Results 81 to 90 of about 9,884 (233)

Dermoscopy in the diagnosis of juvenile xanthogranuloma [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2018
: Juvenile xanthogranuloma is the most common form of non-Langerhans cell histiocytosis. It manifests clinically as a red-yellow papule, usually showing spontaneous remission. The diagnosis is based on clinical and histological findings.
Thaís Erance de Oliveira   +2 more
doaj   +1 more source

An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]

open access: yes, 2016
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F.   +5 more
core   +2 more sources

MEK Inhibition with Trametinib in Patients with Non-Langerhans Cell Histiocytosis

open access: yesBlood, 2019
Background: Activation of the MAPK pathway through BRAF mutations or other molecular alterations is a hallmark of the non-Lagerhans cell histiocytosis (non-LCH) such Erdheim-Chester disease (ECD) or Rosai-Dorfman disease (RDD). Conventional clinical molecular testing of tumor tissue fails to identify targetable molecular alteration in about one third ...
Filip Janku   +5 more
openaire   +1 more source

Implementing Health‐Related Quality of Life Assessment in Pediatric Oncology: A Feasibility Study

open access: yesPediatric Blood &Cancer, Volume 73, Issue 5, May 2026.
ABSTRACT Background There is growing interest in embedding health‐related quality of life (HRQoL) assessment and patient‐reported outcome measures (PROMs) within clinical cancer care. This study evaluated the feasibility, acceptability, and usability of implementing an electronic PROM (ePROM) platform to measure HRQoL in children with cancer ...
Mikaela Doig   +13 more
wiley   +1 more source

A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening

open access: yes
Brain Pathology, EarlyView.
Alyssa M. Lee   +3 more
wiley   +1 more source

Multiple histiocytic foam cell nodules of the tongue in a Shih Tzu dog

open access: yesVeterinary Record Case Reports, Volume 14, Issue 2, May 2026.
Abstract An uncommon histiocytic lesion of the tongue was described in an 11‐year‐7‐month‐old male Shih Tzu dog that presented with multiple nodules on the upper lip and tongue, with further dissemination on the ventral lingual surface observed during sedation.
Hugo Henrique Rocon Gregório   +4 more
wiley   +1 more source

High viral load of Merkel cell polyomavirus DNA sequences in Langerhans cell sarcoma tissues. [PDF]

open access: yes, 2014
International audienceBACKGROUND: Langerhans cell (LC) sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytologic features and an LC phenotype.
A Kanik   +38 more
core   +4 more sources

A rare cutaneous lesion in the neonatal period: The non-Langerhans cell histiocytosis

open access: yesMarmara Medical Journal, 2020
The non-Langerhans cell histiocytosis (non-LCH) is a group of diseases characterized by cutaneous involvement in the neonatal period. The non-LCH affects less than 1 in 200,000 children born each year. A definitive diagnosis is important for the treatment of the disease.
Adnan BARUTCU   +3 more
openaire   +3 more sources

Perianal Paget's Disease: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Perianal Paget's disease is rare and may be secondary to an underlying anorectal adenocarcinoma. Full‐thickness biopsy with immunohistochemistry is key to distinguish primary from secondary disease and to guide staging. Wide local excision is standard, while radiotherapy is a reasonable option when radical surgery is declined.
Daniela Lira   +5 more
wiley   +1 more source

Erdheim-Chester Disease Presenting with Secondary Hypertension as a Result of Bilateral, Proximal Renal Artery Stenosis: A Case Report

open access: yesCase Reports in Nephrology and Dialysis, 2017
Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis presenting most commonly with bone and central nervous system symptoms, including but not limited to bone pain and diabetes insipidus.
Farid Arman   +4 more
doaj   +1 more source

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