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Showing 1 to 6 of 6 for “"Histiocytosis"”.
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Σύγχρονα δεδομένα για τη διάγνωση και θεραπεία της ιστιοκύττωσης Langerhans / Current concepts for the diagnosis and management of Langerhans cell histiocytosis
Η ιστιοκύττωση Langerhans αποτελεί σπάνια ιστιοκυτταρική διαταραχή με ιδιαίτερα ετερογενή κλινική εικόνα, η οποία μπορεί να κυμαίνεται από εντοπισμένη, αυτοϊώμενη νόσο έως πολυσυστηματική μορφή με σοβαρή νοσηρότητα και αυξημένη θνητότητα. Η νόσος χαρακτηρίζεται από κλωνικό πολλαπλασιασμό …
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Outcomes of children with biopsy-proven Langerhans cell histiocytosis (LCH) treated at the Red Cross War Memorial Children's Hospital from 1998 – 2017
Background: Langerhans Cell Histiocytosis (LCH) is a rare histiocytic disorder characterised by the infiltration of a single organ or multiple organs by cells phenotypically similar to Langerhans cells. The number and type of systems involved affect the outcome and the longer the maintenance …
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The Non-Medical Expenses Associated with Childhood Cancer
… (n=4), brain tumors (n=3), lymphomas (n=3), and histiocytosis (n=l).<br> Categories of expenses included food, travel, lodging, clothing, child care, and miscellaneous items. Weekly expenditures ranged from 0-$698 (x $233.15). The total amount of lost income since the time of diagnosis ranged …
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Το ηωσινόφιλο κοκκίωμα των οστών: από ορθοπεδική άποψη
… OCCURED, NO TRANSITION TO OTHER SYNDROMS OF HISTIOCYTOSIS X, WAS OBSERVED NEITHER CLINICALLY NOR HISTOLOGICALLY AFTER BIOPSY IN NEW LOCALIZATIONS. FINALLY ALL RECHECKED PATIENTS ARE SYMPTOMS FREE EXCEPT ONE WITH RECENT RELAPSE.
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Investigating lesions of Langerhans cells and their role in Lymphoproliferative diseases
… proliferation of LCs is termed Langerhan’s cell histiocytosis (LCH), an enigmatic and poorly understood disorder with a widely varied clinical spectrum and disease course. In non-pulmonary LCH all cases reported to date have been monoclonal. Clonality argues for LCH as a neoplastic rather than …
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Deficiência de arginina-vasopressina (diabetes insipidus central) como primeira manifestação de histiocitose de células de Langerhans: relato de caso
Introduction: Langerhans cell histiocytosis (LCH) is a rare clonal neoplasm of the mononuclear phagocyte system characterized by proliferation of CD1a⁺/Langerin⁺ myeloid dendritic cells and activating mutations in the MAPK/ERK pathway (such as BRAF V600E and MAP2K1). Involvement of the …