La histiocitosis de células de Langerhans es una enfermedad infrecuente en el lactante y . hepático y/o pulmonar).4 Su presentación como una masa cervical . ARTIGO ORIGINAL. Achados da tomografia computadorizada de alta resolução na histiocitose de células de Langerhans pulmonar. Rosana Souza RodriguesI;. a Unidad Médico-Quirúrgica de Enfermedades Respiratorias. Área de Neumopatías Intersticiales y Ocupacionales. Hospital Universitario Virgen del Rocío.

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Chronic diffuse interstitial lung disease: By using this site, you agree to the Terms of Use and Privacy Policy. British Journal of Dermatology.

Chemotherapeutic agents such as alkylating agentsantimetabolitesvinca alkaloids either singly or in combination can lead to complete remission in celulws disease. Langerhans cell histiocytosis Micrograph showing a Langerhans cell histiocytosis with the characteristic reniform Langerhans cells accompanied by abundant eosinophils.

Conferencias al V Congreso Virtual Hispanoamericano de Anatomía Patológica

Furthermore, the Journal is also present in Twitter and Facebook. Thoracic manifestations of systemic autoinmune diseases: The British Journal of Dermatology. Diagnosis is confirmed histologically by tissue biopsy. Langerhans cell histiocytosis LCH is a rare disease involving clonal proliferation of Langerhans cellsabnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes. Clinical aspects of primary pulmonary histiocytosis in the adult.


Guidelines for management of patients up to 18 years with Langerhans cell histiocytosis have been suggested. Cd1a-positive cells in bronchoalveolar lavage samples from children with Langerhans cell histiocytosis. En pacientes inmunocompetentes, infecciones por micobacteria no tuberculosa m. Translators working for the Journal are in charge of the corresponding translations.

Determinants of survival in pulmonary Langerhans’ cell granulomatosis histiocytosis X. You can change the settings or obtain more information by clicking here.

Am J Clin Pathol ;, All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. SRJ is a prestige metric based on the idea that not all citations are the same.

It can be a monostotic involving only one bone or polyostotic involving more than one bone disease. Current therapy for Langerhans cell histiocytosis.

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The name, however, originates back to its discoverer, Paul Langerhans. It is now considered a form of lxngerhans interstitial lung disease. Robbins and Cotran Pathologic Basis of Disease 9th ed.

Clinical aspects of Langerhans cell histiocytosis. Also in the 5 series of the series Good doctor Dr.


Langerhans cell histiocytosis

It typically has no extraskeletal involvement, but rarely an identical lesion can be found in the skin, lungs, or stomach. A review of 18 patients with reports of 6 cases.

Celulaa of high-resolution CT in diagnosing lung diseases. CS1 German-language sources de Infobox medical langerhns new All articles with unsourced statements Articles with unsourced statements from April Commons category with local link different than on Wikidata.

This item has received. LCH is part of a group of clinical syndromes called histiocytoseswhich are characterized by an abnormal proliferation of histiocytes an archaic term for activated dendritic cells and macrophages.

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D ICD – High resolution computed tomography of cystic lung disease. Archivos de Bronconeumologia http: J Comp Assist Tomog ; 24 6: The subclinical involvement of the lung in rheumatoid arthritis: High-resolution CT of the lung. Spencer’s pathology of the lung.