32 research outputs found

    Granular cell tumors of the urinary bladder

    Get PDF
    BACKGROUND: Granular cell tumors (GCTs) are extremely rare lesions of the urinary bladder with only nine cases being reported in world literature of which one was malignant. Generally believed to be of neural origin based on histochemical, immunohistochemical, and ultrastructural studies; they mostly follow a clinically benign course but are commonly mistaken for malignant tumors since they are solid looking, ulcerated tumors with ill-defined margins. MATERIALS AND METHODS: We herein report two cases of GCTs, one benign and one malignant, presenting with gross hematuria in a 14- and a 47-year-old female, respectively. RESULTS: Histopathology revealed characteristic GCTs with positive immunostaining for neural marker (S-100) and negative immunostaining for epithelial (cytokeratin, Cam 5.2, AE/A13), neuroendocrine (neuron specific enolase, chromogranin A, and synaptophysin) and sarcoma (desmin, vimentin) markers. The benign tumor was successfully managed conservatively with transurethral resection alone while for the malignant tumor, radical cystectomy, hysterectomy with bilateral salpingo-oophorectomy, anterior vaginectomy, plus lymph node dissection was done. Both cases show long-term disease free survival. CONCLUSION: We recommend careful pathologic assessment for establishing the appropriate diagnosis and either a conservative or aggressive surgical treatment for benign or localized malignant GCT of the urinary bladder, respectively

    Regional differences in psychiatric disorders in Chile

    Get PDF
    BACKGROUND: Psychiatric epidemiological surveys in developing countries are rare and are frequently conducted in regions that are not necessarily representative of the entire country. In addition, in large countries with dispersed populations national rates may have low value for estimating the need for mental health services and programs. METHODS: The Chile Psychiatric Prevalence Study using the Composite International Diagnostic Interview was conducted in four distinct regions of the country on a stratified random sample of 2,978 people. Lifetime and 12-month prevalence and service utilization rates were estimated. RESULTS: Significant differences in the rates of major depressive disorder, substance abuse disorders, non-affective psychosis, and service utilization were found across the regions. The differential prevalence rates could not be accounted by socio-demographic differences between sites. CONCLUSIONS: Regional differences across countries may exist that have both implications for prevalence rates and service utilization. Planning mental health services for population centers that span wide geographical areas based on studies conducted in a single region may be misleading, and may result in areas with high need being underserved

    The immature stages of Neoscelis dohrni (Westwood) (Coleoptera: Scarabaeidae: Cetoniinae: Goliathini) with notes on adult behavior

    No full text
    Detailed description of the second instar larva and pupa, comparative comments on the third instar and first instar larvae, and some observations on the adult behavior and the life cycle of Neoscelis dohrni (Westwood) are presented. Diagnostic structures are illustrated, and a key to the known third instar larvae of Goliathini from the world is included

    Utilización de la reacción en cadena de la polimerasa para amplificar dos secuencias del gen glicina decarboxilasa que codifica para la proteína P del sistema de clivaje de la glicina, relacionado con hiperglicinemia no cetósica

    Get PDF
    Los Errores Congénitos del Metabolismo son trastornos bioquímicos de origen genético, que causan un defecto específico en la estructura o función de las moléculas proteicas involucradas en una vía metabólica.Dentro de los errores innatos del metabolismo se encuentra la hiperglicinemia no cetósica (HNC), la cual es un desorden autosómico recesivo, que se caracteriza por un defecto en el sistema de clivaje de la glicina, (SCG) ocasionando la acumulación de este aminoácido en los diferentes fluidos corporales, causando alteraciones neurológicas y desórdenes somáticos que llegan a ser letales. El SCG es un sistema multienzimático de carácter mitocondrial y está compuesto por cuatro proteínas individuales reconocidas como proteína P (piridoxal fosfato), H (ácido lipóico), T (tetrahidrofolato) y L (deshidrogenasa lipoamida) (1). La proteína P es codificada por el gen glicina decarboxilasa (GLDC) (2); se han reportado varias mutaciones en este gen, siendo la mutación S564I, la más común (3). La actividad de esta proteína se encuentra disminuida o ausente en 80% de los pacientes con HNC (4). Los estudios de esta entidad en Colombia, se iniciaron con Barrera y col (5), pero no se disponía de un diagnóstico enzimático ni molecular para la HNC; por lo tanto, la Universidad Colegio Mayor de Cundinamarca, en asociación con la unidad de biología procreativa del Instituto Materno Infantil y la Universidad Nacional de Colombia, inició el estudio bioquímico y molecular de esta enfermedad
    corecore