Langerhans Cell Histiocytosis: Emerging Insights and Clinical Implications. [PDF]
Langerhans cell histiocytosis is a disorder characterized by lesions that include CD207+ dendritic cells along with an inflammatory infiltrate. Langerhans cell histiocytosis has a highly variable clinical presentation, ranging from a single lesion to ...
Allen, Carl E +2 more
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Langerhans Cell Histiocytosis [PDF]
Sandra, Camelo-Piragua +2 more
openaire +2 more sources
MR of the hypothalamic-pituitary axis in Langerhans cell histiocytosis. [PDF]
To describe the MR findings in the hypothalamic pituitary area in children with Langerhans cell histiocytosis and to define those MR alterations especially associated with the risk of developing diabetes insipidus.The hypothalamic-neurohypophyseal axis ...
GENOVESE, EUGENIO ANNIBALE +5 more
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A case of diagnosis and treatment of mediastinal Langerhans cytosis
Background Langerhans cell histiocytosis (LCH) is a rare disease. It mainly involves abnormal proliferation and aggregation of Langerhans cells, a type of cell of the immune system.Langerhans cytosis is more common in the bone, but it has rarely been ...
Yumeng Niu +5 more
doaj +1 more source
Unifocal langerhans cell histiocytosis presenting as an aggressive bone lesion [PDF]
Objective To discuss a case of unifocal Langerhans cell histiocytosis (eosinophilic granuloma) presenting as an aggressive osseous destructive process.
George, S., Young, K.J.
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Unusual Neurological Manifestation of Langerhans Cell Histiocytosis in an Adult
Langerhans Cell Histiocytosis is a rare disorder characterized by an abnormal proliferation of Langerhans cells in one or multiple organs. It rarely presents with a central vestibular involvement.
Imen Achour MD +7 more
doaj +1 more source
Langerhans cell histiocytosis: literature review and descriptive analysis of oral manifestations [PDF]
Langerhans cell histiocytosis (LCH) is a rare disease, of unknown pathogenesis, characterized by intense and abnormal proliferation of bone marrow-derived histiocytes (Langerhans cells).
Guerrero-Rodríguez, V +3 more
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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
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Cutaneous Rosai-Dorfman-Destombes disease: the diagnostic value of the yellow island sign. [PDF]
El Maati M +4 more
europepmc +1 more source
A Rare Soft Tissue Presentation of Mixed Histiocytosis with Multiple Disseminated Subcutaneous Masses. [PDF]
Miyagawa F +4 more
europepmc +1 more source

