huvos +2 more
openaire +3 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
openaire +2 more sources
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
openaire +2 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 +2 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 +2 more sources
The Lancet, 1969
Pseudomyxoma peritonei is a term that began life as a description of a pathological entity; but now, by usage, it refers to a clinical syndrome of massive accumulation of gelatinous ascites, with long survival and an absence of lymphatic, hepatic parenchymal, and extraperitoneal spread.
D.C. Glenn, J.P. Halliday, J.M. Little
openaire +3 more sources
Pseudomyxoma peritonei is a term that began life as a description of a pathological entity; but now, by usage, it refers to a clinical syndrome of massive accumulation of gelatinous ascites, with long survival and an absence of lymphatic, hepatic parenchymal, and extraperitoneal spread.
D.C. Glenn, J.P. Halliday, J.M. Little
openaire +3 more sources
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
openaire +2 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
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 +2 more sources
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 +2 more sources
Ugeskrift for laeger, 2004
Udgivelsesdato: 2004-Aug ...
Iversen, Lene Hjerrild +4 more
openaire +2 more sources
Udgivelsesdato: 2004-Aug ...
Iversen, Lene Hjerrild +4 more
openaire +2 more sources
Cytology of pseudomyxoma peritonei
Cytopathology, 1995Cytology of pseudomyxoma peritoneiThe cytology of five cases of pseudomyxoma peritonei is described. It is characterized by large masses of mucinous material, some of which is wrapped up in a network of elongated fibroblast‐like cells. Irregular clusters of flat branching vimentin‐positive fibroblast‐like cells may be found as the disease progresses ...
G. Richartz, P. Pfitzer
openaire +3 more sources
A clinical study on pseudomyxoma peritonei
Journal of Gastroenterology and Hepatology, 1995Abstract To elucidate the clinical entity of pseudomyxoma peritonei, nine patients (male: female = 6:3) who had been treated in Chang Gung Memorial Hospital in the past 13 years were reviewed. The male patients with original appendiceal tumour were older than the male patients with original colon cancer or indefinite tumour (70, 67 and 67 years vs 42 ...
Cheng-Shyong Wu +4 more
openaire +3 more sources