Results 91 to 100 of about 9,611 (207)

A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]

open access: yes, 2015
Introduction The histiocytoses are a group of clinically diverse diseases distinguished from one another based on the specific immunophenotype of the lesional cells, implying derivation from the same precursor cell.
Barros, MS, Guilherme   +5 more
core   +2 more sources

Recurrent Pneumothorax Revealing Lymphangioleiomyomatosis in a Young Woman: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Lymphangioleiomyomatosis (LAM) should be considered in young women presenting with recurrent pneumothorax. Early diagnosis through high‐resolution computed tomography(HRCT)and histopathological analysis is essential for timely management and improved patient outcomes.
Qihang Zhang   +3 more
wiley   +1 more source

The various clinical spectra of juvenile xanthogranuloma: imaging for two case reports and review of the literature

open access: yesBMC Pediatrics, 2019
Background Juvenile xanthogranuloma (JXG) belongs to the heterogeneous group of non-Langerhans cell histiocytosis and is caused by an accumulation and proliferation of macrophages.
Michaela Höck   +6 more
doaj   +1 more source

Erdheim-Chester Disease Associated with Marginal Zone Lymphoma and Monoclonal Proteinemia

open access: yesCase Reports in Hematology, 2011
Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis. We report a fatal case of ECD with extensive cardiac involvement associated with a marginal zone lymphoma and monoclonal proteinemia in a young man.
Peter G. Pavlidakey   +3 more
doaj   +1 more source

Flat Topped Brown Papules on a Four-Year-Old Male

open access: yesRevista da Sociedade Portuguesa de Dermatologia e Venereologia, 2020
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Francisca Alves   +3 more
doaj   +1 more source

Erdheim-Chester Disease: a comprehensive review of the literature [PDF]

open access: yes, 2013
Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. Individuals affected by this disease are typically adults between their 5th and 7th decades of life. Males and females are almost equally affected.
Mirra Manevich-Mazor   +2 more
core   +1 more source

Rosai–Dorfman Disease, Presenting as a Mass in the Trachea: A Case Report

open access: yesRespirology Case Reports, Volume 13, Issue 12, December 2025.
We present a rare case of Rosai–Dorfman disease (RDD) confined solely to the trachea. After initial bronchoscopic resection, systemic corticosteroid therapy was initiated due to lesion progression, successfully stabilizing the disease for 4 years. ABSTRACT A 45‐year‐old woman was referred to our clinic for evaluation of a 17 mm tracheal mass detected ...
Taeho Youn   +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

Thoracic, abdominal and musculoskeletal involvement in Erdheim-Chester disease: CT, MR and PET imaging findings. [PDF]

open access: yes, 2014
BACKGROUND: Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis with characteristic radiological and histological features. This entity is defined by a mononuclear infiltrate consisting of lipid-laden, foamy histiocytes that stain
Antunes, C, Donato, P, Graça, B
core   +1 more source

A case of canine cutaneous reactive histiocytosis over the body trunk in an adult pit bull terrier

open access: yesVeterinary Record Case Reports, Volume 13, Issue 4, December 2025.
Abstract The objective of this report is to present a case of canine cutaneous reactive histiocytosis with a high number of dendritic cells. A 7‐year‐old male pit bull terrier was presented with a 5‐month history of skin nodules and plaques on the trunk of varying diameter, along with corneal oedema and anterior uveitis.
Ioanna Papadogiannaki   +3 more
wiley   +1 more source

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