Results 151 to 160 of about 18,028 (178)
Some of the next articles are maybe not open access.

Non Langerhans Cell Histiocytosis of the Rectum: Case Report and Review of the Literature

Japanese Journal of Gastroenterology and Hepatology, 2022
Histiocytosis is a condition resulting from the abnormal proliferation of dentritic cells of the mononuclear phagocytic system. Previously classified as Langerhans cell histiocytosis and non-Langerhans cell histiocytosis, and recently into 5 categories ...
Bouhairie Mm   +3 more
semanticscholar   +1 more source

Uncommon cutaneous non-Langerhans cell histiocytosis arising from dermal dendritic cells in adults: a clinicopathological study of five cases

EJD. European journal of dermatology, 2020
Background Non-Langerhans cell histiocytosis (non-LCH) is a collective term that encompasses a long list of rare “histiocytosis” that do not meet the criteria for Langerhans cell histiocytosis (LCH).
L. Nong   +5 more
semanticscholar   +1 more source

Spontaneous regression of infantile dural-based non-Langerhans cell histiocytosis after surgery: case report.

Journal of Neurosurgery: Pediatrics, 2015
The authors report the case of a large left occipital mass lesion in an 8-month-old boy who presented with seizure. Neuroimaging demonstrated an approximately 5-cm extraaxial tumor, and the patient underwent partial resection.
Yohei Miyake   +3 more
semanticscholar   +1 more source

Erdheim- Chester Disease (Non-Langerhans Cell Histiocytosis)

Journal of Cancer Research Reviews & Reports
52 years old female with recurrent admission for myalgias, inflammatory arthritis, rash around the eyes and abdomen (A, B). Routine blood tests were either normal or negative apart from low C4 level. Pan CT of the body was unremarkable.
Yousef Gulnaz, Adel Ekladious
semanticscholar   +1 more source

Successful treatment of Erdheim-Chester disease, a non-Langerhans-cell histiocytosis, with interferon-alpha.

Blood, 2005
Erdheim-Chester disease is a rare non-Langerhans histiocytosis with multisystem involvement. To date, there is no standard treatment for this disorder, and more than half of the patients succumb within 3 years.
F. Braiteh   +3 more
semanticscholar   +1 more source

A Child with Both Langerhans and Non‐Langerhans Cell Histiocytosis

open access: closedPediatric dermatology, 2002
Ayelet Shani‐Adir   +3 more
openalex   +2 more sources

Benign cephalic histiocytosis progressing into juvenile xanthogranuloma: a non-Langerhans cell histiocytosis transforming under the influence of a virus?

American journal of dermatopathology, 2000
Benign cephalic histiocytosis (BCH) is best understood as a form of non-Langerhans cell histiocytosis, specifically as an early mononuclear variant of juvenile xanthogranuloma (JXG).
R. Rodríguez-Jurado   +2 more
semanticscholar   +1 more source

Progressive nodular histiocytosis – rare variant of cutaneous non‐Langerhans cell histiocytosis

open access: closedJournal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2006
Matthias Lüftl   +3 more
openalex   +2 more sources

[Clinicopathological study of non-Langerhans cell histiocytosis in central nervous system].

Zhonghua nei ke za zhi, 2015
OBJECTIVE To explore the clinicopathological features and imaging characteristics of non-Langerhans cell histiocytosis in central nerve system, thus to facilitate the diagnosis and differential diagnosis.
Tingting Zhang   +4 more
semanticscholar   +1 more source

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