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1.
PLoS One ; 10(3): e0121107, 2015.
Article in English | MEDLINE | ID: mdl-25815726

ABSTRACT

UNLABELLED: Despite complex presentation of adult hypertension and a concomitant obesity epidemic, little is known about overweight in relation to blood pressure among Caribbean children. We examined blood pressure in relation to body size in a cross-sectional study of 573 Barbadian children aged 9-10 years (2010-2011). The United States normative blood pressure percentiles were used to identify children with high (≥95th percentile) or high normal blood pressure (90th-95th percentile). The World Health Organization body mass index cut-off points were used to assess weight status. MAJOR FINDINGS: Thirty percent of children were overweight/obese. Percentage fat mass differed between girls (20.4%) and boys (17.72%) (p<0.05). Mean systolic blood pressure among girls was 106.11 (95% CI 105.05, 107.17) mmHg and 105.23 (104.09, 106.38) for boys. The percentages with high or high-normal mean systolic blood pressure were 14.38% (10.47, 18.29) for girls and 8.08% (4.74, 11.41) for boys. Height and body mass index were independent correlates of systolic and diastolic blood pressure. Mean systolic blood pressure was related to lean mass but not fat mass, while diastolic blood pressure was associated with fat mass index and overweight. PRINCIPAL CONCLUSION: One third of 9-10 year old children in Barbados were overweight/obese and 12% had elevated mean systolic blood pressure. BP was related to body size. These findings signal potential adverse trends in weight gain and BP trends for children growing up in the context of a country that has recently undergone rapid economic transition.


Subject(s)
Blood Pressure/physiology , Body Composition/physiology , Hypertension/epidemiology , Overweight/epidemiology , Barbados , Body Mass Index , Caribbean Region , Child , Female , Humans , Hypertension/physiopathology , Male , Overweight/physiopathology
2.
Ann Diagn Pathol ; 9(6): 330-4, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16308163

ABSTRACT

We report the first pediatric case of malignant pigmented epithelioid clear-cell tumor arising from kidney; the lesion occurred in a 12-year-old girl without tuberous sclerosis. The tumor was widely metastatic to the retroperitoneum and chest, and the patient died of the disease 9 months after diagnosis, despite active chemotherapy. Pigmented epithelioid clear-cell tumor of the kidney is a rare variant of epithelioid angiomyolipoma and a member of the family of perivascular epithelioid cell tumors (PEComas). The tumor demonstrated overlapping features between clear-cell sugar tumor and epithelioid variant of angiomyolipoma. Tumor cells were positive for HMB-45 expression, negative for any evidence of muscular differentiation, and contained melanin pigment and premelanosomes in the cytoplasm. Diffuse C-Kit (CD117) positivity was identified throughout the tumor. This is the first report of C-Kit-positive malignant PEComas.


Subject(s)
Angiomyolipoma/metabolism , Kidney Neoplasms/metabolism , Proto-Oncogene Proteins c-kit/metabolism , Angiomyolipoma/diagnosis , Angiomyolipoma/pathology , Child , Female , Humans , Kidney Neoplasms/diagnosis , Kidney Neoplasms/pathology , Retroperitoneal Neoplasms/pathology , Retroperitoneal Neoplasms/secondary , Thoracic Neoplasms/pathology , Thoracic Neoplasms/secondary , Tuberous Sclerosis
3.
Arch Neurol ; 60(5): 767-70, 2003 May.
Article in English | MEDLINE | ID: mdl-12756143

ABSTRACT

BACKGROUND: The determination of the form of prion disease and early diagnosis are important for prognostic, public health, and epidemiologic reasons. OBJECTIVE: To describe a patient with sporadic Creutzfeldt-Jakob disease (sCJD) who had a clinical history and initial electroencephalogram and magnetic resonance imaging findings consistent with variant CJD (vCJD). RESULTS: Results of a repeated electroencephalogram were suggestive of sCJD, and a subsequent brain biopsy confirmed this diagnosis. CONCLUSIONS: This case cautions against relying solely on T2- and diffusion-weighted pulvinar hyperintensity and clinical features to differentiate between vCJD and sCJD, and further supports established diagnostic criteria for vCJD.


Subject(s)
Creutzfeldt-Jakob Syndrome/pathology , Magnetic Resonance Imaging , Adult , Biopsy , Brain/pathology , Creutzfeldt-Jakob Syndrome/classification , Diagnosis, Differential , Electroencephalography , Female , Humans , Pulvinar/pathology
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