HISTIOCITOSIS DE CELULAS DE LANGERHANS PEDIATRIA PDF

Discussion: la histiocitosis de células de Langerhans es una enfermedad de compromiso sistémico muy poco frecuente en pediatría, de diversas formas de. (1)Servicio de Clínica Médica, Hospital de Pediatría Juan P. Garrahan, Ciudad Publisher: La histiocitosis de células de Langerhans es una. Histiocitosis congénita de células de Langerhans multisistémica. Revista de la Sociedad Boliviana de Pediatría. Open Journal Systems · Journal Help. User.

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Histiocitosis de células de Langerhans en niños. Descripción de 10 casos

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Continuing navigation will be considered as acceptance of this use. A description of 10 cases. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate.

Gastrointestinal involvement in Celulws cell histiocytosis. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

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CiteScore measures average citations received per document published. Langerhans cell histiocytosis in children.

Services on Demand Article. Retrospective study in pediatric patients diagnosed in the Valle del Lili Foundation over a period of six years.

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas of pediatrics. Histiocytosis; Langerhans cells; Pediatrics. Histiocktosis continua navegando, consideramos que acepta su uso.

Of the 10 patients 5 had risk organ involvement and 1 died in the observation period. Cl 10 A- The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: The goal with the description of this cases series is to highlight the importance and awareness to a timely diagnosis and management of this entity, for a better quality of life and longer survival. Langerhans cell histiocytosis is a rare disease with different clinical and pathological presentation, is laangerhans divided into three groups: How to cite this article.

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In our series of cases there was no gender difference and the mean age at presentation was 33 months. Are you a health professional able to histiocjtosis or dispense drugs?

SRJ is a prestige metric based on the idea that not all citations are the same. In the diagnosis by immunohistochemistry identified Langerhans Cell Histiocytosis, the cases were classified as multisystemic -multifocal in 5 patients, unisystemic in 1 patients – unifocal unisystemic in 1 patients -multifocal eosinophilic granuloma in 3 patients.