Results 91 to 100 of about 38,208 (195)

A case of coexisting Warthin tumor and langerhans cell histiocytosis associated with necrosis, eosinophilic abscesses and a granulomatous reaction in intraparotid lymph nodes

Rare Tumors, 2011
We present a patient (50-year-old male) with coexisting Warthin tumor and involvement of two intraparotid lymph nodes by Langerhans cell histiocytosis associated with necrosis, eosinophilic abscesses and a granulomatous reaction.
Char Loo Tan, Gangaraju Changal Raju, Fredrik Petersson   +2 more
doaj   +1 more source

BRAFV600E-induced senescence drives Langerhans cell histiocytosis pathophysiology

Nature Network Boston, 2021
Camille Bigenwald, Jessica Le Berichel, C. Wilk, Rikhia Chakraborty, Steven T. Chen, Alexandra Tabachnikova, Rebecca Mancusi, H. Abhyankar, M. Casanova-Acebes, I. Laface, Guray Akturk, Jenielle Jobson, Zoi Karoulia, Jerome C. Martin, J. Grout, Anahita Rafiei, Howard Lin, M. Manz, Alessia Baccarini, Poulikos I. Poulikakos, Brian D. Brown, S. Gnjatic, Amaja Lujambio, Kenneth L. McClain, J. Picarsic, Carl E. Allen, Miram Merad   +26 more
semanticscholar   +1 more source

Vinblastine chemotherapy in adult patients with langerhans cell histiocytosis: a multicenter retrospective study

Orphanet Journal of Rare Diseases, 2017
BackgroundVinblastine is the standard treatment for children with Langerhans cell histiocytosis (LCH). Whether this treatment could be extended to adults with LCH is questionable.
A. Tazi, G. Lorillon, J. Haroche, A. Néel, S. Dominique, A. Aouba, J. Bouaziz, Constance de Margerie-Melon, E. Bugnet, V. Cottin, T. Comont, C. Lavigne, J. Kahn, J. Donadieu, S. Chevret   +14 more
semanticscholar   +1 more source

Perifollicular Langerhans cell histiocytosis

Dermatology Online Journal, 2012
A 25-year-old man presented with a 13-year history of an erythematous, papular eruption of his face and trunk, which was treated in the past as acne and psoriasis with isotretinoin and methotrexate, respectively. Histopathologic examination demonstrated an infiltrate of Langerhans cells, which was consistent with Langerhans cell histiocytosis.
Mir, Adnan, Fisher, Max, Kamino, Hideko, Soter, Nicholas A   +3 more
openaire   +4 more sources

Langerhans Cell Histiocytosis of the Clavicle in a 13-Year-Old Boy

Case Reports in Orthopedics, 2014
Langerhans Cell Histiocytosis (LCH) is a rare neoplasm characterized by abnormal proliferation of histiocytic cells. In this case report, we describe a unique case of a 13-year-old boy who presented to the clinic with an insidious onset of mid-clavicular
Shital N. Parikh, Vishal R. Desai, Anita Gupta, Christopher G. Anton   +3 more
doaj   +1 more source

Langerhans cell histiocytosis of the sacrum

Radiology Case Reports, 2014
Langerhans cell histiocytosis is a rare disease with a wide spectrum of clinical presentations. It is a multisystemic disease with organ system involvement ranging from simple-where it involves only one organ-to widespread progressive disease. Although it can affect any age group, the peak incidence is between 1 and 3 years of age.
openaire   +4 more sources

Elderly male patient presenting with jaundice and cholangitis brings an unexpected histopathological finding, case report

Heliyon
In this report, we present a case of the first-time manifestation of Langerhans cell histiocytosis in the biliary tract of a 79-year-old male patient. Cholangiocarcinoma was the suspected diagnosis, based on the patient's painless jaundice.
Gergana Nenova, Dietrich A. Ruess, Sophia Chikhladze, Heiko Becker, Sylvia Timme-Bronsert, Uwe Wittel   +5 more
doaj  

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

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

Poster Sessions

HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source