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SHR Neuro Krebs Kardio Lipid

Kaiser, M; Liegl-Atzwanger, B; Nagy, E; Sperl, D; Singer, G; Till, H.
Congenital Infantile Fibrosarcoma Causing Intestinal Perforation in a Newborn.
Case Rep Pediatr. 2017; 2017(1):2969473-2969473 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Autor/innen der Med Uni Graz:
Eibisberger Margarita
Liegl-Atzwanger Bernadette
Nagy Eszter
Singer Georg
Sperl Daniela
Till Holger
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Abstract:
Congenital infantile fibrosarcoma (CIF) is a rare malignant mesenchymal tumor and only 14 cases have been reported with gastrointestinal manifestation. We report about a female newborn delivered per emergency cesarean section at 34 weeks of gestation. Postnatally, she rapidly developed an acute abdomen and sonographic evidence of intestinal perforation requiring laparotomy on the first day of life. A perforated 2 × 3 cm sized spherical tumorous structure of the jejunum was identified. Due to unknown histopathology at this point and unclear resectional margins, she received a temporary ileostomy, which was closed two months later. Histopathology revealed a congenital intestinal fibrosarcoma without the characteristic ETV6-NTRK3 fusion transcript. In conclusion, this rare tumor must be considered as differential diagnosis of intestinal perforations in newborns.

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