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1.
Mol Biol Evol ; 41(7)2024 Jul 03.
Article in English | MEDLINE | ID: mdl-38982580

ABSTRACT

South American coca (Erythroxylum coca and E. novogranatense) has been a keystone crop for many Andean and Amazonian communities for at least 8,000 years. However, over the last half-century, global demand for its alkaloid cocaine has driven intensive agriculture of this plant and placed it in the center of armed conflict and deforestation. To monitor the changing landscape of coca plantations, the United Nations Office on Drugs and Crime collects annual data on their areas of cultivation. However, attempts to delineate areas in which different varieties are grown have failed due to limitations around identification. In the absence of flowers, identification relies on leaf morphology, yet the extent to which this is reflected in taxonomy is uncertain. Here, we analyze the consistency of the current naming system of coca and its four closest wild relatives (the "coca clade"), using morphometrics, phylogenomics, molecular clocks, and population genomics. We include name-bearing type specimens of coca's closest wild relatives E. gracilipes and E. cataractarum. Morphometrics of 342 digitized herbarium specimens show that leaf shape and size fail to reliably discriminate between species and varieties. However, the statistical analyses illuminate that rounder and more obovate leaves of certain varieties could be associated with the subtle domestication syndrome of coca. Our phylogenomic data indicate extensive gene flow involving E. gracilipes which, combined with morphometrics, supports E. gracilipes being retained as a single species. Establishing a robust evolutionary-taxonomic framework for the coca clade will facilitate the development of cost-effective genotyping methods to support reliable identification.


Subject(s)
Phylogeny , Biological Evolution , Coca/genetics , Plant Leaves/anatomy & histology , Plant Leaves/genetics
2.
J Trop Pediatr ; 68(5)2022 08 04.
Article in English | MEDLINE | ID: mdl-36130307

ABSTRACT

Hemoglobin S is caused by a nucleotide change in HBB gene (HBB:c.20A>T, p.Glu6Val), is presented in diverse forms: simple carriers (HbSA), homozygotes (HbSS) also known as sickle cell anemia, and compound heterozygotes with other ß-hemoglobinopathies. It is worldwide distributed, in Mexico, is frequently observed in the southern states Guerrero, Oaxaca and Chiapas. Elevated fetal hemoglobin (HbF) is associated with mild phenotype; single-nucleotide variants (SNVs) in modifier genes, such as BCL11A, HBG2, HBBP1 pseudogene and HBS1L-MYB intergenic region, upregulate HbF synthesis. The aim of this study was to identify HbF regulating genetic variants in HbSS and HbSA Mexican subjects. We studied 39 individuals (HbSS = 24, 61%, HbSA = 15, 39%) from Chiapas (67%) and Guerrero (33%), peripheral blood was collected in ethylenediamine tetraacetic acid (EDTA) for molecular and hematological studies, DNA was isolated by salting-out technic and genotyping was performed through allelic discrimination by real time polymerase chain reaction (RT-PCR) using Taqman® probes for 15 SNV (in BCL11A: rs6706648, rs7557939, rs4671393, rs11886868, rs766432, rs7599488, rs1427407; HBS1L-MYB: rs28384513, rs7776054, rs9399137, rs4895441, rs9402686, rs1320963; HBG2: rs7482144; and HBBP1: rs10128556). The obtained data were analyzed using IMB SPSS v.22.0 software. All minor alleles were observed in frequencies over 0.05, the most frequent was rs9402686 (0.82), while the less frequent was rs101028556 (0.08). In HbSS group, the mean fetal hemoglobin was 11.9 ± 5.9% and was significantly elevated in BCL11A rs11886868 wildtype homozygotes and in carriers of HBS1L-MYB intergenic region rs7776054 (p = 0.04 and p = 0.03, respectively). In conclusion, in HbSS Mexican patients, two SNVs were observed related to increased HbF; BCL11A rs11886868 and HBS1L-MYB rs7776054.


Sickle cell anemia (SCA) is one of the most common types of hemoglobinopathies in people of African ancestry, it is caused by homozygosity of HbS mutation (HBB:c.20A>T). It is known that fetal hemoglobin plays a key role in decreasing HbS polymerization which damages the erythrocyte structure and is responsible for the characteristic hemolytic crises endured by these patients. Single-nucleotide variant (SNV) in genes that regulate fetal hemoglobin (HbF) after birth have been associated with its increment, thus ameliorating the hematologic phenotype of this pathology and other ß-hemoglobinopathies. Therefore, in this study, we identified, for the first time in Mexican patients with SCA (HbSS) and HbS carriers (HbSA), the presence of 15 SNVs on BCL11A, HBS1L-MYB and HBG2; all HbSS patients had anemia and elevated HbF; 2 variants were related to increased HbF rs11688888C of BCL11A and rs7776054G of HBSIL-MYB; and finally, all minor alleles were found at a frequency higher than 0.05.


Subject(s)
Anemia, Sickle Cell , Fetal Hemoglobin , DNA, Intergenic , Edetic Acid , Fetal Hemoglobin/genetics , Hemoglobin, Sickle/genetics , Heterozygote , Homozygote , Humans , Mexico , Nucleotides , Polymorphism, Single Nucleotide , Repressor Proteins/genetics
3.
Soc Psychiatry Psychiatr Epidemiol ; 57(12): 2457-2468, 2022 Dec.
Article in English | MEDLINE | ID: mdl-35633398

ABSTRACT

PURPOSE: Mental health conditions may affect outcome of COVID-19 disease, while exposure to stressors during the pandemic may impact mental health. The purpose of this study was to examine these factors in relation to ocurrence of depression and anxiety after the first outbreak in Spain. METHODS: We contacted 9515 participants from a population-based cohort study in Catalonia between May and October 2020. We drew blood samples to establish infection to the virus. Pre-pandemic mental health conditions were confirmed through Electronic Health Registries. We used the Hospital Anxiety and Depression Scale to assess severe depression and anxiety post-pandemic. Exposure to proximal, financial and wider environment stressors during the lockdown were collected. We calculated Relative Risks (RR), adjusting for individual- and contextual covariates. RESULTS: Pre-pandemic mental health disorders were not associated with SARS-CoV-2 infection , but were associated with severity of COVID-19 disease. People with pre-existing mental health disorders showed higher prevalence of severe depression (25.4%) and anxiety (37.8%) than those without prior mental disorders (4.9% and 10.1%). Living alone was a strong predictor of severe depression among mental health patients (RR = 1.6, 95% CI 1.2-2.2). Among those without prior mental health disorders, post-lockdown depression and anxiety were associated with household interpersonal conflicts (RR = 2.6, 95% CI 2.1-3.1; RR = 2.1, 95% CI 1.9-2.4) and financial instability (RR = 2.2, 95% CI 1.8-2.9; 1.9, 95% CI 1.6-2.2). CONCLUSIONS: The COVID-19 pandemic and the lockdown were associated with increased post-lockdown depression and anxiety. Patients with pre-existing mental health conditions are a vulnerable group for severe COVID-19 disease.


Subject(s)
COVID-19 , Humans , COVID-19/epidemiology , Pandemics , Mental Health , Spain/epidemiology , SARS-CoV-2 , Cohort Studies , Depression/epidemiology , Depression/psychology , Stress, Psychological/epidemiology , Stress, Psychological/psychology , Communicable Disease Control , Anxiety/epidemiology , Anxiety/psychology
4.
Rev. cir. (Impr.) ; 73(2): 222-226, abr. 2021.
Article in Spanish | LILACS | ID: biblio-1388801

ABSTRACT

Resumen El hiperparatiroidismo primario (HPP) se define como un trastorno endocrinológico caracterizado por hipercalcemia y niveles de hormona paratiroidea (PTH) elevados o inadecuadamente normales resultado de la secreción excesiva de PTH de una o más glándulas paratiroides. Con respecto a la causa, en un 85% se debe a un adenoma paratiroideo único y un 95% de los casos son esporádicos, sin un factor etiológico identificable. La presentación clásica en la mayoría de los casos es de forma asintomática, sin embargo, sus síntomas o signos clásicos incluyen los derivados de la afectación renal, donde la nefrolitiasis es la manifestación clínica más frecuente de la afectación ósea y de la hipercalcemia. El diagnóstico es bioquímico, sin necesidad de estudio imagenológico, el cual se realiza únicamente como pruebas localizadoras prequirúrgicas. El tratamiento definitivo es quirúrgico, siendo la paratiroidectomía con abordaje cervical el procedimiento de elección.


