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Metachronic Breast and Cerebellar Neoplasm in a Young Patient
Several factors trigger the development of genetic mutations that are responsible for causing a neoplasm. Medulloblastoma is a malignant and invasive cerebellar neoplasm, that affects children and young adults. Mucinous carcinoma is a special type of breast cancer. Being a special atypical subtype o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Revinter Publicações Ltda
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316863/ https://www.ncbi.nlm.nih.gov/pubmed/32227327 http://dx.doi.org/10.1055/s-0040-1701456 |
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author | Nascimento, Jéssika de Oliveira Haro, Lara Caroline Anastacio Sá, Rafael da Silva Storch, Rebeca Espelho |
author_facet | Nascimento, Jéssika de Oliveira Haro, Lara Caroline Anastacio Sá, Rafael da Silva Storch, Rebeca Espelho |
author_sort | Nascimento, Jéssika de Oliveira |
collection | PubMed |
description | Several factors trigger the development of genetic mutations that are responsible for causing a neoplasm. Medulloblastoma is a malignant and invasive cerebellar neoplasm, that affects children and young adults. Mucinous carcinoma is a special type of breast cancer. Being a special atypical subtype of invasive carcinoma, it most frequently affects women of advanced age and represents 1 to 7% of all breast cancers. The reported case aims to show the rarity of the occurrence of desmoplastic medulloblastoma and mammary mucinous carcinoma in a young patient in a short period of time, in different sites, without direct anatomical attachment and without occurrence of metastasis. Initially, this patient had a desmoplastic medulloblastoma and was treated with lumpectomy and radiotherapy. After 13 months, the patient was diagnosed with a mucinous breast carcinoma, underwent mastectomy, adjuvant chemotherapy and is currently undergoing endocrinotherapy. We conclude, based on the metachronous characteristic of the neoplasia and clinical characteristics, that the patient is likely to have Li-Fraumeni syndrome, an autosomal dominant disease with mutation of the TP53 gene, which is the the main involved. Because the patient does not present all the characteristics of the phenotype of the syndrome, she can thus be classified as having Li-Fraumeni variant or Li-Fraumeni-like syndrome. |
format | Online Article Text |
id | pubmed-10316863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Thieme Revinter Publicações Ltda |
record_format | MEDLINE/PubMed |
spelling | pubmed-103168632023-07-27 Metachronic Breast and Cerebellar Neoplasm in a Young Patient Nascimento, Jéssika de Oliveira Haro, Lara Caroline Anastacio Sá, Rafael da Silva Storch, Rebeca Espelho Rev Bras Ginecol Obstet Several factors trigger the development of genetic mutations that are responsible for causing a neoplasm. Medulloblastoma is a malignant and invasive cerebellar neoplasm, that affects children and young adults. Mucinous carcinoma is a special type of breast cancer. Being a special atypical subtype of invasive carcinoma, it most frequently affects women of advanced age and represents 1 to 7% of all breast cancers. The reported case aims to show the rarity of the occurrence of desmoplastic medulloblastoma and mammary mucinous carcinoma in a young patient in a short period of time, in different sites, without direct anatomical attachment and without occurrence of metastasis. Initially, this patient had a desmoplastic medulloblastoma and was treated with lumpectomy and radiotherapy. After 13 months, the patient was diagnosed with a mucinous breast carcinoma, underwent mastectomy, adjuvant chemotherapy and is currently undergoing endocrinotherapy. We conclude, based on the metachronous characteristic of the neoplasia and clinical characteristics, that the patient is likely to have Li-Fraumeni syndrome, an autosomal dominant disease with mutation of the TP53 gene, which is the the main involved. Because the patient does not present all the characteristics of the phenotype of the syndrome, she can thus be classified as having Li-Fraumeni variant or Li-Fraumeni-like syndrome. Thieme Revinter Publicações Ltda 2020-02 /pmc/articles/PMC10316863/ /pubmed/32227327 http://dx.doi.org/10.1055/s-0040-1701456 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nascimento, Jéssika de Oliveira Haro, Lara Caroline Anastacio Sá, Rafael da Silva Storch, Rebeca Espelho Metachronic Breast and Cerebellar Neoplasm in a Young Patient |
title | Metachronic Breast and Cerebellar Neoplasm in a Young Patient |
title_full | Metachronic Breast and Cerebellar Neoplasm in a Young Patient |
title_fullStr | Metachronic Breast and Cerebellar Neoplasm in a Young Patient |
title_full_unstemmed | Metachronic Breast and Cerebellar Neoplasm in a Young Patient |
title_short | Metachronic Breast and Cerebellar Neoplasm in a Young Patient |
title_sort | metachronic breast and cerebellar neoplasm in a young patient |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316863/ https://www.ncbi.nlm.nih.gov/pubmed/32227327 http://dx.doi.org/10.1055/s-0040-1701456 |
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