Results 41 to 50 of about 1,427 (174)
Persistent Cutaneous Papules and Nodules in a Six-year-old Child: A Quiz
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
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
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
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
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
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
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
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
Sinus Histiocytosis with Massive Lymphadenopathy (Rosai Dorfman Disease) of the Liver Masquerading as a Metastatic Malignancy [PDF]
Jacob Sheba SK, Krishnan Elankumaran
openalex +1 more source
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

