Results 131 to 140 of about 23,888 (239)

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
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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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Langerhans Cell Histiocytosis and Other Histiocytic Lesions

Head and Neck Pathology
Histiocytoses, including Langerhans cell histiocytosis (LCH), comprise a diverse group of histiocytic disorders characterized by the abnormal accumulation and proliferation of histiocytes in various tissues or organs throughout the body, ranging from ...
Reed A. McKinney, Guanghua Wang
semanticscholar   +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
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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.
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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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Extensive reactive cutaneous histiocytic infiltrate resembling non-Langerhans cell histiocytosis as the presenting sign of underlying vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome. [PDF]

JAAD Case Rep
Wang CX, Yokoyama CC, Rosman IS, Musiek AC.   +3 more
europepmc   +1 more source