A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS
Case report: Chromosomal breakage syndromes are characterized by cancer predisposition. Here we present a 27-month-old female with Fanconi Aplastic Anemia diagnosed with 4 tumors. Imaging showed brain mass causing the shift, liver mass and left kidney mass. She had diagnosed with high grade intracra...
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Elsevier
2021
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oai:doaj.org-article:f930ca1d0d7b4c71971ffe85a9798bfd2021-11-10T04:39:20ZA CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS2531-137910.1016/j.htct.2021.10.1099https://doaj.org/article/f930ca1d0d7b4c71971ffe85a9798bfd2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2531137921012463https://doaj.org/toc/2531-1379Case report: Chromosomal breakage syndromes are characterized by cancer predisposition. Here we present a 27-month-old female with Fanconi Aplastic Anemia diagnosed with 4 tumors. Imaging showed brain mass causing the shift, liver mass and left kidney mass. She had diagnosed with high grade intracranial tm, wilms tm and hepatocellular ca. Because of refractory pancitopeni, she underwent HSCT. After 2months she developed intracranial embryonal tumor. The patient died with progression. Genetic tests revealed no mutation.Fatma Tuba YILDIRIMDerya ÖZYÖRÜKArzu YAZAL ERDEMSelma ÇAKMAKCINeriman SARISonay İNCESOYİnci İLHANElsevierarticleDiseases of the blood and blood-forming organsRC633-647.5ENHematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S65- (2021) |
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Diseases of the blood and blood-forming organs RC633-647.5 |
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Diseases of the blood and blood-forming organs RC633-647.5 Fatma Tuba YILDIRIM Derya ÖZYÖRÜK Arzu YAZAL ERDEM Selma ÇAKMAKCI Neriman SARI Sonay İNCESOY İnci İLHAN A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS |
description |
Case report: Chromosomal breakage syndromes are characterized by cancer predisposition. Here we present a 27-month-old female with Fanconi Aplastic Anemia diagnosed with 4 tumors. Imaging showed brain mass causing the shift, liver mass and left kidney mass. She had diagnosed with high grade intracranial tm, wilms tm and hepatocellular ca. Because of refractory pancitopeni, she underwent HSCT. After 2months she developed intracranial embryonal tumor. The patient died with progression. Genetic tests revealed no mutation. |
format |
article |
author |
Fatma Tuba YILDIRIM Derya ÖZYÖRÜK Arzu YAZAL ERDEM Selma ÇAKMAKCI Neriman SARI Sonay İNCESOY İnci İLHAN |
author_facet |
Fatma Tuba YILDIRIM Derya ÖZYÖRÜK Arzu YAZAL ERDEM Selma ÇAKMAKCI Neriman SARI Sonay İNCESOY İnci İLHAN |
author_sort |
Fatma Tuba YILDIRIM |
title |
A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS |
title_short |
A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS |
title_full |
A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS |
title_fullStr |
A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS |
title_full_unstemmed |
A CASE DIAGNOSED WITH FOUR DIFFERENT TUMORS |
title_sort |
case diagnosed with four different tumors |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/f930ca1d0d7b4c71971ffe85a9798bfd |
work_keys_str_mv |
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_version_ |
1718440615143800832 |