Results 121 to 130 of about 14,204,415 (185)

Solitary Langerhans cell histiocytosis of the hard palate: a diagnostic pitfall

open access: yes, 2016
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.

open access: yes, 2007
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

A Case of Langerhans Cell Histiocytosis Presenting with Suprasellar Mass and Panhypopituitarism Clinic

open access: yes
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

open access: yesJAAD Case Reports, 2022
Erina Lie, MD   +3 more
doaj   +1 more source

Molecular Profiling of Tumor Tissue and Plasma Cell-Free DNA from Patients with Non-Langerhans Cell Histiocytosis. [PDF]

open access: yesMol Cancer Ther, 2019
Janku F   +9 more
europepmc   +1 more source

Treatment of Langerhans Cell Histiocytosis

open access: yes, 1996
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  

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