Results 51 to 60 of about 4,871,906 (169)

Rosai-Dorfman disease with pulmonary involvement mimicking bronchogenic carcinoma

Journal of Cardiothoracic Surgery, 2020
Background Rosai-Dorfman disease is a histiocytic lesion that affects lung rarely. Case presentation We present a 52-year-old female diagnosed with right intrabronchial mass invading the bronchial wall and the extrabronchial tissues with lymphadenopathy.
Haneen Al-Maghrabi, Ahmed Elmahrouk, Maun Feteih, Ahmed Jamjoom, Jaudah Al-Maghrabi   +4 more
doaj   +1 more source

Novel treatment options for subglottic stenosis in Rosai-Dorfman disease: A case report and review of the literature

Otolaryngology Case Reports, 2022
Rosai-Dorfman disease is a rare non-Langerhans cell histiocytosis which classically presents with cervical lymphadenopathy. Extranodal disease in the head and neck is uncommon.
Melissa M. Liu, Sintawat Wangsiricharoen, Shumon I. Dhar   +2 more
doaj   +1 more source

The 2025 ATS/ERS update of the international multidisciplinary classification of the interstitial pneumonias: implications for the pathologist

Histopathology, Volume 89, Issue 3, Page 403-425, September 2026.
This review highlights changes relevant to pathologists in the updated multidisciplinary classification of interstitial pneumonias. Changes include expansion beyond idiopathic disease, subclassification as interstitial (fibrotic vs non‐fibrotic) and alveolar filling disorders, expansion to include additional patterns (e.g.
Andrew G Nicholson, Wendy A. Cooper, Aurelie Fabre, William Travis, Lida P. Hariri, Ayodeji Adegunsoye, Sara Piciucchi, Christopher J Ryerson   +7 more
wiley   +1 more source

Isolated cerebral Rosai–Dorfman disease presenting as a sole mass protruding into the fourth ventricle: A case report

Radiology Case Reports, 2021
Rosai–Dorfman disease is a non–Langherans cell histiocytosis typically revealed by a lymphadenopathy. Central nervous system involvement is rare, exceptionally isolated, and usually consists of dural masses mimicking meningioma.
Guillaume Friconnet, MD, Mathilde Duchesne, MD, PhD, Marcel Gueye, MD, François Caire, MD, PhD, Charbel Mounayer, MD, PhD, Jean-François Emile, MD, PhD, François Labrousse, MD, PhD, Aymeric Rouchaud, MD, PhD   +7 more
doaj   +1 more source

Bilateral breast Rosai‐Dorfman disease screen detected by mammography

Clinical Case Reports, 2023
Rosai‐Dorfman disease (RDD) is a proliferative disorder of histiocytes typically found in nodal sites and commonly observed in females. Patients often present with systemic symptoms such as fever, lymphadenopathy, and weight loss.
Christina Sumner, Karma Salem, Luma Abunimer, Abdulwahab Ewaz, Linsheng Zhang, Ashley Monsrud, Nabil Calisi   +6 more
doaj   +1 more source

Chronic Pruritic Papular Eruption in an Elderly Man

JEADV Clinical Practice, EarlyView.
Filipe Monteiro, Inês Tribolet‐Abreu, Gustavo Almeida‐Silva, Inês Amaral, Ivânia Soares, Sónia Fernandes, Joana Antunes   +6 more
wiley   +1 more source

Rosai-Dorfman disease manifesting as a solitary mass with fat in the thymus a case report

Journal of Cardiothoracic Surgery
Background Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a rare, self-limiting disease that predominantly affects children and young adults. Moreover, the disease is characterized by painless bilateral cervical
Dan Liu, Xia Liu, Yi Sha Liu, Chao Xin Zhou   +3 more
doaj   +1 more source

Outcome of treatment with trametinib in adults with histiocytic neoplasms in the United Kingdom

British Journal of Haematology, Volume 209, Issue 2, Page 747-754, August 2026.
Trametinib (MEK inhibitor) shows efficacy in refractory and high‐risk adult histiocytic neoplasms. At a median follow‐up of 21.4 months, the clinical response rate was 81% (30/37) and the radiological response was 68% (25/37) (n = 37).
Rodothea Amerikanou, Talha Munir, Kristian Bowles, Christopher McNamara, Nikesh Chavda, Elizabeth Price, Jagdish Adiyodi, Alasdair Coles, Philippa Kelsey, Jeffery Smith, Richard Adams, Hayder Hussein, Rui Zhao, Trung Nguyen, Matthew Collin, Satyen Gohil   +15 more
wiley   +1 more source

Glomeruloid haemangioma in Erdheim–Chester disease: An atypical skin manifestation associated with elevated vascular endothelial growth factor‐A levels

British Journal of Haematology, Volume 209, Issue 2, Page 755-759, August 2026.
Glomeruloid haemangiomas and extensive angiomas occurred in a small subset of Erdheim–Chester disease patients, all showing markedly elevated vascular endothelial growth factor‐A (VEGF‐A) levels despite the absence of POEMS (polyneuropathy, organomegaly, M‐spike, and skin disease) syndrome.
Jerome Razanamahery, Matthias Papo, Francesco Pegoraro, Felix Blaison, Paul Legendre, Valentin Carado, Martin Caretti, Aubriot Lorton Marie Helene, Jean‐Francois Emile, Augusto Vaglio, Julien Haroche   +10 more
wiley   +1 more source

Diagnosis of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) by fine needle aspiration cytology

Journal of Cytology, 2009
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare benign disease of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma.
Kushwaha Rashmi, Ahluwalia Charanjeet, Sipayya Varuna   +2 more
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