ID 110221
Title Transcription
ショウチョウカンマク デスモイド シュヨウ ノ 1レイ
Title Alternative
A case of mesenteric desmoid tumor
Author
Yuasa, Yasuhiro Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital
Okitsu, Hiroshi Department of Surgery, Tokushima Red Cross Hospital
Inoue, Seiya Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital Tokushima University Educator and Researcher Directory
Yamai, Hiromichi Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital
Yoshida, Takahiro Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Takechi, Hirokazu Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Seike, Junichi Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital
Honda, Junko Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital
Tangoku, Akira Department of Esophageal, Breast and Thyroid Surgery, Tokushima University Hospital Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Keywords
mesenteric tumor
desmoid tumor
intra-abdominal desmoid
Content Type
Journal Article
Description
A 51-year-old man was referred to our hospital in 2005, because of an abdominal mass in thehypogastrium. There was no tenderness, and the tumor moved to epigastric resion easily. Therewere no important findings in a physical examination, except the mass. Enhanced CT showed themass with clear boundaries of 8cm size that the inside was contrasted heterogeneously in pelviccavity, and the internal was able to confirm tessellated mass by a supersonic wave. We doubtedintestinal GIST and performed an operation. We showed mass of mesoileum origin, in 15cm oralside from terminal ileum, there was no adhesion and invasion to circumference, so we underwent apartial resection of the terminal ileum. It was diagnosed as desmoid of a mesoileum origin by apostoperative histopathology diagnosis. There has been no recurrence for postoperative threeyears. Intraabdominal desmoid is relatively rare, and often noted a history of the laparotomy orestrogenic intervention, and combined with Gardner’s syndrome. In addition, it is assumed that itusually grows infiltrative, and easy to develop local recurrence. We experienced a rare case fallingunder neither, so we report it.
Journal Title
四国医学雑誌
ISSN
00373699
NCID
AN00102041
Publisher
徳島医学会
Volume
64
Issue
1-2
Start Page
31
End Page
34
Sort Key
31
Published Date
2008-04-25
FullText File
language
jpn
TextVersion
Publisher
departments
Medical Sciences
University Hospital