1999
DOI: 10.1023/a:1026622111220
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Cited by 15 publications
(3 citation statements)
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“…Primary cystadenocarcinoma of the spleen is extremely rare. All the reported cases were mucinous type [2], [4], [5], [6], [7], [8], [9]. The hypothesized origins of these tumors include (1) ectopic pancreatic tissue; (2) ectopic intestinal tissue; and (3) invaginated mesothelium of the splenic capsule [2], [6].…”
Section: Discussionmentioning
confidence: 99%
“…Primary cystadenocarcinoma of the spleen is extremely rare. All the reported cases were mucinous type [2], [4], [5], [6], [7], [8], [9]. The hypothesized origins of these tumors include (1) ectopic pancreatic tissue; (2) ectopic intestinal tissue; and (3) invaginated mesothelium of the splenic capsule [2], [6].…”
Section: Discussionmentioning
confidence: 99%
“…Primary mucinous cystadenoma of spleen is an extremely rare finding [3,4,6,7]. The exact histogenetic mechanism of splenic mucinous cystic tumors is unknown except those arising from heterotopic pancreatic tissues [1].…”
Section: Discussionmentioning
confidence: 99%
“…The exact histogenetic mechanism of splenic mucinous cystic tumors is unknown except those arising from heterotopic pancreatic tissues [1]. However, mucinous cysts are usually found in association with the cystadenoma of pancreas, pseudomyxoma peritonei and mucocele of appendix [7]. Only few cases, in which the tissue of origin was un-defined, are documented in the literature [3-7].…”
Section: Discussionmentioning
confidence: 99%