Results 121 to 130 of about 24,068 (238)

Adult langerhans cell histiocytosis

, 2007
Langerhans cell histiocytosis is a group of idiopathic disorders characterized by the abnormal proliferation of specialized bone marrow-derived Langerhans cells. There are one to two cases per million population.
Bahceci, Mithat, Goekalp, Deniz, Tuzcu, Alparslan, Isikdogan, Abdurrahman, Cil, Timucin   +4 more
core   +1 more source

Chronic Ulcer on the Vulva

JEADV Clinical Practice, Volume 5, Issue 3, Page 1010-1012, September 2026.
Farhanaz Panjshiri, Reed Gioe, Carole Bitar   +2 more
wiley   +1 more source

Gastrointestinal involvement in Langerhans' cell histiocytosis (Histiocytosis X): a clinical report of three cases

, 1990
The gastrointestinal tract may be involved in Langerhans' cell histiocytosis, either as part of a generalized disease or as a separate primary entity. Three patients with gastrointestinal involvement are described. One patient presented with a history of
Schipper, M. E., Egeler, R. M., Heymans, H. S.   +2 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

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

Langerhans Cell Histiocytosis Associated With Chronic Myeloid Leukemia: A Pediatric Case Report

Cancer Reports
Background Langerhans cell histiocytosis (LCH) is a rare clonal neoplasm driven by activating mutations in the MAPK pathway, leading to accumulation of pathological Langerhans cells in various tissues.
Atbin Latifi, Sina Yousefian
doaj   +1 more source

Novel BRAF fusion in Erdheim–Chester disease with pulmonary manifestations: Importance of RNA‐based testing and response to MEK inhibition

Histopathology, Volume 89, Issue 3, Page 558-561, September 2026.
Igor Odintsov, Henry D. Tazelaar, Jerry C. Lee, Lloyd E. Damon, Walter Patrick Devine, Kirk D. Jones   +5 more
wiley   +1 more source

Cardiac mass as the primary diagnostic clue of Edheim–Chester disease

Clinical Case Reports
Key Clinical Message We introduced one of the rare causes of intra‐cardiac mass, that is, ECD and a new gene mutation (SLC29A3) that is probably related to this disease, and we noted the importance of using several diagnostic methods to rule out other ...
Azin Alizadehasl, Maryam Mohseni Salehi, Zeinab Soltani, Soudeh Roudbari, Mahsa Akbarian, Somaye Mohebbi, Pegah Salehi   +6 more
doaj   +1 more source

A death from Langerhans cell histiocytosis and tuberculosis in 18th Century Hungary - what palaeopathology can tell us today [PDF]

, 2006
Spigelman, M, Pap, I, Donoghue, HD
core  

Malignant histiocytosis [PDF]

British Journal of Haematology, 1999
openaire   +2 more sources