Istiocitosi x pdf

2019-08-21 10:10

Feb 01, 1982 Request PDF on ResearchGate On Feb 1, 1982, F Mangini and others published [Histiocytosis X. For full functionality of ResearchGate it is necessary to enable JavaScript.Oct 25, 2012 Langerhans cell histiocytosis (LCH) is a heterogeneous disease, characterized by accumulation of dendritic cells with features similar to epidermal Langerhans cells in various organs. Any organ or system of the human body can be affected, but those more frequently involved are the skeleton (80 of cases), the skin (33), and the pituitary (25). istiocitosi x pdf

Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes. Clinically, its manifestations range from isolated bone lesions to multisystem disease.

Istiocitosi X By STELLA G, BAGLIANI GP, CAMPANACCI M, CAPANNA R, CIGALA F, FORMICA C, GANDUS S, IPPOLITO E, MASTRAGOSTINO S, MERCURI M, RAVAGLIA M, SCARSI M and VALLE GM Abstract Gli autori riferiscono su un caso di diabete insipido insorto acutamente, riscontrato in una paziente affetta da Istiocitosi X. Sono discussi i reperti RM, consistenti in un marcato ispessimento del peduncolo ipofisario e scomparsa dell'iperintesit di segnale della neuroipofisi nelle immagini sagittali T1pesate. istiocitosi x pdf Langerhans cell histiocytosis (LCH) is a rare multisystem disease with a wide and heterogeneous clinical spectrum and variable extent of involvement. Terminology Langerhans cell histiocytosis was previously known as histiocytosis X. The newer

Download PDF: Sorry, we are unable to provide the full text but you may find it at the following location(s): (external link) istiocitosi x pdf Langerhans cell histiocytosis in children: from the bench to bedside for an updated therapy Maurizio Arico Azienda Sanitaria Regionale, Ragusa, Italy CLINICAL IMAGES Annals of African Medicine Volume 8, No. 1, March 2009 Histiocytosis X (Langerhans cell granulomatosis) is a disease of unknown aetiology, but viral origin has histiocytosis1 1. Langerhan's cell disease 2. Xanthogranuloma family 3. Indeterminate cell histiocytosis A case of a 11 years old female who had presented a diabetes insipidus 7 years before caused by a CTdemostrated expansive mass located in the hypothalamic region, treated by radiation therapy.

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