Small intestinal submucosal lipoma: a rare cause of secondary intussusception in a child
Background Intestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small intestine occur mainly in elderly patients and seldom occur in childhood. They are frequently asymptomatic, possibly due to their slow growth. These...
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| Published in: | Annals of pediatric surgery Vol. 17; no. 1; pp. 47 - 5 |
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| Main Authors: | , , , , , , , |
| Format: | Journal Article |
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02-08-2021
Springer Nature B.V SpringerOpen |
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| Abstract | Background
Intestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small intestine occur mainly in elderly patients and seldom occur in childhood. They are frequently asymptomatic, possibly due to their slow growth. These tumors may act as a lead point of intussusception.
Case presentation
We report a rare case of double compounded ileo-ileal intussusception due to a submucosal intestinal lipoma in an 8-year-old female. To our knowledge, this is only the seventh pediatric case to be reported in the medical literature.
Conclusions
Small intestinal submucosal lipoma should be considered in case of intussusception in pediatric patients. Surgical resection seems sufficient in case of symptomatic intestinal lipoma with low morbidity. |
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| AbstractList | BackgroundIntestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small intestine occur mainly in elderly patients and seldom occur in childhood. They are frequently asymptomatic, possibly due to their slow growth. These tumors may act as a lead point of intussusception.Case presentationWe report a rare case of double compounded ileo-ileal intussusception due to a submucosal intestinal lipoma in an 8-year-old female. To our knowledge, this is only the seventh pediatric case to be reported in the medical literature.ConclusionsSmall intestinal submucosal lipoma should be considered in case of intussusception in pediatric patients. Surgical resection seems sufficient in case of symptomatic intestinal lipoma with low morbidity. Abstract Background Intestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small intestine occur mainly in elderly patients and seldom occur in childhood. They are frequently asymptomatic, possibly due to their slow growth. These tumors may act as a lead point of intussusception. Case presentation We report a rare case of double compounded ileo-ileal intussusception due to a submucosal intestinal lipoma in an 8-year-old female. To our knowledge, this is only the seventh pediatric case to be reported in the medical literature. Conclusions Small intestinal submucosal lipoma should be considered in case of intussusception in pediatric patients. Surgical resection seems sufficient in case of symptomatic intestinal lipoma with low morbidity. Background Intestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small intestine occur mainly in elderly patients and seldom occur in childhood. They are frequently asymptomatic, possibly due to their slow growth. These tumors may act as a lead point of intussusception. Case presentation We report a rare case of double compounded ileo-ileal intussusception due to a submucosal intestinal lipoma in an 8-year-old female. To our knowledge, this is only the seventh pediatric case to be reported in the medical literature. Conclusions Small intestinal submucosal lipoma should be considered in case of intussusception in pediatric patients. Surgical resection seems sufficient in case of symptomatic intestinal lipoma with low morbidity. |
| ArticleNumber | 47 |
| Author | Zitouni, Hayet Boudawara, Tahya Sellami Cheikhrouhou, Taycir Dhaw, Mahdi Ben Zouari, Mohamed Mhiri, Riadh Gouiaa, Naourez Kallel, Rim |
| Author_xml | – sequence: 1 givenname: Taycir orcidid: 0000-0001-5945-0266 surname: Cheikhrouhou fullname: Cheikhrouhou, Taycir email: cheikhrouhoutaycir@gmail.com organization: Department of Pediatric Surgery, Hedi Chaker Hospital, University of Medicine of Sfax, University of Sfax – sequence: 2 givenname: Mahdi Ben surname: Dhaw fullname: Dhaw, Mahdi Ben organization: Department of Pediatric Surgery, Hedi Chaker Hospital, University of Medicine of Sfax, University of Sfax – sequence: 3 givenname: Mohamed surname: Zouari fullname: Zouari, Mohamed organization: Department of Pediatric Surgery, Hedi Chaker Hospital, University of Medicine of Sfax, University of Sfax – sequence: 4 givenname: Hayet surname: Zitouni fullname: Zitouni, Hayet organization: Department of Pediatric Surgery, Hedi Chaker Hospital, University of Medicine of Sfax, University of Sfax – sequence: 5 givenname: Rim surname: Kallel fullname: Kallel, Rim organization: University of Medicine of Sfax, University of Sfax, Department of Pathology, Habib Bourguiba Hospital – sequence: 6 givenname: Naourez surname: Gouiaa fullname: Gouiaa, Naourez organization: University of Medicine of Sfax, University of Sfax, Department of Pathology, Habib Bourguiba Hospital – sequence: 7 givenname: Tahya Sellami surname: Boudawara fullname: Boudawara, Tahya Sellami organization: University of Medicine of Sfax, University of Sfax, Department of Pathology, Habib Bourguiba Hospital – sequence: 8 givenname: Riadh surname: Mhiri fullname: Mhiri, Riadh organization: Department of Pediatric Surgery, Hedi Chaker Hospital, University of Medicine of Sfax, University of Sfax |
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fullname: NB Ackerman – volume: 57 start-page: 88 year: 2019 ident: 114_CR18 publication-title: Int J Surg Case Rep. doi: 10.1016/j.ijscr.2019.03.003 contributor: fullname: SM Abdelmohsen – volume: 5 start-page: 49 issue: 1 year: 2012 ident: 114_CR11 publication-title: Mac J Med Sci. doi: 10.3889/MJMS.1857-5773.2012.0199 contributor: fullname: V Janevska – ident: 114_CR21 doi: 10.1155/2015/856030 – volume: 42 start-page: 682 issue: 3 year: 2018 ident: 114_CR20 publication-title: World J Surg. doi: 10.1007/s00268-017-4196-z contributor: fullname: HL Tan – volume: 21 start-page: 590 issue: 8 year: 1991 ident: 114_CR15 publication-title: Pediatr Radiol. doi: 10.1007/BF02012606 contributor: fullname: FP McGrath – volume: 23 start-page: 261 issue: 3 year: 2007 ident: 114_CR19 publication-title: Pediatr Surg Int. doi: 10.1007/s00383-006-1838-x contributor: fullname: N Simanovsky |
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| Snippet | Background
Intestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small... BackgroundIntestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small intestine... Abstract Background Intestinal lipomas are benign, non-epithelial, intestinal tumors with an exceptionally rare localization at the ileum. Lipomas in the small... |
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| SubjectTerms | Abdomen Case report Case Reports Child Intestinal obstruction Intussusception Laparotomy Lipoma Literature reviews Males Medical imaging Medicine Medicine & Public Health Older people Pain Pediatrics Small bowel Small intestine Surgery Tomography Tumors Ultrasonic imaging Vomiting |
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| Title | Small intestinal submucosal lipoma: a rare cause of secondary intussusception in a child |
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