Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare Tumors
Congenital tumors are rare and, owing to this rarity, there is limited information on many of them. A total of 839 fetal and postnatal MRI studies performed in the first 3 months of life were retrospectively reviewed. They were performed with the use of 1.5 T scanners. Seventy-six tumors were diagno...
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MDPI AG
2023-12-01
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Series: | Cancers |
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Online Access: | https://www.mdpi.com/2072-6694/16/1/43 |
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author | Piotr Kwasniewicz Julia Wieczorek-Pastusiak Anna Romaniuk-Doroszewska Monika Bekiesinska-Figatowska |
author_facet | Piotr Kwasniewicz Julia Wieczorek-Pastusiak Anna Romaniuk-Doroszewska Monika Bekiesinska-Figatowska |
author_sort | Piotr Kwasniewicz |
collection | DOAJ |
description | Congenital tumors are rare and, owing to this rarity, there is limited information on many of them. A total of 839 fetal and postnatal MRI studies performed in the first 3 months of life were retrospectively reviewed. They were performed with the use of 1.5 T scanners. Seventy-six tumors were diagnosed based on fetal MRI between 20 and 37 gestational weeks, and 27 were found after birth, from 1 day of age to 3 months of life. Teratomas were the most common tumors in our dataset, mainly in the sacrococcygeal region (SCT), followed by cardiac rhabdomyomas and subependymal giant cell astrocytomas (SEGA) associated with TSC, and neuroblastomas. The group of less common tumors consisted of infantile fibrosarcomas, malignant rhabdoid tumors, mesoblastic nephromas and Wilms tumor, craniopharyngiomas, brain stem gliomas, desmoplastic infantile astrocytoma, choroid plexus carcinoma, glioblastoma, hemangiopericytoma, rhabdomyosarcoma, melanoma, mesenchymal hamartomas of the chest wall and the liver, and juvenile xanthogranuloma, with special consideration of blue rubber bleb nevus syndrome. MRI plays a significant role in further and better characterization of congenital tumors, leading to a correct diagnosis in many cases, which is crucial for pregnancy and neonatal management and psychological preparation of the parents. No diagnosis is impossible and can be absolutely excluded. |
first_indexed | 2024-03-08T15:10:40Z |
format | Article |
id | doaj.art-b97716ba682b47c182c4b78e270d0935 |
institution | Directory Open Access Journal |
issn | 2072-6694 |
language | English |
last_indexed | 2024-03-08T15:10:40Z |
publishDate | 2023-12-01 |
publisher | MDPI AG |
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series | Cancers |
spelling | doaj.art-b97716ba682b47c182c4b78e270d09352024-01-10T14:52:24ZengMDPI AGCancers2072-66942023-12-011614310.3390/cancers16010043Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare TumorsPiotr Kwasniewicz0Julia Wieczorek-Pastusiak1Anna Romaniuk-Doroszewska2Monika Bekiesinska-Figatowska3Department of Diagnostic Imaging, Institute of Mother and Child, 01-211 Warsaw, PolandDepartment of Diagnostic Imaging, Institute of Mother and Child, 01-211 Warsaw, PolandDepartment of Diagnostic Imaging, Institute of Mother and Child, 01-211 Warsaw, PolandDepartment of Diagnostic Imaging, Institute of Mother and Child, 01-211 Warsaw, PolandCongenital tumors are rare and, owing to this rarity, there is limited information on many of them. A total of 839 fetal and postnatal MRI studies performed in the first 3 months of life were retrospectively reviewed. They were performed with the use of 1.5 T scanners. Seventy-six tumors were diagnosed based on fetal MRI between 20 and 37 gestational weeks, and 27 were found after birth, from 1 day of age to 3 months of life. Teratomas were the most common tumors in our dataset, mainly in the sacrococcygeal region (SCT), followed by cardiac rhabdomyomas and subependymal giant cell astrocytomas (SEGA) associated with TSC, and neuroblastomas. The group of less common tumors consisted of infantile fibrosarcomas, malignant rhabdoid tumors, mesoblastic nephromas and Wilms tumor, craniopharyngiomas, brain stem gliomas, desmoplastic infantile astrocytoma, choroid plexus carcinoma, glioblastoma, hemangiopericytoma, rhabdomyosarcoma, melanoma, mesenchymal hamartomas of the chest wall and the liver, and juvenile xanthogranuloma, with special consideration of blue rubber bleb nevus syndrome. MRI plays a significant role in further and better characterization of congenital tumors, leading to a correct diagnosis in many cases, which is crucial for pregnancy and neonatal management and psychological preparation of the parents. No diagnosis is impossible and can be absolutely excluded.https://www.mdpi.com/2072-6694/16/1/43fetusinfantcongenital tumormagnetic resonance imaging (MRI) |
spellingShingle | Piotr Kwasniewicz Julia Wieczorek-Pastusiak Anna Romaniuk-Doroszewska Monika Bekiesinska-Figatowska Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare Tumors Cancers fetus infant congenital tumor magnetic resonance imaging (MRI) |
title | Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare Tumors |
title_full | Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare Tumors |
title_fullStr | Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare Tumors |
title_full_unstemmed | Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare Tumors |
title_short | Congenital Tumors—Magnetic Resonance Imaging Findings with Focus on Rare Tumors |
title_sort | congenital tumors magnetic resonance imaging findings with focus on rare tumors |
topic | fetus infant congenital tumor magnetic resonance imaging (MRI) |
url | https://www.mdpi.com/2072-6694/16/1/43 |
work_keys_str_mv | AT piotrkwasniewicz congenitaltumorsmagneticresonanceimagingfindingswithfocusonraretumors AT juliawieczorekpastusiak congenitaltumorsmagneticresonanceimagingfindingswithfocusonraretumors AT annaromaniukdoroszewska congenitaltumorsmagneticresonanceimagingfindingswithfocusonraretumors AT monikabekiesinskafigatowska congenitaltumorsmagneticresonanceimagingfindingswithfocusonraretumors |