Results 131 to 140 of about 9,769 (177)

Bilateral temporal skull xanthoma characterized as a Langerhans cell histiocytosis: a case report. [PDF]

J Med Case Rep
Liu H, Tian H, Xu S.
europepmc   +1 more source

Vertebral involvement in Erdheim-Chester disease: a case report of non-BRAF-driven diagnosis and treatment challenges. [PDF]

Front Oncol
Zhao H, Xie W, Lin S, Wu L, Wu W.
europepmc   +1 more source

Erdheim-Chester Disease Presenting as a Suprasellar Mass. [PDF]

Cureus
Bandhlish A, White-Dzuro GA, Barkley A, Hanak B, Latimer CS, Cecchini MM, Gonzalez-Cuyar L, Ferreira M.   +7 more
europepmc   +1 more source

Hepatic Involvement as the Initial Manifestation of Adult Langerhans Cell Histiocytosis. [PDF]

ACG Case Rep J
Rajeev M, Narayan A, Agrawal N, Jaleel J, Arora V, Sarin SK.   +5 more
europepmc   +1 more source

Rosai-Dorfman disease mimicking molluscum contagiosum in a patient with prior kappa light chain multiple myeloma. [PDF]

JAAD Case Rep
Rivas S, Li N, Alicea DS, Andriano TM, Zengin H, Amin B, McLellan BN.   +6 more
europepmc   +1 more source

Prognostic factor analysis of oral and maxillofacial Langerhans cell histiocytosis based on clinical findings and tumour microenvironment. [PDF]

BMC Oral Health
Ogawa M, Yokoo S, Saitou E, Seki M, Yamaguchi T, Suzuki K, Nakamura H, Makiguchi T.   +7 more
europepmc   +1 more source

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Biology of Langerhans Cells and Langerhans Cell Histiocytosis

International Review of Cytology, 2006
Langerhans cells (LC) are epidermal dendritic cells (DC). They play an important role in the initiation of immune responses through antigen uptake, processing, and presentation to T cells. Langerhans cell histiocytosis (LCH) is a rare disease in which accumulation of cells with LC characteristics (LCH cells) occur. LCH lesions are further characterized
R J Arceci, R M Egeler
exaly   +3 more sources

Adult Langerhans cell histiocytosis

European Journal of Haematology, 2006
Abstract:  Langerhans cell histiocytosis (LCH) is a proliferative histiocytic disorder of unknown cause originating from dendritic cells. The clinical presentation of LCH is highly variable. Although the features of this disease have been well described in children, they remain poorly defined in adults. Here, we review the current knowledge about adult
Marcus, Stockschlaeder, Christoph, Sucker   +1 more
exaly   +3 more sources

Langerhans cell histiocytosis

Journal of the American Academy of Dermatology, 2001
From the Department of Radiology, Division of Neuroradiology,a and the Department of Dermatology,b Indiana University Medical Center; and the Department of Oral Surgery Medicine and Pathology, Indiana University School of Dentistry.c Reprint requests: Ginat W. Mirowski, DMD, MD, Department of Dermatology, 550 N University Blvd, Suite 3240, Indianapolis,
K S, Caldemeyer, E T, Parks, G W, Mirowski   +2 more
  +7 more sources