Solitary Langerhans cell histiocytosis of the hard palate: a diagnostic pitfall
Langerhans cell histiocytosis (LCH) is a relatively rare and unique disease characterized by an abnormal proliferation of immature dendritic cells. It is predominantly seen in children with adults showing less than ten times the incidence compared to ...
Varsha, Dalal +7 more
core +1 more source
Endocrine manifestations in Langerhans cell histiocytosis.
Langerhans cell histiocytosis is a rare, multisystem disease that shows a particular predilection for hypothalamo-pituitary axis involvement. Diabetes insipidus is the most frequent permanent consequence of Langerhans cell histiocytosis, developing in ...
Chrousos, GP +4 more
core +1 more source
Langerhans cell histiocytosis (LCH) is a rare disease involving multiple systems, and it is caused by excessive proliferation of Langerhans cells. The hypothalamic-pituitary region (HPR) is involved in 5%-50% of all LCH patients, particularly those with ...
Murat Şahin +3 more
core +1 more source
Generalized indeterminate cell histiocytosis successfully treated with methotrexate
Erina Lie, MD +3 more
doaj +1 more source
A death from Langerhans cell histiocytosis and tuberculosis in 18th Century Hungary - what palaeopathology can tell us today [PDF]
Spigelman, M, Pap, I, Donoghue, HD
core
Histiocyte Society blueprint for non-Langerhans cell histiocytosis research: unraveling complex diseases through collaboration. [PDF]
Hershkovitz-Rokah O +3 more
europepmc +1 more source
Molecular Profiling of Tumor Tissue and Plasma Cell-Free DNA from Patients with Non-Langerhans Cell Histiocytosis. [PDF]
Janku F +9 more
europepmc +1 more source
Case report: Pulmonary non-Langerhans cell histiocytosis in a dog with acute interstitial granulomatous pneumonia. [PDF]
Granger KL +4 more
europepmc +1 more source
Treatment of Langerhans Cell Histiocytosis
Histiocytosis X patients present with a variety of clinical manifestations and outcomes. The principal difficulty in the establishment of a definite protocol for treatment is based on the poor understanding of the basic nature of this disease, the ...
김현우, 신규호
core
Extensive reactive cutaneous histiocytic infiltrate resembling non-Langerhans cell histiocytosis as the presenting sign of underlying vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome. [PDF]
Wang CX +3 more
europepmc +1 more source

