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A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports
Desmoplastic infantile astrocytomas (DIAs), are rare supratentorial tumors, usually observed in the first 24 months of life. Despite their aggressive appearance, they tend to follow a favorable clinical course. Total or near total resection of tumor is usually the treatment option. Desmoplastic Infa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315091/ https://www.ncbi.nlm.nih.gov/pubmed/32595403 http://dx.doi.org/10.14744/SEMB.2018.29292 |
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author | Tanık, Canan Devecioğlu, Elif Gökçe Hasçiçek, Seyhan Meltem Can, Songül Halefoğlu, Ahmet Mesrur Kabukçuoğlu, Fevziye |
author_facet | Tanık, Canan Devecioğlu, Elif Gökçe Hasçiçek, Seyhan Meltem Can, Songül Halefoğlu, Ahmet Mesrur Kabukçuoğlu, Fevziye |
author_sort | Tanık, Canan |
collection | PubMed |
description | Desmoplastic infantile astrocytomas (DIAs), are rare supratentorial tumors, usually observed in the first 24 months of life. Despite their aggressive appearance, they tend to follow a favorable clinical course. Total or near total resection of tumor is usually the treatment option. Desmoplastic Infantile Ganglioglioma (DIG) and DIA are WHO grade I tumors that have similar clinical and morphological findings. The only criterion in differential diagnosis is the neural component of DIG. These tumors both have dense fibroblastic stroma and positive staining with glial fibrillar acidic protein (GFAP) and CD34. A rare case of desmoplastic infantile astrocytoma presenting with right side partial seizures presented in a 1-year-old child. A rare case of desmoplastic infantile astrocytoma presenting with focal onset generalized seizures presented in a 1-year-old child. Despite their radiological and histological properties, these tumors have a benign course. After 3-year follow-up for the first case and 1-year follow-up for the second case, there was no recurrence. |
format | Online Article Text |
id | pubmed-7315091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-73150912020-06-25 A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports Tanık, Canan Devecioğlu, Elif Gökçe Hasçiçek, Seyhan Meltem Can, Songül Halefoğlu, Ahmet Mesrur Kabukçuoğlu, Fevziye Sisli Etfal Hastan Tip Bul Case Report Desmoplastic infantile astrocytomas (DIAs), are rare supratentorial tumors, usually observed in the first 24 months of life. Despite their aggressive appearance, they tend to follow a favorable clinical course. Total or near total resection of tumor is usually the treatment option. Desmoplastic Infantile Ganglioglioma (DIG) and DIA are WHO grade I tumors that have similar clinical and morphological findings. The only criterion in differential diagnosis is the neural component of DIG. These tumors both have dense fibroblastic stroma and positive staining with glial fibrillar acidic protein (GFAP) and CD34. A rare case of desmoplastic infantile astrocytoma presenting with right side partial seizures presented in a 1-year-old child. A rare case of desmoplastic infantile astrocytoma presenting with focal onset generalized seizures presented in a 1-year-old child. Despite their radiological and histological properties, these tumors have a benign course. After 3-year follow-up for the first case and 1-year follow-up for the second case, there was no recurrence. Kare Publishing 2018-09-28 /pmc/articles/PMC7315091/ /pubmed/32595403 http://dx.doi.org/10.14744/SEMB.2018.29292 Text en Copyright: © 2018 by The Medical Bulletin of Sisli Etfal Hospital http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/). |
spellingShingle | Case Report Tanık, Canan Devecioğlu, Elif Gökçe Hasçiçek, Seyhan Meltem Can, Songül Halefoğlu, Ahmet Mesrur Kabukçuoğlu, Fevziye A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports |
title | A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports |
title_full | A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports |
title_fullStr | A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports |
title_full_unstemmed | A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports |
title_short | A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports |
title_sort | rare tumor in childhood desmoplastic infantile astrocytoma: two case reports |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315091/ https://www.ncbi.nlm.nih.gov/pubmed/32595403 http://dx.doi.org/10.14744/SEMB.2018.29292 |
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