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1.
Rev. argent. dermatol ; 100(2): 81-90, jun. 2019. graf
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1020456

ABSTRACT

RESUMEN: La enfermedad de Paget mamaria es una patología poco común de la mama que tiene una gran importancia por su alta asociación a carcinoma mamario y por requerir de un alto índice de sospecha para arribar a su diagnóstico. Se presenta el caso de una mujer de 65 años de edad, con diagnóstico de enfermedad de Paget mamaria asociada a carcinoma ductal infiltrante de mama izquierda con compromiso ganglionar axilar homolateral. Se realizó la revisión bibliográfica de esta patología, con especial énfasis en la clínica, diagnóstico, estadificación, tratamientoy pronóstico.


ABSTRACT: Paget's disease of the breast is a rare pathology in the breast, however, it is very important because of its high association with mammary carcinoma and because it requires a high index of suspicion. We present the case of a 65-year-old woman with Paget's disease of the breast associated with an infiltrating ductal carcinoma of the left breast with homolateral axillary lymph node involvement. A bibliographic review of this pathology was carried out, with special emphasis on the clinic, diagnosis, staging, treatment and prognosis.

2.
Int J Obes (Lond) ; 33(11): 1235-42, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19721450

ABSTRACT

OBJECTIVE: To identify common loci and potential genetic variants affecting body mass index (BMI, kg m(-2)) in study populations originating from Europe. DESIGN: We combined genome-wide linkage scans of six cohorts from Australia, Denmark, Finland, the Netherlands, Sweden and the United Kingdom with an approximately 10-cM microsatellite marker map. Variance components linkage analysis was carried out with age, sex and country of origin as covariates. SUBJECTS: The GenomEUtwin consortium consists of twin cohorts from eight countries (Australia, Denmark, the Netherlands, Finland, Italy, Norway, Sweden and the United Kingdom) with a total data collection of more than 500,000 monozygotic and dizygotic (DZ) twin pairs. Variance due to early-life events and the environment is reduced within twin pairs, which makes DZ pairs highly valuable for linkage studies of complex traits. This study totaled 4401 European-originated twin families (10,535 individuals) from six countries (Australia, Denmark, the Netherlands, Finland, Sweden and the United Kingdom). RESULTS: We found suggestive evidence for a quantitative trait locus on 3q29 and 7q36 in the combined sample of DZ twins (multipoint logarithm of odds score (MLOD) 2.6 and 2.4, respectively). Two individual cohorts showed strong evidence independently for three additional loci: 16q23 (MLOD=3.7) and 2p24 (MLOD=3.4) in the Dutch cohort and 20q13 (MLOD=3.2) in the Finnish cohort. CONCLUSION: Linkage analysis of the combined data in this large twin cohort study provided evidence for suggestive linkage to BMI. In addition, two cohorts independently provided significant evidence of linkage to three new loci. The results of our study suggest a smaller environmental variance between DZ twins than full siblings, with a corresponding increase in heritability for BMI as well as an increase in linkage signal in well-replicated regions. The results are consistent with the possibility of locus heterogeneity for some genomic regions, and indicate a lack of major common quantitative trait locus variants affecting BMI in European populations.


Subject(s)
Body Mass Index , Chromosomes, Human, Pair 3/genetics , Chromosomes, Human, Pair 7/genetics , Genetic Linkage/genetics , Quantitative Trait Loci/genetics , Twins, Dizygotic/genetics , Adult , Aged , Cohort Studies , Europe , Female , Genetic Predisposition to Disease , Humans , Male , Microsatellite Repeats/genetics , Middle Aged , Twins/genetics , White People/genetics
3.
Int J Obes (Lond) ; 33(1): 75-9, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19030008

ABSTRACT

OBJECTIVE: To further investigate a common variant (rs9939609) in the fat mass- and obesity-associated gene (FTO), which recent genome-wide association studies have shown to be associated with body mass index (BMI) and obesity. DESIGN: We examined the effect of this FTO variant on BMI in 3353 Australian adult male and female twins. RESULTS: The minor A allele of rs9939609 was associated with an increased BMI (P=0.0007). Each additional copy of the A allele was associated with a mean BMI increase of approximately 1.04 kg/m(2) (approximately 3.71 kg). Using variance components decomposition, we estimate that this single-nucleotide polymorphism accounts for approximately 3% of the genetic variance in BMI in our sample (approximately 2% of the total variance). By comparing intrapair variances of monozygotic twins of different genotypes we were able to perform a direct test of gene by environment (G x E) interaction in both sexes and gene by parity (G x P) interaction in women, but no evidence was found for either. CONCLUSIONS: In addition to supporting earlier findings that the rs9939609 variant in the FTO gene is associated with an increased BMI, our results indicate that the associated genetic effect does not interact with environment or parity.


Subject(s)
Obesity/genetics , Polymorphism, Single Nucleotide , Proteins/genetics , Twins/genetics , Adult , Age Factors , Aged , Aged, 80 and over , Alpha-Ketoglutarate-Dependent Dioxygenase FTO , Australia , Body Mass Index , Chi-Square Distribution , Europe/ethnology , Female , Gene Expression , Genetic Predisposition to Disease , Genotype , Homozygote , Humans , Life Style , Likelihood Functions , Male , Middle Aged , Parity , Pregnancy , Sex Factors
4.
Int J Obes (Lond) ; 32(10): 1455-67, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18779828

ABSTRACT

OBJECTIVE: Twin studies are useful for investigating the causes of trait variation between as well as within a population. The goals of the present study were two-fold: First, we aimed to compare the total phenotypic, genetic and environmental variances of height, weight and BMI between Caucasians and East Asians using twins. Secondly, we intended to estimate the extent to which genetic and environmental factors contribute to differences in variability of height, weight and BMI between Caucasians and East Asians. DESIGN: Height and weight data from 3735 Caucasian and 1584 East Asian twin pairs (age: 13-15 years) from Australia, China, Finland, Japan, the Netherlands, South Korea, Taiwan and the United States were used for analyses. Maximum likelihood twin correlations and variance components model-fitting analyses were conducted to fulfill the goals of the present study. RESULTS: The absolute genetic variances for height, weight and BMI were consistently greater in Caucasians than in East Asians with corresponding differences in total variances for all three body measures. In all 80 to 100% of the differences in total variances of height, weight and BMI between the two population groups were associated with genetic differences. CONCLUSION: Height, weight and BMI were more variable in Caucasian than in East Asian adolescents. Genetic variances for these three body measures were also larger in Caucasians than in East Asians. Variance components model-fitting analyses indicated that genetic factors contributed to the difference in variability of height, weight and BMI between the two population groups. Association studies for these body measures should take account of our findings of differences in genetic variances between the two population groups.


Subject(s)
Asian People/genetics , Body Height/genetics , Body Mass Index , Body Weight/genetics , White People/genetics , Adolescent , Female , Humans , Male , Sex Characteristics , Twins, Dizygotic , Twins, Monozygotic
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