Results 61 to 70 of about 9,189,306 (207)

Endocrine Implications of Thyroid Incidentalomas Detected During Lymphoma Staging With 18F‐Fluorodeoxyglucose Positron Emission Tomography

Clinical Endocrinology, Volume 103, Issue 4, Page 605-611, October 2025.
ABSTRACT Objective This study investigated the prevalence, characteristics, and endocrine implications of thyroid incidentalomas detected during lymphoma staging using FDG‐PET/CT. Design Retrospective cohort study. Patients A total of 795 adult patients with lymphoma who underwent FDG‐PET/CT for staging at a tertiary oncology centre were included ...
Marcos Tadashi Kakitani Toyoshima, Roberta Morgado Ferreira Zuppani, Isabelle Pinheiro Amaro, Camila Regina Pereira Batista de Macedo, Ricardo Miguel Costa de Freitas, Rodrigo Dolphini Velasques, Juliana Pereira, Rafael Loch Batista, Debora Lúcia Seguro Danilovic, Delmar Muniz Lourenço Jr., Ana O. Hoff   +10 more
wiley   +1 more source

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

Perforating Colitis Secondary to Immune Checkpoint Inhibitor Use in a Patient With Pericolonic Involvement by Rosai-Dorfman Disease

ACG Case Reports Journal, 2022
Recently, the use of immunotherapy has increased substantially for the treatment of several malignancies. It is associated with several gastrointestinal adverse events; however, severe complications such as intestinal perforation are rare.
Ahmed M. Bakhshwin, J. Robertson, Mrinal Sarwate, Daniel E. Roberts   +3 more
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

Rosai-Dorfman disease of the oral cavity

Autopsy and Case Reports, 2023
First described by J Rosai and R F Dorfman in 1969, Rosai-Dorfman disease (RDD) is a benign, self-limiting histiocytosis of unknown etiology. It is usually seen in the first two decades of life.
Abir Charfeddine, Mounir Omami, Marwa Garma, Ahlem Bellalah, Sameh Sioud, Jamil Selmi   +5 more
doaj  

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

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