Results 111 to 120 of about 10,082 (250)

Langerhans cell histiocytosis with oral manifestations: a rare and unusual case report [PDF]

open access: yes, 2012
Langerhans cell histiocytosis (LCH), is a rare, proliferative disorder in which the accumulation of pathologic Langerhans cells leads to local tissue infiltration and destruction.
Agarwal, Manjushree   +2 more
core   +1 more source

Langerhans Cell Histiocytosis Associated With Chronic Myeloid Leukemia: A Pediatric Case Report

open access: yesCancer Reports, Volume 9, Issue 5, May 2026.
ABSTRACT Background Langerhans cell histiocytosis (LCH) is a rare clonal neoplasm driven by activating mutations in the MAPK pathway, leading to accumulation of pathological Langerhans cells in various tissues. LCH is increasingly associated with secondary malignancies, including leukemias, lymphomas, and solid tumors. However, chronic myeloid leukemia
Atbin Latifi, Sina Yousefian
wiley   +1 more source

Altano-axial subluxation with torticollis secondary to Langerhans cell histocytosis

open access: yesInterdisciplinary Neurosurgery, 2017
Langerhans Cell Histiocytosis is a rare disease featuring aberrant proliferation of dendritic cells that can infiltrate the bony skeleton. The authors report a case of six-year-old female presenting with torticollis. She was found to have extensive lytic
Joshua Y. Chua, MD   +5 more
doaj   +1 more source

Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]

open access: yes, 2016
Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco   +4 more
core  

Airway involvement in interstitial lung disease [PDF]

open access: yes, 2006
PURPOSE OF REVIEW: After briefly discussing several ways to approach airway involvement in interstitial lung diseases - by diagnostic methodologies used to assess it, considering different topographical involvement, related to its presence in the diffuse
Robalo-Cordeiro, C
core   +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

Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

open access: yesDermatologica Sinica, 2015
Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis seen most commonly in childhood and adolescence. Extracutaneous involvement is rare. We report an interesting and extremely rare case of systemic (skin, lung, spleen, and colon) “juvenile ...
Hikmet Tekin Nacaroglu   +6 more
doaj   +1 more source

Novel BRAF fusion in Erdheim–Chester disease with pulmonary manifestations: Importance of RNA‐based testing and response to MEK inhibition

open access: yes
Histopathology, EarlyView.
Igor Odintsov   +5 more
wiley   +1 more source

Pulmonary Langerhans Cell Histiocytosis Presenting as Multiple Obstructing Bronchial Lesions and Pulmonary Masses

open access: yesThe Clinical Respiratory Journal, Volume 20, Issue 5, May 2026.
We describe a case of PLCH presenting as multiple obstructing bronchial lesions and pulmonary masses in a 36‐year‐old man. To our knowledge, this is the first report of PLCH presenting as bilateral hilar masses and airway obstructive lesions. ABSTRACT Pulmonary Langerhans cell histiocytosis is a rare lung disease, which was previously classified as ...
Jingyuan Fan   +3 more
wiley   +1 more source

Xanthoma Disseminatum with Tumor-Like Lesion on Face

open access: yesCase Reports in Dermatological Medicine, 2014
Xanthoma disseminatum (XD) is a rare benign mucocutaneous xanthomatosis that is classified as a benign non-Langerhans cell histiocytosis. We report a 62-year-old man who presented with widespread yellow-brown papulonodular and tumoral lesions on face ...
Habib Ansarin   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy