Results 121 to 130 of about 10,817 (231)

A Rare Case of Erdheim-Chester Disease (Non-Langerhans Cell Histiocytosis) with Concurrent Langerhans Cell Histiocytosis: A Diagnostic and Therapeutic Challenge

Case Reports in Hematology, 2018
Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocyte disorder most commonly characterized by multifocal osteosclerotic lesions of the long bones demonstrating sheets of foamy histiocyte infiltrates on biopsy with or without histiocytic ...
Hamza Hashmi, Drew Murray, John Greenwell, Marwan Shaikh, Soumit Basu, Maxwell Krem   +5 more
doaj   +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
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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

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

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

Treatment of Langerhans Cell Histiocytosis

, 1996
Histiocytosis X patients present with a variety of clinical manifestations and outcomes. The principal difficulty in the establishment of a definite protocol for treatment is based on the poor understanding of the basic nature of this disease, the ...
김현우, 신규호
core  

Langerhans cell histiocytosis

, 2000
Langerhans cell histiocytosis (LCH) is a rare disorder affecting predominantly children and manifesting as bone pains, bony swellings and lytic lesions. Involvement of vertebrae as presenting manifestation is unusual.
Agarwal, V., Nityanand, S.
core   +1 more source

Visual Dermatologic Case Report: Juvenile Xanthogranuloma of the Labia Majora in a Pediatric Patient. [PDF]

Case Rep Pediatr
Frasier K, Gottesman SP, Shah PR.
europepmc   +1 more source

Case Report Juvenile xanthogranuloma developing after treatment of Langerhans cell histiocytosis: case report and literature review

, 2012
: The synchronous or metachronous development of Langerhans cell histiocytosis and non-Langerhans cell histiocytosis in the same patient is rare. To date, only seven cases of xanthogranulomas developing in young patients with a history of Langerhans cell
Klaus-Daniel Stachel, Abbas Agaimy, Johanna D Strehl, Arndt Hartmann   +3 more
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