Results 41 to 50 of about 1,427 (174)

Persistent Cutaneous Papules and Nodules in a Six-year-old Child: A Quiz

open access: yesActa Dermato-Venereologica, 2022
is missing (Quiz)
Jeanette Halskou Haugaard   +3 more
doaj   +1 more source

Tissue‐Resident Myeloid and Histiocytic Cells in Health and Disease: Novel Emerging Concepts

open access: yesAmerican Journal of Hematology, Volume 100, Issue 12, Page 2305-2319, December 2025.
ABSTRACT Although all myeloid cells are considered to derive from hematopoietic stem cells, the cells in each myeloid lineage are heterogeneous populations, and their distribution and functions vary, depending on underlying physiologic and pathologic processes, age, sex, and genetic and epigenetic signatures.
Peter Valent   +27 more
wiley   +1 more source

Multiple Drug Regimen-Refractory Rosai–Dorfman–Destombes Disease Mimicking Relapsing Polychondritis Successfully Treated with Cobimetinib

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2022
Rosai-Dorfman-Destombes disease (RDD) or sinus histiocytosis with massive lymphadenopathy is a rare non-Langerhans cell histiocytosis of unknown cause.
Kima López-Aldabe   +11 more
doaj   +1 more source

Combination of Photodynamic and Bronchoscopic Intervention With Radiation Therapy in Treating Pulmonary Pleomorphic Sarcoma: A Case Report

open access: yesThe Clinical Respiratory Journal, Volume 19, Issue 9, September 2025.
We discuss a case where an innovative combination of photodynamic therapy (PDT) and local radiation therapy to address the diagnostic and therapeutic challenges associated with PPSS resulted in significant improvements in clinical symptoms and patient survival, demonstrating the success of this treatment.
Ran An   +5 more
wiley   +1 more source

Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT This case highlights the possibility that Immunoglobulin G4‐related disease (IgG4‐RD) lesions can also occur in the sternoclavicular joint. If a neoplastic lesion is found in the sternoclavicular joint, a biopsy should be attempted to diagnose IgG4‐RD as a differential.
Remi Mizuta   +18 more
wiley   +1 more source

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

open access: yesJournal 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   +2 more
doaj  

Rosai-Dorfman disease of the colon presented as small solitary polypoid lesion

open access: yesRare Tumors, 2010
Rosai-Dorfman disease (RDD) was formerly known as “sinus histiocytosis with massive lymphadenopathy”, and cases involving the gastrointestinal tract are rare.
Munenori Ide   +8 more
doaj   +1 more source

Extranodal Rosai-Dorfman Disease with Cutaneous and Periodontal Involvement: A Rare Presentation

open access: yesCase Reports in Oncology, 2011
Sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease (RDD) was first described as a distinct clinicopathological entity by Rosai and Dorfman in 1969. SHML is commonly characterized by painless cervical lymphadenopathy, and its
M.J. Molina-Garrido, C. Guillén-Ponce
doaj   +1 more source

Radiotherapeutic outcomes of Rosai–Dorfman disease with falx cerebri and superior sagittal sinus involvement: A rare case report with long‐term follow‐up

open access: yesClinical Case Reports, Volume 12, Issue 6, June 2024.
Key Clinical Message Intracranial RDD is rare medical event mimicking different diagnoses. Although the surgical resection is the best treatment option, but radiation therapy can also achieves long‐term suboptimal outcomes. Abstract An 83‐year‐old male with a history of tension‐type headaches was evaluated.
Hamid Nasrollahi   +6 more
wiley   +1 more source

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