Results 81 to 90 of about 11,417 (249)

Nasal and Nasopharyngeal Rosai-Dorfman Disease

Journal of the Belgian Society of Radiology, 2022
Teaching Point: Nasal and nasopharyngeal Rosai-Dorfman disease is a rare cause of nasal obstruction.
Kelly Di Dier, M. Lemmerling, G. De Vos
semanticscholar   +1 more source

Think highly of immunoglobulin G4‐related chronic rhinosinusitis as a clinical entity in immunoglobulin G4‐related disease

Eye &ENT Research, Volume 2, Issue 3, Page 151-163, September 2025.
Abstract IgG4‐related chronic rhinosinusitis (IgG4‐related CRS) is gaining recognition among various specialized physicians. As a systemic disease involving multiple organs, IgG4‐related CRS is still not widely recognized as an independent clinical entity. Given the complexity of diagnosing autoimmune‐related multisystem diseases, early recognition and
Lianqi Wan, Luo Zhang, Yingshi Piao, Yuan Zhang   +3 more
wiley   +1 more source

Case series of volar juvenile xanthogranuloma: Clinical observation of a peripheral rim of hyperkeratosis [PDF]

, 2014
Juvenile xanthogranuloma is a benign histiocytic tumor predominantly occurring in children as yellowish papules on the head and trunk. Presentations on the volar surfaces are rare and may cause diagnostic confusion with pyogenic granuloma, eccrine poroma
Amadi, Ugochukwu, Do, Thy Thy, Ha Lan, Thanh T., Hristov, Alexandra, Khandpur, Ritika, Maier, Lisa, Mervak, Julie, Wang, Frank   +7 more
core   +1 more source

Rosai-Dorfman disease

Saudi Medical Journal, 2022
Objectives: To document the clinicopathological features of Rosai-Dorfman disease (RDD) at 2 tertiary hospitals in the western region of Saudi Arabia. Methods: We retrieved all cases diagnosed as RDD at King Abdulaziz University Hospital and King Faisal ...
J. Al-Maghrabi
semanticscholar   +1 more source

Morphological, immunohistochemical and molecular analysis of follicular dendritic cell sarcomas: L1CAM as a new diagnostic marker

Histopathology, Volume 87, Issue 2, Page 258-269, August 2025.
Pathohistological analysis of FDCS revealed a morphological spectrum and led to the identification of the adhesion molecule L1CAM as a novel diagnostic immunomarker for FDCS. Sequencing identified NFKBIA as the most frequently altered gene, of note, exclusively in cases with a predominant epithelioid cytomorphology.
Selina Schelbert, Katja Maurus, Sabine Roth, German Ott, Katrin S Kurz, Carolin Mogler, Barbara Wollenberg, John Linde, Alberto Zamo, Ioannis Anagnostopoulos, Susanne Gramlich, Andreas Rosenwald, Elena Gerhard‐Hartmann   +12 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

Spinal Rosai–Dorfman disease: Case report of a rare disorde

The Egyptian Journal of Radiology and Nuclear Medicine, 2015
Background: Rosai–Dorfman disease (sinus histiocytosis with massive lymphadenopathy (SHML)) is a rare, histiocytic, lymphoproliferative disease of unknown etiology affecting young people with male predominance.
A. Elsotouhy, M. Abozed, A. Marioud, A. Haider, A. Roux   +4 more
doaj   +1 more source

Rosai Dorfman Disease: A Rare Cause of Cervical Lymphadenopathy [PDF]

National Journal of Laboratory Medicine, 2018
Rosai Dorfman disease, a sinus histiocytosis, is rare to find and difficult to diagnose. It may masquerade as commoner diseases including infections and malignancies.
Sreenath Sreenivasan, Kiren George Koshy, Santhosh Kumar TS, Jasen Joseph, T Anuvind   +4 more
doaj   +1 more source

Extranodal (cutaneous) Rosai Dorfman: a rare presentation [PDF]

, 2017
Rosai Dorfman disease is a rare histiocytic disorder of unknown etiology commonly involving the cervical lymph nodes first described in 1969, Extranodal involvement is very rare.
Ghodake, Nishant, Khadatkar, Ashwini
core   +2 more sources

Case report: BRAF-inhibitor therapy in BRAF-mutated primary CNS tumours including one case of BRAF-mutated Rosai-Dorfman disease [PDF]

, 2022
Christopher Cronin, Ronan Andrew McLaughlin, Louise Lane, Francesca M. Brett, Michael Jansen, Niamh Bermingham, Gerald Wyse, Liam Grogan, Patrick G. Morris, Séamus O’Reilly   +9 more
openalex   +1 more source