Results 121 to 130 of about 9,387 (173)

Cutaneous Limited Langerhans Cell Histiocytosis Complicated by Late-onset Panhypopituitarism. [PDF]

JCEM Case Rep
Ahmed N, Davidge-Pitts C, Johnson E, Young J, Go RS.   +4 more
europepmc   +1 more source

Survival outcomes and adverse prognostic factors of Langerhans cell histiocytosis: a 40-year experience from a single tertiary center in Thailand. [PDF]

Ann Hematol
Atirattanachai G, Songthawee N, Sripornsawan P, Yam-Ubon U, Chotsampancharoen T.   +4 more
europepmc   +1 more source

Pulmonary Langerhans cell histiocytosis: A case series and literature review. [PDF]

J Clin Imaging Sci
Carbone RG, Roden AC, Huntley CC, Puppo F.   +3 more
europepmc   +1 more source

Bile Duct Targeting or Preservation: Contrasting Liver Histology in Langerhans Cell Histiocytosis and Disseminated Juvenile Xanthogranuloma. [PDF]

Pediatr Dev Pathol
Däniker M, Baleydier F, Rock NM, Menzinger S, Wildhaber BE, McLin VA, Rougemont AL.   +6 more
europepmc   +1 more source

Stereotactic radiosurgery for intracranial Langerhans cell histiocytosis: A multi-institutional case series with long-term follow-up. [PDF]

Brain Spine
Duzkalir AH, Yildirim DC, Almeida T, Niranjan A, Lunsford LD, Moreno NM, Álvarez RM, Peker S.   +7 more
europepmc   +1 more source

Langerhans Cell Histiocytosis

Survey of Ophthalmology, 2008
The clinical manifestations of Langerhans cell histiocytosis have been recognized for more than a century. For most of that time, physicians have viewed the disease from different perspectives, interpreting portions of its clinical spectrum as if they were distinct and unrelated entities.
Curtis Edward Margo
exaly   +6 more sources

Langerhans-Cell Histiocytosis [PDF]

New England Journal of Medicine, 2018
Langerhans-Cell Histiocytosis A spectrum of diseases formerly known as histiocytosis X and now called Langerhans-cell histiocytosis is characterized by ERK pathway activation (including BRAF V600E ...
Miriam Merad, Kenneth L Mcclain
exaly   +5 more sources

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Langerhans cell histiocytosis

Skeletal Radiology, 2006
Langerhans cell histiocytosis (LCH) is a complex disease entity comprised of three distinct clinical syndromes that demonstrate indistinguishable histology. These syndromes are: eosinophilic granuloma, which is predominantly osseous or pulmonary; Hand-Schûller-Christian's disease, which involves multiple organ systems and, most typically, the skull ...
Kevin Bradford, Hoover, Daniel I, Rosenthal, Henry, Mankin   +2 more
openaire   +4 more sources

Langerhans Cell Histiocytosis

Journal of Cutaneous Medicine and Surgery, 2012
Background: The cutaneous presentation of Langerhans cell histiocytosis (LCH) is very rare and can be highly variable among individuals, which can often lead to a delay in diagnosis. Objective: To discuss a case report and literature review of important clinical indicators, histology, diagnosis, evaluation, and treatment guidelines.
Ligaya, Park, Clayton, Schiltz, Neil, Korman   +2 more
openaire   +2 more sources