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Primary mature adrenal teratoma in infant

Teratomas are neoplasms of the embryonic tissues that typically arise in the gonadal and sacrococcygeal regions. Primary adrenal teratoma are extremely rare and only few cases were published in literature. Teratomas contain more than one embryonic germ cell layer, mostly elements derived from ectode...

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Autores principales: Haddad, Siham El, Hessissen, Laila, Kababri, Maria El, Lamalmi, Najat, Kisra, Mounir, Allali, Nazik, Chat, Latifa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532853/
https://www.ncbi.nlm.nih.gov/pubmed/33062128
http://dx.doi.org/10.11604/pamj.2020.37.27.24016
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author Haddad, Siham El
Hessissen, Laila
Kababri, Maria El
Lamalmi, Najat
Kisra, Mounir
Allali, Nazik
Chat, Latifa
author_facet Haddad, Siham El
Hessissen, Laila
Kababri, Maria El
Lamalmi, Najat
Kisra, Mounir
Allali, Nazik
Chat, Latifa
author_sort Haddad, Siham El
collection PubMed
description Teratomas are neoplasms of the embryonic tissues that typically arise in the gonadal and sacrococcygeal regions. Primary adrenal teratoma are extremely rare and only few cases were published in literature. Teratomas contain more than one embryonic germ cell layer, mostly elements derived from ectoderm and least frequently from endoderm. Though these tumors are mostly benign, malignant transformation may occur. Treatment includes surgical removal. We report a rare case of a primary mature retroperitoneal teratoma in an infant with liver metastasis. Imaging modality CT and MRI were useful in diagnosis. The diagnostic and therapeutic challenges of dealing with such a case have been discussed and the literature reviewed.
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spelling pubmed-75328532020-10-13 Primary mature adrenal teratoma in infant Haddad, Siham El Hessissen, Laila Kababri, Maria El Lamalmi, Najat Kisra, Mounir Allali, Nazik Chat, Latifa Pan Afr Med J Case Report Teratomas are neoplasms of the embryonic tissues that typically arise in the gonadal and sacrococcygeal regions. Primary adrenal teratoma are extremely rare and only few cases were published in literature. Teratomas contain more than one embryonic germ cell layer, mostly elements derived from ectoderm and least frequently from endoderm. Though these tumors are mostly benign, malignant transformation may occur. Treatment includes surgical removal. We report a rare case of a primary mature retroperitoneal teratoma in an infant with liver metastasis. Imaging modality CT and MRI were useful in diagnosis. The diagnostic and therapeutic challenges of dealing with such a case have been discussed and the literature reviewed. The African Field Epidemiology Network 2020-09-07 /pmc/articles/PMC7532853/ /pubmed/33062128 http://dx.doi.org/10.11604/pamj.2020.37.27.24016 Text en Copyright: Siham El Haddad et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Haddad, Siham El
Hessissen, Laila
Kababri, Maria El
Lamalmi, Najat
Kisra, Mounir
Allali, Nazik
Chat, Latifa
Primary mature adrenal teratoma in infant
title Primary mature adrenal teratoma in infant
title_full Primary mature adrenal teratoma in infant
title_fullStr Primary mature adrenal teratoma in infant
title_full_unstemmed Primary mature adrenal teratoma in infant
title_short Primary mature adrenal teratoma in infant
title_sort primary mature adrenal teratoma in infant
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532853/
https://www.ncbi.nlm.nih.gov/pubmed/33062128
http://dx.doi.org/10.11604/pamj.2020.37.27.24016
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