Results 21 to 30 of about 24,931 (232)

ALK-Positive Histiocytosis with Peripheral Blood Histiocytes: A Case Report

, 2020
Histiocytoses are a diverse group of rare, clinically heterogeneous disorders characterised by tissue infiltration of histiocytes, which may result in organ dysfunction and failure.
Williams, Bronwyn, Barbaro, Pasquale, Swain, Fiona, Bronwyn Williams, Fiona Swain, Pasquale Barbaro   +5 more
core   +1 more source

A frontal lobe mass in a 6-year-old girl. [PDF]

Brain Pathol
Brain Pathology, EarlyView.
Vacca FS, Mochizuki A, Patel SK, Jones B, Roy S, Gupta K.   +5 more
europepmc   +2 more sources

Adult Langerhans cell histiocytosis presenting with multisystem involvement and sarcomatoid features: a case report

Journal of Medical Case Reports, 2020
Background Langerhans cell tumors are rare clonal disorders characterized by neoplastic proliferation of dendritic cells that can be further classified into the subtypes Langerhans cell histiocytosis and Langerhans cell sarcoma, which are rare neoplasms ...
Luis E. Aguirre, Ingrid Schwartz, Jennifer Chapman, Marcelo F. Larsen, Alvaro Alencar   +4 more
doaj   +1 more source

Intermediate-dose cytarabine is an effective therapy for adults with non-Langerhans cell histiocytosis

Orphanet Journal of Rare Diseases, 2022
Background Non-Langerhans cell histiocytosis, including Erdheim–Chester disease (ECD), Rosai–Dorfman disease (RDD), indeterminate cell histiocytosis (ICH), and unclassified histiocytosis, is a rare disorder lacking a standard treatment strategy.
Ting Liu, Hua-cong Cai, Hao Cai, Miao Chen, Wei Zhang, Jian Li, Dao-bin Zhou, Xin-xin Cao   +7 more
doaj   +1 more source

Indeterminate dendritic cell tumor (IDCT) [PDF]

Vestnik Dermatologii i Venerologii, 2023
Indeterminate dendritic cell tumor (IDCT) is rare histiocytic tumor characterized by the proliferation of indeterminate dendritic cells. It is more often diagnosed in middle-aged people, in approximately equal proportions in men and women.
Evgenia V. Okladnikova, Vladimir M. Merk, Yuriy А. Krivopalov, Vladimir А. Khorzhevskii, Tatiana G. Ruksha   +4 more
doaj   +1 more source

Clinical features and treatment outcomes of langerhans cell histiocytosis: A nationwide survey from Korea histiocytosis working party

, 2021
Langerhans cell histiocytosis; outcome; permanent consequence ...
유은선, 유경하
core   +1 more source

Swelling of bilateral parotid glands: An unusual symptom of multisystem Langerhans cell histiocytosis

SAGE Open Medical Case Reports, 2014
Objective: Langerhans cell histiocytosis is an unusual disorder of unknown etiology with heterogeneous clinical behaviors and variable outcomes. It can involve one or more organs or systems, but to our best knowledge, parotid glands involvement in ...
Xiaojun Yuan, Mengjie Tang, Qi Sheng, Xiaodong Zhu, Qin Zhang   +4 more
doaj   +1 more source

Puzzle histiocytosis (solitary mononuclear xanthogranuloma with LCH component). A case report*

, 2017
We report a case of 40-year-old Caucasian man presented with an asymptomatic nodule localized on his arm. The puzzle histiocytosis composed of juvenile xanthogranuloma and Langerhans cell histiocytosis was diagnosed.
Katarzyna Woszczyna-Mleczko, Andrzej Marszałek, Artur Kowalik, Agnieszka Harazin-Lechowska, Piotr Bobkiewicz, Janusz Ryś   +5 more
core   +1 more source

Manganese overload as a co-factor of neurological symptoms in a patient with sclerosing cholangitis due to Langerhans cell histiocytosis

Haematologica
Not available.
Jerome Razanamahery, Ahmed Idbaih, Matthias Papo, Fabien Robelin, Jean-Francois Emile, Sylvain Audia, Bernard Bonnotte, Julien Haroche   +7 more
doaj   +1 more source

Hand-Schüller-Christian disease

Indian Journal of Dental Research, 2012
Langerhan cell histiocytosis, formerly known as histiocytosis X, traditionally denotes a group of diseases that stem from proliferative reticuloendothelial disturbances.The etiology and pathogenesis of the disease remain debatable.
Deepak Bhargava, Kalyani Bhargava, Vinay Hazarey, Sindhu Milind Ganvir   +3 more
doaj   +1 more source