Primary hyperparathyroidism (PHP) is defined as an endocrine disorder characterized by hypercalcemia and elevated or inadequately normal parathyroid hormone (PTH) levels resulting from the excessive secretion of PTH from one or more parathyroid glands. The cause of this disorder is due, in 85%, to a single parathyroid adenoma and most cases (95%) are sporadic, without an identifiable etiologic factor. PHP is asymptomatic in most patients, however, classic symptoms or signs include those derived from renal involvement, where nephrolithiasis is the most frequent clinical manifestation, and those derived from bone affectation and hypercalcemia. The diagnosis is biochemical, without the need for an imaging study, which is performed only as pre-surgical locator tests. The definitive treatment is surgical, being the parathyroidectomy with cervical approach the procedure of choice.


Subject(s)
Humans , Hyperparathyroidism, Primary/diagnosis , Hyperparathyroidism, Primary/etiology , Hyperparathyroidism, Primary/therapy , Diagnosis, Differential , Calcium-Regulating Hormones and Agents/therapeutic use
9.
Mol Neurodegener ; 14(1): 14, 2019 03 27.
Article in English | MEDLINE | ID: mdl-30917850

ABSTRACT

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a multifactorial fatal motoneuron disease without a cure. Ten percent of ALS cases can be pointed to a clear genetic cause, while the remaining 90% is classified as sporadic. Our study was aimed to uncover new connections within the ALS network through a bioinformatic approach, by which we identified C13orf18, recently named Pacer, as a new component of the autophagic machinery and potentially involved in ALS pathogenesis. METHODS: Initially, we identified Pacer using a network-based bioinformatic analysis. Expression of Pacer was then investigated in vivo using spinal cord tissue from two ALS mouse models (SOD1G93A and TDP43A315T) and sporadic ALS patients. Mechanistic studies were performed in cell culture using the mouse motoneuron cell line NSC34. Loss of function of Pacer was achieved by knockdown using short-hairpin constructs. The effect of Pacer repression was investigated in the context of autophagy, SOD1 aggregation, and neuronal death. RESULTS: Using an unbiased network-based approach, we integrated all available ALS data to identify new functional interactions involved in ALS pathogenesis. We found that Pacer associates to an ALS-specific subnetwork composed of components of the autophagy pathway, one of the main cellular processes affected in the disease. Interestingly, we found that Pacer levels are significantly reduced in spinal cord tissue from sporadic ALS patients and in tissues from two ALS mouse models. In vitro, Pacer deficiency lead to impaired autophagy and accumulation of ALS-associated protein aggregates, which correlated with the induction of cell death. CONCLUSIONS: This study, therefore, identifies Pacer as a new regulator of proteostasis associated with ALS pathology.


Subject(s)
Amyotrophic Lateral Sclerosis/metabolism , Amyotrophic Lateral Sclerosis/pathology , Autophagy/drug effects , DNA-Binding Proteins/metabolism , Motor Neurons/metabolism , Amyotrophic Lateral Sclerosis/genetics , Animals , Disease Models, Animal , Humans , Mice, Transgenic , Spinal Cord/metabolism , Spinal Cord/pathology , Superoxide Dismutase/genetics , Superoxide Dismutase/metabolism
10.
Mult Scler Relat Disord ; 28: 117-124, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30593980

ABSTRACT

BACKGROUND: A high percentage of patients with multiple sclerosis present cognitive alterations. Because 4-aminopyridine improves nerve conduction and efficient synaptic connection could improve cognitive dysfunction. OBJECTIVE: To evaluate the efficacy on cognitive performance and safety of 4-aminopyridine administered to patients with relapsing-remitting multiple sclerosis. METHODS: A randomized, double-blind, placebo controlled clinical trial was conducted in patients with relapsing-remitting multiple sclerosis diagnosis according to the McDonald criteria. At the beginning and at the end of the treatment different tests were used to assess cognitive performance. Subsequently, patients were randomized 1:1 to receive treatment or placebo. A bootstrap-t test was proposed to test the effectiveness of cognitive performance, considering a p-value < 0.05 as statistically significant. RESULTS: Twenty-four patients were recruited of which 21 completed the trial, 11 with 4-aminopyridine and 10 with placebo treatment. No significant differences between groups in the initial assessments were observed. In terms of efficacy, the experimental group achieved significantly higher scores in attention span, verbal fluency, planning and graphics and constructive motion. CONCLUSIONS: 4-aminopyridine proved to be an effective treatment on cognitive aspects in patients with relapsing-remitting multiple sclerosis. Drug doses were shown to be safe with mild to moderate adverse events (ClinicalTrials.gov number, NCT02280096).


Subject(s)
4-Aminopyridine/therapeutic use , Attention/drug effects , Executive Function/drug effects , Multiple Sclerosis, Relapsing-Remitting/drug therapy , Multiple Sclerosis, Relapsing-Remitting/psychology , Nootropic Agents/therapeutic use , 4-Aminopyridine/adverse effects , Adult , Disability Evaluation , Double-Blind Method , Female , Humans , Male , Middle Aged , Neuropsychological Tests , Nootropic Agents/adverse effects , Preliminary Data , Treatment Outcome
11.
Rev. fac. cienc. méd. (Impr.) ; 15(1): 10-19, 2018. tab
Article in Spanish | LILACS | ID: biblio-946412

ABSTRACT

Los pacientes diagnosticados con cáncer están en riesgo de malnutrición debido al efecto físico o metabólico de la enfermedad y a las terapias utilizadas en su manejo. La pérdida de peso y la malnutrición, son problemas frecuentes que afectan del 40% al 80% de los pacientes con cáncer, prolongando la estadía hospitalaria, disminuyendo la tolerancia y respuesta a la terapia, encareciendo los costos, afectando la calidad y sobrevida global. Objetivo: evaluar el estado nutricional y el riesgo de desnutrirse en pacientes diagnosticados con cáncer en el Hospital General San Felipe. Material y Métodos: estudio descriptivo, transversal, no aleatorizado, en 100 pacientes oncológicos adultos en los que se determinó los datos generales, sintomatología, hábitos tóxicos, comorbilidades, medidas antropométricas, índice de masa corporal y rendimiento físico. Se aplicó el instrumento de la Valoración Global Subjetiva Generada por el Paciente. Resultados: de los 100 casos estudiados 80 fueron mujeres y 20 hombres, los tipos de cáncer más frecuentes fueron: de mama, genital femenino, esófago-gástrico y colo-rectal; la mayoría presentaron síntomas de impacto nutricional. El uso de alcohol y tabaco fue 18% y 11% respectivamente. La hipertensión arterial y la diabetes mellitus fueron las comorbilidades más frecuentes; 48% presentaron índice de masa corporal en rango normal, 14% bajo peso y 38% sobrepeso. Según la Escala del Grupo Oncológico Cooperativo del Este 47% presentaron estado funcional normal y el 53% se encontró cierto grado de afectación. Al aplicarse el instrumento para Valoración Global Subjetiva, 55% de los 100 casos perdieron peso en los últimos 6 meses y 63% en el último mes. De acuerdo a la escala de reconocimiento físico global 59 pacientes mostraron déficit de peso, la evaluación del tejido graso y muscular mostró déficit en más de la mitad de los casos, 60% de los pacientes estaban moderada a severamente malnutridos y el riesgo de desnutrirse fue del 90%. Conclusión: la condición nutricional está afectada en más de la mitad de los casos y el riesgo de desnutrirse está presente en la mayoría de los pacientes oncológicos.


Subject(s)
Humans , Male , Female , Neoplasms , Nutritional Status , Nutritional Status/radiation effects , Protein-Energy Malnutrition
12.
Acta neurol. colomb ; 33(4): 257-259, oct.-dic. 2017. graf
Article in Spanish | LILACS | ID: biblio-886456

ABSTRACT

RESUMEN Alteraciones autonómicas agudas por infartos cerebrales se han descrito con frecuencia comprometiendo la región insular, dentro de las anormalidades se han documentado alteraciones de severidad variable del ritmo cardíaco, incluyendo la bradicardia extrema sintomática; en la literatura solo hay un reporte de caso de bradi-cardia extrema asociado a un infarto talámico paramediano bilateral, a continuación, describimos un segundo caso de un infarto talámico con la misma presentación.


