I am a Dek

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.

Author: Malazilkree Goltir
Country: Saint Lucia
Language: English (Spanish)
Genre: Software
Published (Last): 4 July 2013
Pages: 183
PDF File Size: 12.35 Mb
ePub File Size: 12.43 Mb
ISBN: 641-7-18260-532-9
Downloads: 83681
Price: Free* [*Free Regsitration Required]
Uploader: Grojar

Medical and Pediatric Oncology. Print Send to a friend Export reference Mendeley Statistics. Chest,pp. Specialty Hematology 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.

SRJ is a prestige metric based on the idea that not all citations are the same. It can be pulmonat monostotic involving only one bone or polyostotic pklmonar more than one bone disease.

Subscribe to our Newsletter. A high resolution chest CT scan showed multiple cystic structures predominating in the upper lobes, with small centrilobular nodules. September Pages D ICD – Journal of the American Academy of Dermatology. MRI and CT may show infiltration in sella turcica. These cells in combination with lymphocyteseosinophilsand normal histiocytes form typical LCH lesions that can pulmonqr found in almost any organ.

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.


Juvenile xanthogranuloma Hemophagocytic lymphohistiocytosis Erdheim-Chester disease Niemann—Pick disease Sea-blue histiocyte Benign cephalic histiocytosis Generalized eruptive histiocytoma Xanthoma disseminatum Progressive nodular histiocytosis Papular xanthoma Hereditary progressive mucinous histiocytosis Reticulohistiocytosis Multicentric reticulohistiocytosisReticulohistiocytoma Indeterminate cell histiocytosis. European Journal of Cancer.

Peak onset is 2—10 years of age. Two independent studies have confirmed this finding. The Impact Factor measures the average number of hisstiocitosis received in a particular year by papers published in the journal during the two receding years. Also in the 5 series of the series Good doctor Dr. Langerhans cell histiocytosis Micrograph showing a Langerhans cell histiocytosis with the characteristic reniform Langerhans cells accompanied by abundant hiatiocitosis.

You can change the settings or obtain more information by clicking here. This page was last edited on 1 Decemberat Previous article Next article. Among children under the age of 10, yearly incidence is thought to be 1 in ,; [35] and in adults even rarer, in about 1 inLCH usually affects children between 1 and 15 years old, with a peak incidence between 5 and 10 years of age.

This item has received.

Histiocitosis de células de Langerhans pulmonar: Caso clínico

Archived from the histiocutosis on CD1 positivity are more specific. Archivos de Bronconeumologia http: Furthermore, the Journal is also present in Twitter and Facebook. Journal of Clinical Pathology. Endocrine deficiency often require lifelong supplement e. Guidelines for diagnosis, clinical work-up, and treatment for patients till pulmoar age of 18 years”. Radiology will show osteolytic bone lesions and damage to the lung. Views Read Edit View history. The Journal is published both in Spanish and English.


The American Journal of Surgical Pathology.

There was a problem providing the content you requested

International Journal of Pediatric Otorhinolaryngology. Histiocytosis Monocyte- and macrophage-related cutaneous conditions Rare diseases. Robbins and Cotran Pathologic Basis of Disease 9th ed.

Nelson Textbook of Pediatrics 19th ed. Guidelines for management of patients up to 18 years with Langerhans cell histiocytosis have been suggested. Organ involvement can also cause more specific symptoms. British Journal of Haematology. The name, however, originates back to its discoverer, Paul Langerhans.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. From Wikipedia, the free encyclopedia. Hematoxylin-eosin stain of biopsy slide will show features of Langerhans Cell e. CS1 German-language sources de Infobox medical condition new Histioitosis articles with unsourced statements Articles with unsourced statements from April Commons category link is locally defined. Wikimedia Commons has media related to Langerhans Cell Histiocytosis.

Full text is only aviable in PDF. Retrieved from ” https: Histiocitosix cells ; Histiocytosis, Langehaus-cell ; Tobacco smoking. Vidal Serrano aE. Adult pulmonary Langerhans cell histiocytosis PLCH is a rare disorder of unknown etiology that occurs predominantly in young smokers, with an incidence peak at years of age.

Continuing navigation will be considered as acceptance of this use.