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Título
Caracterización clínica y molecular del cáncer de mama en varón
Autor(es)
Director(es)
Palabras clave
Oncology
Cáncer
Oncología
Caracterización clínica
Caracterización molecular
Cancer
Fecha de publicación
2017
Resumen
[ES] El cáncer de mama en varón es una entidad poco frecuente y poco caracterizada y en la
clínica habitual se considera a efectos de tratamiento y pronóstico como el cáncer de
mama en mujer.
Para saber más sobre esta entidad, nos hemos propuesto realizar un estudio descriptivo
del cáncer de mama en varón en nuestro entorno. Para ello hemos revisado las historias
clínicas de 46 pacientes diagnosticados de cáncer de mama en la Unidad de Consejo
Genético de Cáncer Hereditario del Centro de Investigación del Cáncer, y hemos
estudiado los genes BRCA1 y BRCA2 de dichos pacientes mediante secuenciación
masiva.
El 48% de los pacientes tenía antecedentes de cáncer de mama, y el 93% de los pacientes
fueron diagnosticados de carcinoma ductal infiltrante. El 23% de los pacientes
presentaron un grado de proliferación tumoral bajo, mientras que el 77% presentaron un
grado de proliferación medio-alto. Todos los pacientes padecían un carcinoma de mama
subtipo luminal, siendo el 55% de ellos luminal A y el 45% restante luminal B. En el 21%
de los pacientes se hallaron mutaciones en los genes BRCA, siendo el 86% de ellas
mutaciones patogénicas en BRCA2 y el 14% restante variantes de significado incierto en
BRCA1.
Los pacientes con CMV de nuestra área geográfica son similares a los de otras zonas; sin
embargo, presentan mayor grado de proliferación tumoral y mayor expresión de
receptores hormonales que el cáncer de mama en mujer. Asimismo, parece ser que las
formas familiares en varones están más ligadas a BRCA2 que sus homólogas en mujeres.Breast cancer in men is a rare and poorly characterized entity and in the
Usual clinic is considered for treatment and prognostic purposes as the cancer of
mother in woman.
To find out more about this entity, we have undertaken a descriptive study
of male breast cancer in our environment. To this end, we have reviewed the stories
clinics of 46 patients diagnosed with breast cancer in the Counseling Unit
Hereditary Cancer Genetic Center for Cancer Research, and we have
studied the BRCA1 and BRCA2 genes of these patients by sequencing
massive.
48% of patients had a history of breast cancer, and 93% of patients
were diagnosed with infiltrating ductal carcinoma. 23% of patients
The tumour proliferation rate was low, while 77% showed a low level of
medium-high proliferation rate. All the patients suffered from breast carcinoma
luminal subtype, 55% of them luminal A and the remaining 45% luminal B. In 21% of the cases
of the patients, mutations were found in the BRCA genes, 86% of whom were
pathogenic mutations in BRCA2 and the remaining 14% variants of uncertain significance in
BRCA1.
CMV patients in our geographic area are similar to those in other areas; without
However, they have a higher degree of tumor proliferation and greater expression of
hormone receptors than breast cancer in women. It also appears that the
Familial forms in males are more closely linked to BRCA2 than their female counterparts.Breast cancer in men is a rare and poorly characterized entity and in the
Usual clinic is considered for treatment and prognostic purposes as the cancer of
mother in woman.
To find out more about this entity, we have undertaken a descriptive study
of male breast cancer in our environment. To this end, we have reviewed the stories
clinics of 46 patients diagnosed with breast cancer in the Counseling Unit
Hereditary Cancer Genetic Center for Cancer Research, and we have
studied the BRCA1 and BRCA2 genes of these patients by sequencing
massive.
48% of patients had a history of breast cancer, and 93% of patients
were diagnosed with infiltrating ductal carcinoma. 23% of patients
The tumour proliferation rate was low, while 77% showed a low level of
medium-high proliferation rate. All the patients suffered from breast carcinoma
luminal subtype, 55% of them luminal A and the remaining 45% luminal B. In 21% of the cases
of the patients, mutations were found in the BRCA genes, 86% of whom were
pathogenic mutations in BRCA2 and the remaining 14% variants of uncertain significance in
BRCA1.
CMV patients in our geographic area are similar to those in other areas; without
However, they have a higher degree of tumor proliferation and greater expression of
hormone receptors than breast cancer in women. It also appears that the
Familial forms in males are more closely linked to BRCA2 than their female counterparts.
Descripción
Trabajo de fin de grado. Grado en Medicina. Curso académico 2016-2017
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