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Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report

Superior mediastinal syndrome secondary to an anterior mediastinal mass can be seen in acute lymphoblastic leukaemia (ALL) of T-cell lineage. We report a 3-year-old child with B-cell ALL, who presented with the superior mediastinal syndrome. The CT scan chest showed a huge anterior mediastinal mass...

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Autores principales: Rahat-Ul-Ain, Faizan, Mahwish, Fatima, Saba, Mehmood, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666274/
https://www.ncbi.nlm.nih.gov/pubmed/36405934
http://dx.doi.org/10.3332/ecancer.2022.1457
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author Rahat-Ul-Ain,
Faizan, Mahwish
Fatima, Saba
Mehmood, Khalid
author_facet Rahat-Ul-Ain,
Faizan, Mahwish
Fatima, Saba
Mehmood, Khalid
author_sort Rahat-Ul-Ain,
collection PubMed
description Superior mediastinal syndrome secondary to an anterior mediastinal mass can be seen in acute lymphoblastic leukaemia (ALL) of T-cell lineage. We report a 3-year-old child with B-cell ALL, who presented with the superior mediastinal syndrome. The CT scan chest showed a huge anterior mediastinal mass and the peripheral blood immunophenotyping showed B-cell ALL. High-risk remission induction chemotherapy was given and he achieved remission by the end of induction therapy, both in terms of medullary and extramedullary disease, and is on maintenance chemotherapy now. This is the first reported case of a paediatric B-cell ALL presenting with superior mediastinal syndrome secondary to an anterior mediastinal mass.
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spelling pubmed-96662742022-11-18 Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report Rahat-Ul-Ain, Faizan, Mahwish Fatima, Saba Mehmood, Khalid Ecancermedicalscience Case Report Superior mediastinal syndrome secondary to an anterior mediastinal mass can be seen in acute lymphoblastic leukaemia (ALL) of T-cell lineage. We report a 3-year-old child with B-cell ALL, who presented with the superior mediastinal syndrome. The CT scan chest showed a huge anterior mediastinal mass and the peripheral blood immunophenotyping showed B-cell ALL. High-risk remission induction chemotherapy was given and he achieved remission by the end of induction therapy, both in terms of medullary and extramedullary disease, and is on maintenance chemotherapy now. This is the first reported case of a paediatric B-cell ALL presenting with superior mediastinal syndrome secondary to an anterior mediastinal mass. Cancer Intelligence 2022-10-31 /pmc/articles/PMC9666274/ /pubmed/36405934 http://dx.doi.org/10.3332/ecancer.2022.1457 Text en © the authors; licensee ecancermedicalscience. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (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
Rahat-Ul-Ain,
Faizan, Mahwish
Fatima, Saba
Mehmood, Khalid
Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report
title Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report
title_full Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report
title_fullStr Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report
title_full_unstemmed Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report
title_short Superior mediastinal syndrome in paediatric B-cell acute lymphoblastic leukaemia: a case report
title_sort superior mediastinal syndrome in paediatric b-cell acute lymphoblastic leukaemia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666274/
https://www.ncbi.nlm.nih.gov/pubmed/36405934
http://dx.doi.org/10.3332/ecancer.2022.1457
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