SUMMARY Acute autonomic disturbances due to cerebral in farcts has been describe frequently with association of the insular cortex, within the describe abnormalities had been document a variety of cardiac disturbances including extreme symptomatic bradycardia; In the literature just exist a case report of extreme bradycardia associate with a bilateral paramedian thalamic infarct, in the following article, we describe a second case of this infarct with the same presentation.


Subject(s)
Thalamic Nuclei , Bradycardia , Cerebral Infarction , Nystagmus, Pathologic
13.
An. pediatr. (2003. Ed. impr.) ; 84(5): e1-e9, mayo 2016. tab, ilus
Article in Spanish | IBECS | ID: ibc-151600

ABSTRACT

El hemocultivo (HC) es el método diagnóstico de elección ante la sospecha de bacteriemia, siendo una de las técnicas microbiológicas más solicitadas en pediatría. Diversos cambios han acontecido en los últimos años como la introducción de nuevas vacunas, el aumento creciente de pacientes portadores de catéteres vasculares centrales, o la irrupción de los sistemas automáticos de procesamiento de los HC. Dichos cambios han propiciado la revisión y la actualización de los distintos aspectos relacionados con esta técnica con el fin de optimizar su uso. Se presenta una guía práctica sobre recomendaciones acerca de la extracción, el procesamiento y la interpretación de los HC elaborada por la Sociedad Española de Urgencias de Pediatría y la Sociedad Española de Infectología Pediátrica. Tras revisar la información científica disponible, se presentan una serie de recomendaciones para cada uno de los siguientes apartados: indicaciones en Urgencias, técnica de extracción, transporte y procesamiento de la muestra, factores a tener en cuenta en situaciones especiales (indicaciones e interpretación de resultados en el paciente inmunodeprimido y/o portador de catéter vascular central, indicaciones de HC para anaerobios), diferenciación entre bacteriemia y contaminación ante un HC con crecimiento bacteriano y actitud a tomar ante un HC positivo en el paciente con fiebre sin foco


Blood culture (BC) is the gold standard when a bacteraemia is suspected, and is one of the most requested microbiological tests in paediatrics. Some changes have occurred in recent years: the introduction of new vaccines, the increasing number of patients with central vascular catheters, as well as the introduction of continuous monitoring BC systems. These changes have led to the review and update of different factors related to this technique in order to optimise its use. A practice guideline is presented with recommendations on BC, established by the Spanish Society of Paediatric Emergency Care and the Spanish Society for Paediatric Infectious Diseases. After reviewing the available scientific evidence, several recommendations for each of the following aspects are presented: BC indications in the Emergency Department, how to obtain, transport and process cultures, special situations (indications and interpretation of results in immunosuppressed patients and/or central vascular catheter carriers, indications for anaerobic BC), differentiation between bacteraemia and contamination when a BC shows bacterial growth and actions to take with a positive BC in patients with fever of unknown origin


Subject(s)
Humans , Male , Female , Infant , Bacteremia/complications , Bacteremia/prevention & control , Bacteremia/therapy , Microbiological Techniques/instrumentation , Microbiological Techniques/methods , Microbiological Techniques , Pediatrics , Fever/diagnosis , Fever/prevention & control , Ambulatory Care/methods , Ambulatory Care , Vaccines/pharmacology , Vaccines/therapeutic use , Practice Guidelines as Topic/standards , Spain
14.
J Fish Biol ; 88(3): 1223-8, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26817438

ABSTRACT

The occurrence of tiger shark Galeocerdo cuvier in the Atlantic Ocean was assessed using at-sea observer data from multiple pelagic longline fisheries. Geographic positions of 2764 G. cuvier recorded between 1992 and 2013 and covering a wide area of the Atlantic Ocean were compared with the currently accepted distribution ranges of the species. Most records fell outside those ranges in both the Southern and Northern Hemispheres, which strongly suggests that the distribution range of G. cuvier in the open ocean is considerably larger than previously described.


