Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter

Schinzel-Giedion syndrome which is associated with midfacial hypoplasia and coarse dysmorphic features is a multiple congenital malformation syndrome. It is believed that risk of malignancy may be a component of the anomaly. We report herein a case of a 16 months old boy with SGS associated with sac...

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Detalles Bibliográficos
Autores principales: Anyanwu, Lofty-John, Mohammad, Aminu, Muhammad, Habeeb, Aliyu, Ibrahim, Abdullahi, Lawal, Farinyaro, Aliyu, Iya, Abdulkarim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398236/
https://www.ncbi.nlm.nih.gov/pubmed/28451008
http://dx.doi.org/10.11604/pamj.2017.26.30.11525
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author Anyanwu, Lofty-John
Mohammad, Aminu
Muhammad, Habeeb
Aliyu, Ibrahim
Abdullahi, Lawal
Farinyaro, Aliyu
Iya, Abdulkarim
author_facet Anyanwu, Lofty-John
Mohammad, Aminu
Muhammad, Habeeb
Aliyu, Ibrahim
Abdullahi, Lawal
Farinyaro, Aliyu
Iya, Abdulkarim
author_sort Anyanwu, Lofty-John
collection PubMed
description Schinzel-Giedion syndrome which is associated with midfacial hypoplasia and coarse dysmorphic features is a multiple congenital malformation syndrome. It is believed that risk of malignancy may be a component of the anomaly. We report herein a case of a 16 months old boy with SGS associated with sacrococcygeal teratoma and cor-triatriatum dexter. Histopathology report of the excised sacrococcygeal mass showed no malignant foci. He was however lost to follow up in the second week post-operation.
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spelling pubmed-53982362017-04-27 Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter Anyanwu, Lofty-John Mohammad, Aminu Muhammad, Habeeb Aliyu, Ibrahim Abdullahi, Lawal Farinyaro, Aliyu Iya, Abdulkarim Pan Afr Med J Case Report Schinzel-Giedion syndrome which is associated with midfacial hypoplasia and coarse dysmorphic features is a multiple congenital malformation syndrome. It is believed that risk of malignancy may be a component of the anomaly. We report herein a case of a 16 months old boy with SGS associated with sacrococcygeal teratoma and cor-triatriatum dexter. Histopathology report of the excised sacrococcygeal mass showed no malignant foci. He was however lost to follow up in the second week post-operation. The African Field Epidemiology Network 2017-01-23 /pmc/articles/PMC5398236/ /pubmed/28451008 http://dx.doi.org/10.11604/pamj.2017.26.30.11525 Text en © Lofty-John Anyanwu et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Anyanwu, Lofty-John
Mohammad, Aminu
Muhammad, Habeeb
Aliyu, Ibrahim
Abdullahi, Lawal
Farinyaro, Aliyu
Iya, Abdulkarim
Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter
title Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter
title_full Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter
title_fullStr Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter
title_full_unstemmed Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter
title_short Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter
title_sort schinzel-giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398236/
https://www.ncbi.nlm.nih.gov/pubmed/28451008
http://dx.doi.org/10.11604/pamj.2017.26.30.11525
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