Results 111 to 120 of about 10,193 (191)

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

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

Histiocitosis de células de Langerhans con manifestaciones multisistémicas en periodo neonatal

, 2011
We report an unusual case of mediastinal abcessed mass, with involvement of the lung, thymus and probably bone and hematopoietic system, in a newborn that was diagnosed with Langerhans cell histiocytosis.
Martínez, Gloria, Meza, Ivonne, Pasaje, Donaldo, Díaz Castro, Rosalba, Ruiz Tendero, Germán, Días-Castro, Rosalba, Meza, Ivonne Alejandra, Cruz, Claudia Elena, Ruiz, Germán, Ortíz, Alex   +9 more
core  

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

An 11‐Month‐Old Infant With Unusual Diaper Dermatitis

JEADV Clinical Practice, Volume 5, Issue 2, Page 731-733, June 2026.
Majda Chaoui, Léo‐Paul Secco, Ifigenia Spanoudi‐Kitrimi   +2 more
wiley   +1 more source

Synovial Non-langerhans Cell Histiocytosis of the Shoulder: A Case Report and Review of the Literature. [PDF]

J Orthop Case Rep, 2020
Huri G, Çetik RM, Gedikoğlu G, Garbis N.   +3 more
europepmc   +1 more source

Disseminated non-Langerhans cell histiocytosis with an IRF2BP2-NTRK1 gene fusion identified by next-generation sequencing. [PDF]

JAAD Case Rep, 2020
Chan WH, Shah A, Bae G, Hambro C, Martin BA, Brown R, Novoa R, Kwong BY.   +7 more
europepmc   +1 more source

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., Stelten, Bianca M.L., Verrips, Aad, Bianca M.L. Stelten, Wevers, Ron A., Ron A. Wevers, van der Knaap, Marjo S., Verrips, A., Wevers, R.A.   +11 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

Plenary Abstracts Session & Oral Presentations

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source