Subject(s)
Sharks/physiology , Algorithms , Animals , Atlantic Ocean , Fisheries , Water Movements
15.
An Pediatr (Barc) ; 84(5): 294.e1-9, 2016 May.
Article in Spanish | MEDLINE | ID: mdl-26227314

ABSTRACT

Blood culture (BC) is the gold standard when a bacteraemia is suspected, and is one of the most requested microbiological tests in paediatrics. Some changes have occurred in recent years: the introduction of new vaccines, the increasing number of patients with central vascular catheters, as well as the introduction of continuous monitoring BC systems. These changes have led to the review and update of different factors related to this technique in order to optimise its use. A practice guideline is presented with recommendations on BC, established by the Spanish Society of Paediatric Emergency Care and the Spanish Society for Paediatric Infectious Diseases. After reviewing the available scientific evidence, several recommendations for each of the following aspects are presented: BC indications in the Emergency Department, how to obtain, transport and process cultures, special situations (indications and interpretation of results in immunosuppressed patients and/or central vascular catheter carriers, indications for anaerobic BC), differentiation between bacteraemia and contamination when a BC shows bacterial growth and actions to take with a positive BC in patients with fever of unknown origin.


Subject(s)
Bacteremia/blood , Bacteremia/diagnosis , Blood Culture/standards , Blood Specimen Collection/standards , Child , Decision Trees , Emergency Service, Hospital , Humans
16.
Domest Anim Endocrinol ; 48: 77-83, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24906932

ABSTRACT

Equine pituitary pars intermedia function can be assessed by the measurement of baseline and thyrotropin releasing hormone (TRH)-induced concentrations of adrenocorticotropic hormone (ACTH); however, these measurements may be affected by the environment. Therefore, a prospective observational study evaluated the influence of feeding, time of the day, and season on baseline and TRH-induced concentrations of ACTH in healthy horses. Baseline ACTH was measured in 50 horses before and 2 h after feeding. Six research horses were subjected to a crossover study in which 6 TRH tests were performed in 2 different seasons, March-April (MA) and July-September (JS), at 2 different times of the day, 8 AM and 8 PM, and, under 2 different conditions relative to feeding status, fasted and 2 h after feeding. Differences between fasted and fed horses were found in baseline ACTH, 17.1 ± 1.8 versus 46.1 ± 7.6 pg/mL (P = 0.003) and TRH-stimulated ACTH: 124.1 ± 21.3 versus 192.6 ± 33.1 pg/mL (P = 0.029) at 10 min, and 40.1 ± 4.9 versus 73.2 ± 13.4 pg/mL (P = 0.018) at 30 min post TRH injection. No differences were found between tests performed at different times of the day. Basal ACTH concentrations were greater in JS than in MA, 17.1 ± 1.8 versus 11.9 ± 0.6 pg/mL (P = 0.006). A seasonal influence was also found in stimulated ACTH values, which were much greater in JS 122.7 ± 36.7 versus 31.2 ± 7.4 pg/mL, at 10 min (P = 0.03) and 39.0 ± 7.2 versus 19.8 ± 3.1 pg/mL, at 30 min (P = 0.03). In addition to season, feeding is a potential confounding factor when measuring baseline or stimulated ACTH in horses. In conclusion, feeding status should be standardized for the diagnosis of equine pituitary pars intermedia dysfunction.


Subject(s)
Adrenocorticotropic Hormone/blood , Circadian Rhythm , Food Deprivation , Horses/physiology , Seasons , Thyrotropin-Releasing Hormone/pharmacology , Animals , Europe , Female , Male
17.
Rev Med Suisse ; 10(424): 738, 740-3, 2014 Apr 02.
Article in French | MEDLINE | ID: mdl-24772806

ABSTRACT

Primary cutaneous B-cell lymphomas (PCBCL) present as skin lesions without evidence of extracutaneous involvement at diagnosis. This article summarizes clinical and histopathological features of the three main types of PCBCL: primary cutaneous marginal zone lymphoma, primary cutaneous follicle center lymphoma and primary cutaneous diffuse large B-cell lymphoma, leg type. It will discuss initial staging procedures, necessary to differentiate PCBCL from systemic lymphoma with secondary skin involvement. Finally, we will review the main treatments, local therapy (radiotherapy, surgical excision) for indolent PCBCL and multiagent chemotherapy for primary cutaneous diffuse large B-cell lymphoma, leg type.


