Results 61 to 70 of about 18,630 (199)

Erdheim-Chester Disease: Utility of 18F-FDG Positron Emission Tomography [PDF]

Journal of Clinical and Diagnostic Research, 2018
Erdheim-Chester Disease (ECD) is a rare non Langerhans cell histiocytosis of unknown origin with multiorgan involvement. We report a case of a man who presented to us with haematuria, asthenia, fever, nausea and malleolar oedema.
Angelina Cistaro, Maria Licari, Simone Margotti, Daniele Penna, Vincenzo Arena   +4 more
doaj   +1 more source

Langerhans cell histiocytosis in children: a case report and brief review of the literature

PAMJ Clinical Medicine, 2019
Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, is a non-malignant disease involving clonal proliferation of Langerhans cells. It is an orphan disease affecting mainly the child and the young adult.
Zakaria El Ouali, Nisrine Khoubila, Siham Cherkaoui, Mohamed Rachid, Mouna Lamchahab, Meryem Qachouh, Abdellah Madani, Asmaa Quessar   +7 more
doaj   +1 more source

Dermoscopy in the diagnosis of juvenile xanthogranuloma [PDF]

Anais 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, Roberto Gomes Tarlé, Lismary Aparecida de Forville Mesquita   +2 more
doaj   +1 more source

Diffuse plane xanthomas as the first manifestation of multiple myeloma

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Eleni Koutra, Elke Lusmöller, Hosam Ghanem, Astrid Aumann, Jens Atzpodien, Rudolf Stadler   +5 more
wiley   +1 more source

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

BMC 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, Bernhard Zelger, Gisela Schweigmann, Barbara Brunner, Bettina Zelger, Gabriele Kropshofer, Ursula Kiechl-Kohlendorfer   +6 more
doaj   +1 more source

Strawberry Gingivitis as the Primary Sign of ANCA‐Negative Granulomatosis With Polyangiitis (GPA): A Case Report

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Wegener's granulomatosis (WG) could be a lethal disease if not diagnosed and managed timely. Oral involvement is rare and often presents as gingival hyperplasia with a traditional “strawberry gingivitis” appearance. Dental practitioners may be the first ones to encounter WG and may be able to prevent disease progression like the present case ...
Samaneh Salari, Zahra Mirfeizi, Amir Moeintaghavi, Toktam Zamani, Hanieh Shayegan Majd   +4 more
wiley   +1 more source

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

Case 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, Hania Shakeri, Niloofar Nobakht, Anjay Rastogi, Mohammad Kamgar   +4 more
doaj   +1 more source

Kimura Disease With Eosinophilic Granulomatosis With Polyangiitis Successfully Treated by Mepolizumab

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Diagnosis of Kimura's disease should be considered if a middle‐aged Asian male patient presents with painless enlargement of cervical lymph nodes, eosinophilia, and elevated serum total IgE level. Patients with Kimura's disease can have concurrent EGPA or presentations consistent with EGPA.
Wei Du, Ranran Dai, Xiaoyan Chen, Wei Tang   +3 more
wiley   +1 more source

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

Case 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, Alok Mohanty, Lisa J. Kohler, Howard J. Meyerson   +3 more
doaj   +1 more source

Clinical features and outcomes of non-pulmonary unifocal adult Langerhans cell histiocytosis [PDF]

, 2022
Marie Hu, Gaurav Goyal, Jithma P. Abeykoon, Aldo A. Acosta‐Medina, Gordan J. Ruan, Jason R. Young, Aishwarya Ravindran, N. Nora Bennani, Mithun Vinod Shah, Robert Vassallo, Jay H. Ryu, Caroline Davidge‐Pitts, Matthew J. Koster, W. Oliver Tobin, Julio C. Sartori‐Valinotti, Karen L. Rech, Ronald S. Go   +16 more
openalex   +1 more source