Results 61 to 70 of about 1,868 (215)
The 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
Sinus histiocytosis with massive lymphadenopathy. Fifteen new casesd [PDF]
Cancer, 1976 Fifteen cases of chronic lymphadenitis with massive hemophagocytic sinus histiocytosis were analyzed. Fourteen patients were whites, 13 were Europeans, and 11 were males; 10 patients were under 10, 4 were over 20, and 2 over 60 years old. The oldest patient died; all other either healed without therapy or are in excellent condition.
F, Lampert, K, Lennert
openaire +2 more sources
EPSTEIN-BARR-VIRUS ASSOCIATED SYNDROMES IN IMMUNOSUPPRESSED LIVER-TRANSPLANT RECIPIENTS - CLINICAL PROFILE AND RECOGNITION ON ROUTINE ALLOGRAFT BIOPSY [PDF]
, 1990 The clinical profile and histopathologic changes in needle biopsies of the liver were studied in 10 cases of acute Epstein-Barr virus infection occurring in liver transplant recipients.
DEMETRIS, AJ +3 more
core +1 more source
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 +2 more
doaj
Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report
Clinical 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
Extranodal Rosai-Dorfman Disease with Cutaneous and Periodontal Involvement: A Rare Presentation
Case 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
Case of Rosai — Dorfman Disease in a Child
Zdorovʹe Rebenka, 2014 Sinus histiocytosis with massive lymphadenopathy is rare in children. The article describes a case of Rosai — Dorfman disease in 3-year-old boy. The emergence of lymphadenopathy, mainly cervical one, with synchronous lesion of extranodal area — spleen ...
S.V. Vesyoly +6 more
doaj +1 more source
Bagaimana Prognosis Histiocytosis? Sebuah Laporan Kasus [PDF]
, 2013 Penderita histiocytosis dengan keterlibatan multiorgan dan disertai gangguan fungsi organ mempunyai prognosis buruk dan tingkat mortalitas tinggi. Dilaporkan seorang penderita histiocytosis, usia 1 tahun 1 bulan yang datang dengan kelainan di kulit ...
Lestari, R. D. (Rini) +1 more
core
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) — imaging manifestations of renal involvement [PDF]
, 2014 A 23-year-old lady presented with abdominal fullness and distension as well as large abdominal masses in physical exam. Upon ultrasonographic evaluation, two large space occupying lesions anterior to kidneys, with no clear distinction from renal tissue ...
Gholamrezanezhad, Ali +2 more
core +2 more sources
Clinical 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