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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 Jyothirmayi
exaly +3 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 Jyothirmayi
exaly +3 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 ...
P, Pfitzer, G, Richartz
exaly +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
F A N Zoetmulder, V J Verwaal
exaly +3 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
F A N Zoetmulder, V J Verwaal
exaly +3 more sources
BJOG: An International Journal of Obstetrics & Gynaecology, 1996
Pseudomyxoma peritonei is a clinical entity that has lead to much confusion about its etiology, clinical manifestations, treatment, and prognosis. Pseudomyxoma peritonei is currently defined as a grade I mucinous adenocarcinoma that arises from a primary appendiceal adenoma. The clinical entity is defined by a redistribution phenomenon. This means that
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Pseudomyxoma peritonei is a clinical entity that has lead to much confusion about its etiology, clinical manifestations, treatment, and prognosis. Pseudomyxoma peritonei is currently defined as a grade I mucinous adenocarcinoma that arises from a primary appendiceal adenoma. The clinical entity is defined by a redistribution phenomenon. This means that
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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
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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
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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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Coloproctology, 1997
Pseudomyxoma peritonei is characterized by mucinous ascites and implants throughout the abdominal cavity. Although not a typical malignant entity the disease shows a long-term poor prognosis, because mucinous implants cannot be resected radically. Additional therapy is not able to improve the prognosis.
R. Frese +3 more
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Pseudomyxoma peritonei is characterized by mucinous ascites and implants throughout the abdominal cavity. Although not a typical malignant entity the disease shows a long-term poor prognosis, because mucinous implants cannot be resected radically. Additional therapy is not able to improve the prognosis.
R. Frese +3 more
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Ugeskrift for laeger, 2004
Udgivelsesdato: 2004-Aug ...
Iversen, Lene Hjerrild; id_orcid 0000-0002-2336-2923 +4 more
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Udgivelsesdato: 2004-Aug ...
Iversen, Lene Hjerrild; id_orcid 0000-0002-2336-2923 +4 more
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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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Unusual origins of pseudomyxoma peritonei
Journal of Surgical Oncology, 2000Pseudomyxoma peritonei is a rare neoplastic condition in that gelatinous intraperitoneal fluid collections and mucinous implants on the peritoneal surfaces and omentum are found. The pathological origin is usually an adenoma or well-differentiated adenocarcinoma of the appendix. A smaller number of cases arises from ovarian tumors.
de Bree, E. +3 more
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