Publication: Mesenteric Fibromatosis
| creativeworkseries.issn | 1812-2027 | |
| dc.contributor.author | Radhakrishna, V | |
| dc.contributor.author | Patil, RS | |
| dc.date.accessioned | 2025-10-31T07:30:43Z | |
| dc.date.available | 2025-10-31T07:30:43Z | |
| dc.date.issued | 2017 | |
| dc.description | Radhakrishna V,1 Patil RS2 1Department Paediatric Surgery Indira Gandhi Institute of Child Health, Bengaluru, India. 2Department of General Surgery Basaveshwar Hospital, MR Medical College, Gulbarga, India | |
| dc.description.abstract | ABSTRACT Mesenteric fibromatosis is a rare, locally invasive benign tumor arising from fibroblasts and fibrous tissue of mesentery. Their infiltrative nature can cause fatal visceral involvement. Most of the cases reported have an association with Gardner’s Syndrome, prolonged intake of estrogen, and previous trauma, but mesenteric fibromatosis can occur as a primary ailment without an underlying stimulant. A nineteen-year female presented with mass and pain abdomen diagnosed to have subserous fibroid but eventually turned out to be primary mesenteric fibromatosis. She underwent wide excision along with the resection of adjacent bowel. She is on follow-up with no evidence of recurrence. KEY WORDS Estradiol receptors, Fibromatosis, Mesenteric mass, Wide surgical excision | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/2967 | |
| dc.language.iso | en_US | |
| dc.publisher | Kathmandu University | |
| dc.subject | Estradiol receptors | |
| dc.subject | Fibromatosis | |
| dc.subject | Mesenteric mass | |
| dc.subject | Wide surgical excision | |
| dc.title | Mesenteric Fibromatosis | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 345 | |
| oaire.citation.startPage | 344 | |
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