Literature DB >> 12469263

Congenital solitary intestinal fibromatosis.

A Numanoglu1, J Davies, A J W Millar, H Rode.   

Abstract

Neonatal intestinal obstruction due to a tumour is rare. We report a six-day-old male neonate who presented with abdominal distension and vomiting. Laparotomy revealed colonic obstruction caused by a stenosing fibrotic lesion in the proximal transverse colon. Histopathological examination of the resected specimen confirmed fibromatosis. We believe this represents the third reported case of solitary colonic fibromatosis. The literature on neonatal intestinal fibromatosis is reviewed.

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Year:  2002        PMID: 12469263     DOI: 10.1055/s-2002-35957

Source DB:  PubMed          Journal:  Eur J Pediatr Surg        ISSN: 0939-7248            Impact factor:   2.191


  5 in total

1.  Desmoid tumour (aggressive fibromatosis) of the colon mimics malignancy on dual time-point 18F-FDG PET/CT imaging.

Authors:  W Makis; A Ciarallo; G Abikhzer; J Stern; J Laufer
Journal:  Br J Radiol       Date:  2012-02       Impact factor: 3.039

2.  Colorectal infantile myofibromatosis: an unusual cause of rectal prolapse and sigmoid colo-colonic intussusception: a case report.

Authors:  Deepti Dhall; Philip K Frykman; Hanlin L Wang
Journal:  Cases J       Date:  2008-12-15

3.  Primary colonic congenital infantile fibrosarcoma presenting as meconium peritonitis.

Authors:  Saleem Islam; Oliver S Soldes; Robert Ruiz; James D Geiger
Journal:  Pediatr Surg Int       Date:  2008-02-05       Impact factor: 1.827

4.  A Solitary Intestinal Myofibroma: A Rare Cause of Neonatal Anemia.

Authors:  Janna S E Ottenhoff; Peter G J Nikkels; C E J Terwisscha van Scheltinga; L Naeije
Journal:  Case Rep Oncol       Date:  2017-10-17

5.  Solitary intestinal myofibroma an unusual cause of neonatal intestinal obstruction.

Authors:  Hussain Al Eid; Hussain Abusrair; Faedah Almowasher; Ryadh Nasrullah; Mohammed Alkhater; Zahra Almarhoon
Journal:  Ann Saudi Med       Date:  2014 Nov-Dec       Impact factor: 1.526

  5 in total

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