Subject(s)
Lymphoma, B-Cell , Skin Neoplasms , Biopsy , Diagnostic Imaging , Humans , Lymphoma, B-Cell/diagnosis , Lymphoma, B-Cell/pathology , Lymphoma, B-Cell/therapy , Molecular Diagnostic Techniques , Neoplasm Staging , Skin Neoplasms/diagnosis , Skin Neoplasms/pathology , Skin Neoplasms/therapy
18.
Rev Med Suisse ; 10(424): 744, 746-8, 2014 Apr 02.
Article in French | MEDLINE | ID: mdl-24772807

ABSTRACT

Follicular lymphoma is an indolent B-cell lymphoma. Fluctuant asymptomatic lymphadenopathies are their usual clinical manifestation. B-cell neoplasms can sometimes involve the skin. In this case, it is important to distinguish a systemic B-cell lymphoma with secondary skin involvement from primary cutaneous lymphoma. Immunohistochemical stainings and staging usually allow to make the difference. Here we report the first case of a systemic follicular lymphoma with secondary cutaneous involvement presented with papular lesions on the face mimicking a rosacea.


Subject(s)
Lymphoma, Follicular/diagnosis , Aged, 80 and over , Biopsy , Diagnosis, Differential , Humans , In Situ Hybridization, Fluorescence , Lymphoma, Follicular/genetics , Lymphoma, Follicular/pathology , Male , Neutrophil Infiltration
19.
Dermatology ; 225(4): 320-5, 2012.
Article in English | MEDLINE | ID: mdl-23257934

ABSTRACT

BACKGROUND: Bullous pemphigoid (BP) is the most common autoimmune blistering skin disease and is associated with an increased mortality. The end points of our study were to evaluate the mortality rate in a retrospective cohort of BP patients followed up to 5 years after the diagnosis and to determine prognostics factors. METHODS: All new cases of BP diagnosed between 1990 and 2003 in the University Hospital of Geneva were retrospectively collected. 60 patients were included, 47 (88.6%) of whom were treated with a combination of corticosteroids and chlorambucil. RESULTS: The 1-year, 2-year and 5-year probabilities of death were 26.7, 37.1 and 60.8%, respectively. Old age, dementia and use of chlorambucil at initial doses of 6 mg/day, but not at lower doses, were associated with poor prognosis in multivariate analysis. CONCLUSION: Our study confirms that BP is associated with a high mortality. The observed mortality rates are however higher than those of previous studies, which is probably related to the inclusion of more debilitated patients.


Subject(s)
Adrenal Cortex Hormones/therapeutic use , Cause of Death , Pemphigoid, Bullous/mortality , Adult , Age Factors , Aged , Aged, 80 and over , Antineoplastic Agents, Alkylating/therapeutic use , Chlorambucil/therapeutic use , Cohort Studies , Dementia/complications , Humans , Middle Aged , Multivariate Analysis , Pemphigoid, Bullous/drug therapy , Retrospective Studies , Switzerland/epidemiology
20.
Braz. j. microbiol ; 43(4): 1319-1326, Oct.-Dec. 2012. ilus, tab
Article in English | LILACS | ID: lil-665815

ABSTRACT

The availability of a useful tool for simple and timely detection of the most important virulent varieties of Escherichia coli is indispensable. To this end, bacterial DNA pools which had previously been categorized were obtained from isolated colonies as well as selected in terms of utilized phenotype; the pools were assessed by two PCR Multiplex for the detection of virulent E. coli eaeA, bfpA, stx1, stx2, ipaH, ST, LT, and aatA genes, with the 16S gene used as DNA control. The system was validated with 66 fecal samples and 44 wastewater samples. At least one positive isolate was detected by a virulent gene among the 20 that were screened. The analysis of fecal samples from children younger than 6 years of age detected frequencies of 25% LT positive strains, 8.3% eae, 8.3% bfpA, 16.7% ipaH, as well as 12.5 % aatA and ST. On the other hand, wastewater samples revealed frequencies of 25.7% eaeA positive, 30.3% stx1, 15.1% LT and 19.7% aatA. This study is an initial step toward carrying out epidemiological field research that will reveal the presence of these bacterial varieties.


Subject(s)
Child , Wastewater/analysis , Bacteriological Techniques , Disease Outbreaks , Escherichia coli Infections , Escherichia coli/genetics , Escherichia coli/isolation & purification , Genes, Bacterial , Phenotype , Diarrhea, Infantile , Methods , Patients , Virulence
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