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Schinzel-Giedion syndrome with sacrococcygeal teratoma.

Abstract
A case of Schinzel-Giedion syndrome, a rare malformation syndrome, is described. In addition to the classic features of the syndrome, the patient had a malignant sacrococcygeal teratoma and agenesis of the corpus callosum. So far, this patient is the fifth case with a sacrococcygeal tumor and the eighth with anomalies of the corpus callosum. According to this occurrence of uncommon tumors, risk of malignancy could be a component of Schinzel-Giedion syndrome.
AuthorsAlessandro Sandri, Andrea Domenco Manazza, Daniele Bertin, Margherita Silengo, Maria Eleonora Basso, Marco Forni, Enrico Madon
JournalJournal of pediatric hematology/oncology (J Pediatr Hematol Oncol) Vol. 25 Issue 7 Pg. 558-61 (Jul 2003) ISSN: 1077-4114 [Print] United States
PMID12847324 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • alpha-Fetoproteins
Topics
  • Abnormalities, Multiple (diagnosis, pathology)
  • Endodermal Sinus Tumor (pathology, surgery)
  • Fatal Outcome
  • Female
  • Humans
  • Infant
  • Male
  • Sacrococcygeal Region
  • Teratoma (diagnosis, pathology, surgery)
  • alpha-Fetoproteins (analysis)

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