Results 11 to 20 of about 12,716 (134)
High prevalence of myeloid neoplasms in adults with non–Langerhans cell histiocytosis [PDF]
Key Points Some 10.1% of adults with non–Langerhans cell histiocytosis have a concomitant myeloid neoplasm with each often harboring distinct mutations. The presence of distinct kinase mutations in histiocytosis and myeloid neoplasms resulted in discordant responses to targeted therapy.
Papo, Matthias+22 more
semanticscholar +6 more sources
Abstract Erdheim-Chester disease (ECD) and Rosai-Dorfman disease (RDD) are rare non-Langerhans cell histiocytoses (non-LCHs), for which therapeutic options are limited. MAPK pathway activation through BRAFV600E mutation or other genomic alterations is a histiocytosis hallmark and correlates with a favorable response to BRAF inhibitors ...
Ashley Aaroe+12 more
semanticscholar +4 more sources
Molecular Profiling of Tumor Tissue and Plasma Cell-Free DNA from Patients with Non-Langerhans Cell Histiocytosis [PDF]
Abstract The BRAFV600E mutation and BRAF inhibitor responsiveness characterize ∼50% of patients with the non-Langerhans cell histiocytosis (non-LCH) Erdheim–Chester disease (ECD). We interrogated the non-LCH molecular landscape [ECD, n = 35; Rosai–Dorfman disease (RDD), n = 3; mixed ECD/RDD, n = 1] using BRAFV600E PCR and/or next ...
Janku, Filip+9 more
semanticscholar +6 more sources
AbstractErdheim-Chester disease is a rare non-Langerhans histiocytosis with multisystem involvement. To date, there is no standard treatment for this disorder, and more than half of the patients succumb within 3 years. Because interferon-α promotes the terminal differentiation of histiocytes and dendritic cells, we hypothesized that this molecule would
Bita Esmaeli+7 more
semanticscholar +5 more sources
Disseminated non-Langerhans cell histiocytosis with an IRF2BP2-NTRK1 gene fusion identified by next-generation sequencing [PDF]
Beth A. Martin+7 more
semanticscholar +6 more sources
restriction
Jemin Kim, Yeongjoo Oh, Chang Ook Park
openaire +5 more sources
BackgroundPulmonary involvement of Non-Langerhans Cell Histiocytosis (PNLCH) is a rare cause of interstitial pulmonary disease in people and are classified as either Erdheim-Chester disease (ECD) or Rosai-Dorfman disease (RDD). In veterinary medicine, feline pulmonary Langerhans cell histiocytosis (PLCH) has been identified as an infiltrative ...
Kyle L. Granger+4 more
openaire +4 more sources
A RARE CASE OF PULMONARY NON-LANGERHANS CELL HISTIOCYTOSIS [PDF]
Kristen Hughes+3 more
openaire +3 more sources
Langerhans Cell Histiocytosis (LCH) and the non-LCH, Erdheim Chester Disease, are rare histiocytic neoplasms with distinctive clinical and immunophenotypic features, but with several overlapping molecular features. LCH is a neoplasm of Langerin-positive, CD1a-positive, S100-positive dendritic cells (DCs), once thought to arise from the epidermal or ...
Liqiang Xi+3 more
openaire +4 more sources
NON-LANGERHANS CELLS HISTIOCYTOSIS ASSOCIATED WITH SYSTEMIC LUPUS ERYTHEMATOSUS - CASE REPORT
Edgard Torres dos Reis Neto+10 more
openaire +2 more sources