475 research outputs found

    Peripheral T-Cell Lymphoma with Aberrant Expression of CD19, CD20, and CD79a: Case Report and Literature Review

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    A case of lymphoma of T-cell derivation with aberrant expression of three B-cell lineage markers (CD19, CD20, and CD79a), which was diagnosed on a left axillary excision, is described. Immunohistochemical studies and flow cytometry analysis demonstrated neoplastic cells expressing CD3, CD19, CD20, and CD79a with absence of CD4, CD8, CD10, CD30, CD34, CD56, CD68, TDT, MPO, PAX-5, and surface immunoglobulin. Gene rearrangement studies performed on paraffin blocks demonstrated monoclonal T-cell receptor gamma chain rearrangement with no evidence of clonal heavy chain rearrangement. The neoplastic cells were negative for Epstein-Barr virus (EBV) or Human Herpes Virus 8 (HHV-8). At the time of diagnosis, the PET scan demonstrated hypermetabolic neoplastic cells involving the left axilla, bilateral internal jugular areas, mediastinum, right hilum, bilateral lungs, and spleen. However, bone marrow biopsy performed for hemolytic anemia revealed normocellular bone marrow with trilineage maturation. The patient had no evidence of immunodeficiency or infection with EBV or HHV-8. This is the first reported case of a mature T-cell lymphoma with aberrant expression of three B-cell lineage markers. The current report also highlights the need for molecular gene rearrangement studies to determine the precise lineage of ambiguous neoplastic clones

    Peripheral T-Cell Lymphoma with Aberrant Expression of CD19, CD20, and CD79a: Case Report and Literature Review

    Get PDF
    A case of lymphoma of T-cell derivation with aberrant expression of three B-cell lineage markers (CD19, CD20, and CD79a), which was diagnosed on a left axillary excision, is described. Immunohistochemical studies and flow cytometry analysis demonstrated neoplastic cells expressing CD3, CD19, CD20, and CD79a with absence of CD4, CD8, CD10, CD30, CD34, CD56, CD68, TDT, MPO, PAX-5, and surface immunoglobulin. Gene rearrangement studies performed on paraffin blocks demonstrated monoclonal T-cell receptor gamma chain rearrangement with no evidence of clonal heavy chain rearrangement. The neoplastic cells were negative for Epstein-Barr virus (EBV) or Human Herpes Virus 8 (HHV-8). At the time of diagnosis, the PET scan demonstrated hypermetabolic neoplastic cells involving the left axilla, bilateral internal jugular areas, mediastinum, right hilum, bilateral lungs, and spleen. However, bone marrow biopsy performed for hemolytic anemia revealed normocellular bone marrow with trilineage maturation. The patient had no evidence of immunodeficiency or infection with EBV or HHV-8. This is the first reported case of a mature T-cell lymphoma with aberrant expression of three B-cell lineage markers. The current report also highlights the need for molecular gene rearrangement studies to determine the precise lineage of ambiguous neoplastic clones

    Research Knowledge of Advanced Standing and Traditional Students: Implications for BSW Education

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    The advanced standing model of social work education, which affords graduate credit to qualified BSW students who pursue their MSW, has not been without issue or controversy, including questions of potential differences in performance on various educational outcomes. Specifically related to research curriculum, the importance of which is often not wholly embraced by students, this article reports the results of a secondary data analysis comparing research knowledge among advanced standing and traditional MSW students as well as among the various undergraduate majors (i.e., BSW, psychology, and sociology). Results suggest that research knowledge is similar and low across student subgroups. Important differences in research knowledge were found among student groups based on undergraduate major, with BSW undergraduates without advanced standing, on average, scoring lower than any other group. Implications for BSW research curriculum are considere

    A Noninvasive Method to Detect Mexican Wolves and Estimate Abundance

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    Monitoring wolf abundance is important for recovery efforts of Mexican wolves (Canis lupus baileyi) in the Blue Range Wolf Recovery Area in Arizona and New Mexico, USA. Although radiotelemetry has been a reliable method, collaring and tracking wolves in an expanding population will be prohibitively expensive and alternative methods to estimate abundance will become necessary. We applied 10 canid microsatellite loci to 235 Mexican wolf samples, 48 coyote (C. latrans) samples, and 14 domestic dog (C. lupus familiaris) samples to identify alleles that provide reliable separation of these species. We then evaluated an approach for prescreening, noninvasively collected DNA obtained from fecal samples to identify Mexican wolves. We generated complete genotypes for only those samples identified as probable Mexican wolves. We used these genotypes to estimate mark–recapture population estimates of Mexican wolves and compared these to known numbers of wolves in the study area.We collected fecal samples during 3 sampling periods in 2007–2008 and used Huggins-type mark–recapture models to estimate Mexican wolf abundance. We were able to generate abundance estimates with 95% confidence for 2 of 3 sampling periods. We estimated abundance to be 10 (95% Cl = 6–34) during one sampling period when the known abundance was 10 and we estimated abundance to be 9 (95% CI = 6 –30) during the other sampling period when the known abundance was 10. The application of this noninvasive method to estimate Mexican wolf abundance provides an alternative monitoring tool that could be useful for long-term monitoring of this and other recovering populations. Published 2016. This article is a U.S. Government work and is in the public domain in the USA

