Langerhans cell histiocytosis: a rare cause of cholestasis in adult patients. Case report. Histiocitosis de Langerhans: causa infrecuente de colestasis en el. a Unidad Médico-Quirúrgica de Enfermedades Respiratorias. Área de Neumopatías Intersticiales y Ocupacionales. Hospital Universitario Virgen del Rocío. Abstract. GOMEZ, ANA MARÍA et al. Langerhans cell histiocytosis in children. A description of 10 cases. CES Med. [online]. , vol, n.2, pp
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Histiocytosis; Langerhans cells; Pediatrics.
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 hixtiocitosis. Case report Histiocitosis de Langerhans: Print Send to a friend Export reference Mendeley Statistics. A biopsy of the lesions showed that these lesions were compatible with Langerhans cell histiocytosis.
d April Pages Subscribe to our Newsletter. Translators working for the Journal are in charge of the corresponding translations. Pulmonary Langerhans cell histiocytosis: To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Ann Thoracic Surg, 30pp.
It gives few symptoms, and it is usually diagnosed in the autopsy 3where fibrosis may prevail over histiocytosic infiltration. How to cite histioctosis article. CiteScore measures average citations received per document published.
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SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. A liver biopsy was performed after ruling out common pathologies. Manuscripts will be submitted electronically using the following web site: 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 diagnosis is based on pathological study of a biopsy of the organ involved.
The disease prognosis and its response to treatment is better lanterhans the single system form, particularly with bone involvement, and much worse in the multi-system form, especially if several risk organs are involved liver, spleen, bone marrow and lung. Previous article Next article.
Etxezarraga 2 and M.
Histiocitosis de células de Langerhans en niños. Descripción de 10 casos
The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: The patient’s liver function gradually worsened and he was taken to a centre of reference for a liver transplant, he died before it could be performed.
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Full text is only aviable in PDF. Liver involvement in Langerhans’ cell histiocytosis: Other types of articles such as reviews, editorials, special articles, clinical reports, and letters to the Editor are also published in the Dde.
It is a monthly Journal that publishes a total of 12 issues, which contain these types of articles to different extents.
Continuing navigation will be considered as acceptance of this use. The main pathological finding is the presence of an accumulation of Langerhans histiocytes, which ce distinctive nuclei features a central “coffee bean” shaped folding, fine chromatin, and oval shaped nuclei that distinguishes them from conventional histiocytes.
However, if risk organs are involved, other chemotherapeutics are needed as well 6-mercaptopurine and metotrexate. We present a 42 year old man, with a history of central dde insipidus since childhood, primary hyperthyroidism with negative antibodies and seizures since early adulthood. Liver involvement in Langehan’s cell histiocytosis. Continuing navigation will be considered as acceptance of this use.
Pancreatic involvement is very rare.