Management of adult patients with Langerhans cell histiocytosis: recommendations from an expert panel on behalf of Euro-Histio-Net [PDF]
core +1 more source
Extra-osseous involvement of Langerhans' cell histiocytosis in children [PDF]
The predominant clinical and radiological features of Langerhans' cell histiocytosis (LCH) in children are due to osseous involvement. Extra-osseous disease is far less common, occurring in association with bone disease or in isolation; nearly all ...
Eich, Georg +5 more
core
Current diagnostic status of bronchoalveolar lavage studies [PDF]
Broncboalveolar lavage using flexible fiberoptic bronchoscopy has emerged as a powerful investigative tool in respiratory medicine. It has helped in better understanding of pathogenesis of various interstitial lung diseases especially idiopathic ...
Vijayan, V K
core
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 +3 more sources
Langerhans Cell Histiocytosis Presenting with Headache and Sellar Mass in an Adult [PDF]
Bhattacharya, Rajib K +3 more
core +2 more sources
Generalized indeterminate cell histiocytosis successfully treated with methotrexate
Erina Lie, MD +3 more
doaj +1 more source
Mucosa associated lymphoid tissue lymphoma of the thyroid gland: a case report and literature review = MALT linfoma della tiroide: caso clinico e revisione della letteratura [PDF]
Mucosa associated lymphoid tissue (MALT) lymphomas are low-grade, non-Hodgkin’s B cell lymphomas, mainly occurring in the gastrointestinal tract, but also in other tissues.
Attene, Federico +5 more
core
Non-langerhans cell histiocytosis involving the spleen - Erdheim-Chester disease: a case report
Erdheim-Chester Disease (ECD) is a rare form of non-Langerhans histiocytosis characterized by the proliferation of CD68+, CD1a-, and CD163+ histiocytes, with potential multisystem involvement. We report the case of a 31-year-old male presenting with refractory abdominal pain and splenomegaly.
Giovanna Lage Fagunde +3 more
openaire +1 more source
Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report [PDF]
Khalid A Al-Anazi +20 more
core +1 more source
NON-LANGERHANS CELLS HISTIOCYTOSIS ASSOCIATED WITH SYSTEMIC LUPUS ERYTHEMATOSUS - CASE REPORT
Izaura Tereza Silva Guedes +10 more
openaire +1 more source

