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.
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Authors | Alessandro Sandri, Andrea Domenco Manazza, Daniele Bertin, Margherita Silengo, Maria Eleonora Basso, Marco Forni, Enrico Madon |
Journal | Journal of pediatric hematology/oncology
(J Pediatr Hematol Oncol)
Vol. 25
Issue 7
Pg. 558-61
(Jul 2003)
ISSN: 1077-4114 [Print] United States |
PMID | 12847324
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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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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