Coexistence of duodenum derived aggressive fibromatosis and paraduodenal hydatid cyst: A case report and review of literature

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dc.authoridYILMAZ, Mehmet/0000-0002-5710-5263
dc.authoridAlan, Saadet/0000-0003-2329-151X
dc.authoridYilmaz, Sezai/0000-0002-8044-0297
dc.authoridAkbulut, Sami/0000-0002-6864-7711
dc.authorwosidYILMAZ, Mehmet/HKM-4739-2023
dc.authorwosidYilmaz, Mehmet/AAF-6095-2021
dc.authorwosidAlan, Saadet/ABH-4282-2020
dc.authorwosidYilmaz, Sezai/ABI-2323-2020
dc.authorwosidAkbulut, Sami/L-9568-2014
dc.contributor.authorAkbulut, Sami
dc.contributor.authorYilmaz, Mehmet
dc.contributor.authorAlan, Saadet
dc.contributor.authorKolu, Mehmet
dc.contributor.authorKaradag, Nese
dc.date.accessioned2024-08-04T20:57:26Z
dc.date.available2024-08-04T20:57:26Z
dc.date.issued2018
dc.departmentİnönü Üniversitesien_US
dc.description.abstractIntra-abdominal aggressive fibromatosis is a locally aggressive tumor mostly originating from the mesentery or retroperitoneal space, infiltrating adjacent tissues, and very rarely metastasizing to distant organs. There are only two case reports in the English language literature where intra-abdominal aggressive fibromatosis originated from the intestinal wall. In this study, we aimed to report a case of aggressive fibromatosis originating from the muscularis propria layer of the duodenum and invading pancreas. Another interesting aspect of this case is that a primary paraduodenal hydatid cyst was incidentally detected in the surgical specimen. A 46-year-old female patient presented to our clinic with postprandial nausea and vomiting. A contrast-enhanced abdominal computerized tomography revealed a mass lesion with a size of 100 mm x 80 mm which originated from the distal pancreas and compressed the gastric pilor externally. Upon exploration the distal part of duodenum, proximal jejunum, and pancreatic mass were noted to form a conglomerated structure. Therefore, the fourth part of the duodenum, a 25 cm part of the proximal jejunum, distal pancreas, and the spleen were excised en-bloc. The pathology report of the specimen indicated fibromatosis with a diameter of 55 mm that originated from the muscularis propria of the duodenum and extended into the pancreatic parenchyma. There was also an incidentally detected 10 mm paraduodenal hydatid cyst. No tumor recurrence was detected at a follow-up period of 24 mo. In conclusion, the most ideal treatment of desmoid-type fibromatosis is surgical resection of the mass lesion with clean surgical borders. Although rare, this tumor may originate from the intestinal wall. Histopathological verification is of great significance for a proper diagnosis.en_US
dc.identifier.doi10.4240/wjgs.v10.i8.90
dc.identifier.endpage94en_US
dc.identifier.issn1948-9366
dc.identifier.issue8en_US
dc.identifier.pmid30510634en_US
dc.identifier.startpage90en_US
dc.identifier.urihttps://doi.org/10.4240/wjgs.v10.i8.90
dc.identifier.urihttps://hdl.handle.net/11616/102616
dc.identifier.volume10en_US
dc.identifier.wosWOS:000451408000002en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherBaishideng Publishing Group Incen_US
dc.relation.ispartofWorld Journal of Gastrointestinal Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDuodenal wallen_US
dc.subjectHydatid cysten_US
dc.subjectAggressive fibromatosisen_US
dc.subjectIntra-abdominal fibromatosisen_US
dc.subjectDesmoid tumoren_US
dc.subjectDesmoid-type fibromatosisen_US
dc.titleCoexistence of duodenum derived aggressive fibromatosis and paraduodenal hydatid cyst: A case report and review of literatureen_US
dc.typeReview Articleen_US

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