Results 111 to 120 of about 4,903,700 (215)

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

Solitary Langerhans cell histiocytosis of the hard palate: a diagnostic pitfall

, 2016
Langerhans cell histiocytosis (LCH) is a relatively rare and unique disease characterized by an abnormal proliferation of immature dendritic cells. It is predominantly seen in children with adults showing less than ten times the incidence compared to ...
Varsha, Dalal, Varsha, D, Siraj, Fouzia, Kaur, M, Kaur, Manveen, Chaudhary, N, Siraj, F, Chaudhary, Neena   +7 more
core   +1 more source

Intestinal Langerhans cell histiocytosis presenting with symptoms similar to inflammatory bowel disease: a case report

Pathology and Oncology Research
Background:Langerhans cell histiocytosis is a rare disease characterized by the abnormal proliferation of Langerhans cells within a single organ or multiple organs.
Yuqing Liu, Zhenwei Chen, Lu Wang, Baizhou Li   +3 more
doaj   +1 more source

Paediatric Langerhans cell histiocytosis with diabetes insipidus: remarkable recovery journey

Journal of the Pakistan Medical Association
A rare condition known as Langerhans cell histiocytosis (LCH) is characterised by the clonal growth of dendritic cells called Langerhans cells, which play a significant role in the immune system. A diverse range of clinical presentations are probable as
Versha Rani Rai, Zulqarnain Buriro, Roshia Parveen, Mohsina Noor, Heeranand Rathore   +4 more
doaj   +1 more source

Langerhans cell histiocytosis: case report

, 2021
Langerhans cells are dendritic cells seen above the basal layer of squamous epithelia. They are cells specialized in the capture of antigens and in the induction of T lymphocyte responses.
Siqueira, Edllanckar dos Santos
core  

A Case of Langerhans Cell Histiocytosis Presenting with Suprasellar Mass and Panhypopituitarism Clinic

Langerhans cell histiocytosis (LCH) is a rare disease involving multiple systems, and it is caused by excessive proliferation of Langerhans cells. The hypothalamic-pituitary region (HPR) is involved in 5%-50% of all LCH patients, particularly those with ...
Murat Şahin, Emek Topuz, Dilek Tüzün, Nursel Yurttutan   +3 more
core   +1 more source

A case of diagnosis and treatment of mediastinal Langerhans cytosis

Journal of Cardiothoracic Surgery
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, Lei Xian, Yi Wang, Yourong Chen, Yifei Lu, Daying Liang   +5 more
doaj   +1 more source

Langerhans cell histiocytosis in monocygote twins: case reports.

, 1996
Langerhans cell histiocytosis includes three clinical forms of histiocytosis X. We describe a disseminated form of Langerhans cell histiocytosis (Letterer-Siwe disease) in monozygotic twins.
Mader I, Stock KW, Steinbrich W, Radue EW   +3 more
core   +1 more source

Langerhans Cell Histiocytosis [PDF]

Ear, Nose & Throat Journal, 2010
Sandra, Camelo-Piragua, Eduardo, Zambrano, Liron, Pantanowitz   +2 more
openaire   +2 more sources

Unusual Neurological Manifestation of Langerhans Cell Histiocytosis in an Adult

Ear, Nose & Throat Journal
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, Ines Kharrat MD, Youssef Hbaieb MD, Mariam Ben Ayed MD, Malek Mnejja MD, Bouthaina Hammami MD, Basma Souissi MD, Ilhem Charfeddine MD   +7 more
doaj   +1 more source