Results 111 to 120 of about 24,931 (232)

Histiocytosis-X [PDF]

Proceedings of the Royal Society of Medicine, 1962
J S, Pegum, P, Wallis
openaire   +2 more sources

Histiocytosis X of the thyroid gland.

, 1996
Histiocytosis X rarely involves the thyroid gland and occurs as one of the unusual manifestations of systemic diseases. Diagnosis is based on the identification of the Langerhans' cells in an appropriate background.
Staibano S., Tornillo L, D'Antonio A., Orabona P, D'Antonio A, DE ROSA, GAETANO, Boscaino A, Orabona P., De Rosa G., Boscaino A., Tornillo L., STAIBANO, STEFANIA   +11 more
core  

Urticating histiocytosis: A mast cell-rich variant of histiocytosis X

, 1986
Histiocytosis X and mastocytosis are proliferative processes that may have similar cutaneous manifestations. However, a positive Darier's sign (urtication on stroking of the lesion) is thought to reliably distinguish between these two diseases.
Elliott Foucar, Warren W. Piette, David T. Tse, Tse, David T, Piette, Warren W, Alan D. Olmstead, Foucar, Elliott, James Goeken, Goeken, James, Olmstead, Alan D   +9 more
core   +1 more source

Uncommon variants of Non-Langerhans Cell Histiocytosis [PDF]

, 2019
Background: Histiocytosis are rare disorders of the mononuclear phagocyte system, characterized by a derangement in differentiation, proliferation or function of monocytes and dendritic cells.
Chiara Moltrasio, Arturo Bonometti, Emanuela Passoni, Emanuela De Juli, Gianluca Nazzaro, Marco Paulli, Silvia Alberti-Violetti, Filippo Bagnoli, Emilio Berti, Jessica Gliozzo   +9 more
core   +1 more source

Case Report: Neuropsychiatric instability in structurally compromised CNS Erdheim–Chester disease: a diagnostic and management challenge

Frontiers in Psychiatry
BackgroundErdheim–Chester disease (ECD) is a rare non-Langerhans cell histiocytosis involving multiple systems, with central nervous system (CNS) involvement present in a significant subset.
Abdulaziz F. Alfraiji, Mohamed F. Alqahtani, Shahad Aljudi, Fahad D. Alosaimi   +3 more
doaj   +1 more source

Progressive nodular histiocytosis: a rare type of xanthogranuloma

, 2011
Progressive nodular histiocytosis is a rare non-Langerhans histiocytosis. It tends to occur in adult with progressive course that differentiates from other groups of xanthogranuloma. The clinical presentation is characteristic and disfiguring of the face
Fu-Chen Chuang, Erick Chern, Wei-Ming Wu
core   +1 more source

Infectious Histiocytosis with Pancytopenia and Bone Marrow Hemophagocytosis

, 2002
infectious histiocytosis with pancytopenia & bone marrow ...
Lawrence, Christine
core  

Cerebellar Disease Mimicking Cerebrotendinous Xanthomatosis: Langerhans Cell Histiocytosis

, 2017
Item does not contain fulltextBACKGROUND: This report highlights the differential diagnosis of predominant cerebellar white matter abnormalities with dentate nuclei involvement.
Marjo S. van der Knaap, Aad Verrips, Knaap, M.S. van der, Stelten, B.M.L., Bianca M.L. Stelten, Ron A. Wevers, Verrips, A., Wevers, R.A.   +7 more
core   +1 more source

LCH-Histiocytosis from Langerhans Cells in Craniofacial Region

, 2005
The authors retrospectively analyze the occurrence of histiocytosis from Langerhans cells (LCH) in a group of patients from the Children Stomatological Clinic in Prague - Motol from the years 1998-2003.
J. Kozák, M. Hubáček
core  

Benign and malignant cutaneous nasal lesions

Eye & ENT Research
The nose is a structure of both cosmetic and functional importance. Cutaneous lesions of the nose occasionally represent a diagnostic challenge and involve the expertise of several specialties from dermatology, otolaryngology—head and neck surgery ...
Hamed Sarikhani, Karena Zhao, Marc A. Polacco, Charles Gropper, Samuel N. Helman   +4 more
doaj   +1 more source