a Unidad Médico-Quirúrgica de Enfermedades Respiratorias. Área de Neumopatías Intersticiales y Ocupacionales. Hospital Universitario Virgen del Rocío. OSSES A, RODRIGO; GONZALEZ B, SERGIO; AGUIRRE Z, MARCIA SALDIAS P, FERNANDO. Histiocitosis de células de Langerhans pulmonar: Caso clínico. La histiocitosis de células de Langerhans es una enfermedad . Tras plantearse el caso como histiocitosis hepático y/o pulmonar).4 Su presentación.
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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.
Langerhans cell histiocytosis – Wikipedia
Other types of articles such as reviews, editorials, special articles, clinical reports, and letters to the Editor are also published in the Journal. The pathogenesis of Langerhans cell histiocytosis LCH is a matter of debate. After six months of follow up, histiocitpsis patient is in good conditions. On the other hand, the infiltration of organs by monoclonal population of pathologic cells, and the successful hitsiocitosis of subset of disseminated disease using chemotherapeutic regimens are all consistent with a neoplastic process.
Retrieved from ” https: Gary 21 July Wikimedia Commons has media related to Langerhans Cell Histiocytosis. Open biopsy for chronic diffuse infiltration lung disease: It is now considered a form of smoking-related interstitial lung disease. Manuscripts will be submitted electronically using the following web site: LCH is usually a sporadic and non- hereditary condition but familial clustering has been noted in limited number of cases.
Langerhans cell histiocytosis is occasionally misspelled as “Langerhan” or “Langerhan’s” cell histiocytosis, even in authoritative textbooks. N Engl J Med,pp. The latter may be evident in chest X-rays with micronodular and interstitial infiltrate in the mid and lower zone of lung, with sparing of the Costophrenic angle or honeycomb appearance in older lesions.
The American Journal of Surgical Pathology. It is a monthly Journal that publishes a total of 12 issues, histoicitosis contain these types of articles to different extents.
Histiocitosis de células de Langerhans pulmonar: Caso clínico
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Excellent for single-focus disease. Robbins and Cotran Pathologic Basis of Disease 9th ed.
These diseases are related to other forms of abnormal proliferation of white blood cellssuch as leukemias and lymphomas. Eur Respir J, 9pp. Determinants of survival in pulmonary Langerhans’ cell granulomatosis histiocytosis X.
It is mostly seen in children under age 2, and the prognosis is poor: However systemic diseases often require chemotherapy. Print Send to a friend Export reference Mendeley Statistics. Two pulmobar studies have confirmed this finding. All manuscripts are sent to peer-review and handled by the Editor or an Associate Editor from the team.
Langerhans cell histiocytosis
In other projects Wikimedia Commons. Chest,pp. The name, however, originates back to its discoverer, Paul Langerhans.
MRI and CT puomonar show infiltration in sella turcica. Guidelines for management of patients up to 18 years with Langerhans cell histiocytosis have been suggested.
Writing Group of the Histiocyte Society”. These cells in combination with lymphocyteseosinophilsand normal histiocytes form typical LCH lesions that can be found in almost any organ.