    A Noninvasive Method to Detect Mexican Wolves and Estimate Abundance

    Get PDF
    Monitoring wolf abundance is important for recovery efforts of Mexican wolves (Canis lupus baileyi) in the Blue Range Wolf Recovery Area in Arizona and New Mexico, USA. Although radiotelemetry has been a reliable method, collaring and tracking wolves in an expanding population will be prohibitively expensive and alternative methods to estimate abundance will become necessary. We applied 10 canid microsatellite loci to 235 Mexican wolf samples, 48 coyote (C. latrans) samples, and 14 domestic dog (C. lupus familiaris) samples to identify alleles that provide reliable separation of these species. We then evaluated an approach for prescreening, noninvasively collected DNA obtained from fecal samples to identify Mexican wolves. We generated complete genotypes for only those samples identified as probable Mexican wolves. We used these genotypes to estimate mark–recapture population estimates of Mexican wolves and compared these to known numbers of wolves in the study area.We collected fecal samples during 3 sampling periods in 2007–2008 and used Huggins-type mark–recapture models to estimate Mexican wolf abundance. We were able to generate abundance estimates with 95% confidence for 2 of 3 sampling periods. We estimated abundance to be 10 (95% Cl = 6–34) during one sampling period when the known abundance was 10 and we estimated abundance to be 9 (95% CI = 6 –30) during the other sampling period when the known abundance was 10. The application of this noninvasive method to estimate Mexican wolf abundance provides an alternative monitoring tool that could be useful for long-term monitoring of this and other recovering populations. Published 2016. This article is a U.S. Government work and is in the public domain in the USA

    Brief for the United States as Amicus Curiae in Support of Neither Party

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    Amicus ("friend of the court") brief written by the United States in support of petitioners in AMP v. Myriad Genetics (Supreme Court Case Docket No. 12-398)

    Gallbladder Cancer Incidence Among American Indians and Alaska Natives, US, 1999–2004

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    BACKGROUND. Gallbladder cancer (GBC) is rare; however, it disproportionately affects the American Indian and Alaska Natives (AI/AN) population. The purpose of the study was to characterize GBC among AI/AN in the US population. METHODS. Cases of GBC diagnosed between 1999 and 2004 and collected by state-based cancer registries were included. Registry records were linked with Indian Health Service (IHS) administration records to decrease race misclassification of AI/AN. GBC rates and/or percent distributions for AI/AN and non-Hispanic whites (NHW) were calculated by sex, IHS region, age, and stage for all US counties and IHS Contract Health Service Delivery Area (CHSDA) counties, in which approximately 56% of US AI/AN individuals reside. RESULTS. In CHSDA counties, the GBC incidence rate among AI/AN was 3.3 per 100,000, which was significantly higher than that among NHW (P \u3c .05). Rates varied widely among IHS regions and ranged from 1.5 in the East to 5.5 in Alaska. Rates were higher among AI/AN females than males in all regions, except the Northern Plains. Higher percentages of GBC were diagnosed among AI/AN aged CONCLUSIONS. To the authors’ knowledge to date, this is the most comprehensive study of GBC incidence among AI/AN in the US. The accurate characterization of GBC in this population could help inform the development of interventions aimed at reducing morbidity and mortality from this diseas

    Associations of somatic depressive symptoms with food attentional bias and eating behaviors

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    Recent evidence suggests that atypical major depressive disorder (MDD) – whose key features include the reversed somatic symptoms of hyperphagia (increased appetite) and hypersomnia (increased sleep) – is a stronger predictor of future obesity than other MDD subtypes. The mechanisms underlying this relationship are unclear. The present study sought to elucidate whether the individual symptoms of hyperphagia, hypersomnia, poor appetite, and disturbed sleep have differential relationships with food attentional bias, emotional eating, external eating, and restrained eating. This cross-sectional laboratory study involved 103 young adults without obesity (mean age = 20 years, 79% female, 26% non-White, mean BMI = 23.4 kg/m2). We measured total depressive symptom severity and individual symptoms of hyperphagia, poor appetite, and disturbed sleep using the Hopkins Symptom Checklist-20 (SCL-20) and added an item to assess hypersomnia; food attentional bias using a Food Stroop task; and self-reported eating behaviors using the Dutch Eating Behavior Questionnaire. Hyperphagia was positively associated with emotional eating but negatively associated with food attentional bias. Hypersomnia was negatively associated with emotional eating. Poor appetite was negatively associated with emotional eating. Disturbed sleep was positively associated with food attentional bias and emotional eating. An aggregate of the remaining 15 depressive symptoms (SCL-15) was positively associated with emotional and restrained eating. Our findings highlight the importance of examining the direction of somatic depressive symptoms, and they set the stage for future research to identify subgroups of people with depression at greatest risk for obesity (e.g., those with hyperphagia and/or disturbed sleep) and the mechanisms responsible for this elevated risk (e.g., emotional eating)
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