Results 121 to 130 of about 14,204,460 (231)

A Case of Multisystemic Langerhans Cell Histiocytosis in an Adult

, 2011
Langerhans cell histiocytosis is a rare disease in adults with a myriad of clinical presentations. A case of multisystemic Langerhans cell histiocytosis with involvement of bone, skin, lungs, and the hypothalamic-pituitary-axis is reported.
Chiaw Ling Chng MBBS, MRCP
core   +1 more source

Langerhans Cell Histiocytosis (Letterer-Siwe disease ) - Report of a case

, 2011
Langerhans cell histiocytosis is a rare disorder that occurs when there aretoo many of type of white blood cell called a Langerhans cell. We describe a3-months infant girl who developed wide spread skin lesions since she was 4days of age. . The diagnosis
BS Elagraa, Elagraa, BS, El Hassan, AM, MA Abdulla, SI Ayed, Ayed, SI, Abdulla, MA, AM El Hassan   +7 more
core   +1 more source

Erdheim–Chester Disease Manifesting Without Long Bone Involvement

Respirology Case Reports
Erdheim–Chester Disease (ECD) is an extremely rare, non‐Langerhans cell histiocytosis characterised by the proliferation of foamy histiocytes infiltrating various organs.
Dhiran Sivasubramanian, Karthick Balasubramanian, Mohamed Raghib Hussain Mohamed Kalifa, Sathwik Sanil, Smrti Aravind, Nithish Nanda Palanisamy, Virushnee Senthilkumar   +6 more
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

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

Endocrine manifestations in Langerhans cell histiocytosis.

, 2007
Langerhans cell histiocytosis is a rare, multisystem disease that shows a particular predilection for hypothalamo-pituitary axis involvement. Diabetes insipidus is the most frequent permanent consequence of Langerhans cell histiocytosis, developing in ...
Chrousos, GP, Grossman, AB, Kaltsas, GA, Makras, P, Alexandraki, KI   +4 more
core   +1 more source

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

Generalized indeterminate cell histiocytosis successfully treated with methotrexate

JAAD Case Reports, 2022
Erina Lie, MD, Jaroslaw Jedrych, MD, Ronald Sweren, MD, Michelle L. Kerns, MD   +3 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  

An atypical immunophenotype in generalized eruptive histiocytosis: a case report of coexisting scattered S-100 positivity and seropositivity for Anti-nRNP/Sm antibodies. [PDF]

Front Immunol
Du X, Pu S, Zhu R, Guo D.
europepmc   +1 more source