Abstract
Congenital-Infantile Fibrosarcoma (CIF) is a malignant mesenchymal tumor representing 10-20% of soft-tissue tumors. Complete surgical resection is generally the treatment of choice. The most recurrent cytogenetic abnormality was identified as the traslocation t(12;15)(p13:q25), which bears the fusion of Tel gene EVT6 with TrkC gene. This study describes a case of infantile fibrosarcoma of the ileum in a female newborn examined for intestinal occlusion and its laparoscopic treatment.
| Original language | Italian |
|---|---|
| Pages (from-to) | 173-176 |
| Number of pages | 4 |
| Journal | Pediatria Medica e Chirurgica |
| Volume | 36 |
| Issue number | 4 |
| Publication status | Published - 2014 |
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ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Surgery
Cite this
Trattamento trans-ombelicale video assistito di un fibrosarcoma ileale. / Scirè, G.; Mantovani, A.; Zampieri, Nicola; Guerriero, V.; Segala, D.; Pecori, S.; Bruno, C.; Camoglio, F. S.
In: Pediatria Medica e Chirurgica, Vol. 36, No. 4, 2014, p. 173-176.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Trattamento trans-ombelicale video assistito di un fibrosarcoma ileale
AU - Scirè, G.
AU - Mantovani, A.
AU - Zampieri, Nicola
AU - Guerriero, V.
AU - Segala, D.
AU - Pecori, S.
AU - Bruno, C.
AU - Camoglio, F. S.
PY - 2014
Y1 - 2014
N2 - Congenital-Infantile Fibrosarcoma (CIF) is a malignant mesenchymal tumor representing 10-20% of soft-tissue tumors. Complete surgical resection is generally the treatment of choice. The most recurrent cytogenetic abnormality was identified as the traslocation t(12;15)(p13:q25), which bears the fusion of Tel gene EVT6 with TrkC gene. This study describes a case of infantile fibrosarcoma of the ileum in a female newborn examined for intestinal occlusion and its laparoscopic treatment.
AB - Congenital-Infantile Fibrosarcoma (CIF) is a malignant mesenchymal tumor representing 10-20% of soft-tissue tumors. Complete surgical resection is generally the treatment of choice. The most recurrent cytogenetic abnormality was identified as the traslocation t(12;15)(p13:q25), which bears the fusion of Tel gene EVT6 with TrkC gene. This study describes a case of infantile fibrosarcoma of the ileum in a female newborn examined for intestinal occlusion and its laparoscopic treatment.
KW - Congenital fibrosarcoma
KW - Genetic translocation
KW - Intestinal neonatal occlusion
KW - Laparoscopic treatment
UR - http://www.scopus.com/inward/record.url?scp=84994813266&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84994813266&partnerID=8YFLogxK
M3 - Articolo
VL - 36
SP - 173
EP - 176
JO - Pediatria Medica e Chirurgica
JF - Pediatria Medica e Chirurgica
SN - 0391-5387
IS - 4
ER -