Pseudomyxoma peritonei (PMP) – a rare entity

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dc.contributor.author Ebrahim, Zaeem I.
dc.contributor.author Lockhat, Zarina I.
dc.contributor.author Ismail, Farzanah
dc.date.accessioned 2011-09-02T07:51:17Z
dc.date.available 2011-09-02T07:51:17Z
dc.date.issued 2011-09
dc.description.abstract Pseudomyxoma peritonei (PMP) is a rare complication of mucinous tumours of appendiceal or ovarian origin that results in peritoneal and omental implants. Clinical morbidity and mortality arise from the fact that copious amounts of extracellular and peritoneal mucin result in distortion and loss of function of visceral organs. Therapeutic paracentesis is not possible because of the nature of the mucin. Currently, new techniques are being used to attempt to debulk the mucin volume; none, however, has lead to superior outcome. en_US
dc.description.uri http://www.sajr.org.za/index.php/sajr en_US
dc.identifier.citation Ebrahim, ZI, Lockhat, ZI & Ismail, F 2011, 'Pseudomyxoma peritonei (PMP) - a rare entity', South African Journal of Radiology, vol. 15, no. 3, pp. 79-81. en_US
dc.identifier.issn 1027-202X
dc.identifier.uri http://hdl.handle.net/2263/17211
dc.language.iso en en_US
dc.publisher Health and Medical Publishing Group en_US
dc.rights Health and Medical Publishing Group en_US
dc.subject Pseudomyxoma peritonei (PMP) en_US
dc.subject.lcsh Ovaries -- Tumors en
dc.subject.lcsh Appendix (Anatomy) -- Tumors en
dc.subject.lcsh Mucins -- Diseases en
dc.title Pseudomyxoma peritonei (PMP) – a rare entity en_US
dc.type Article en_US


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