Zobrazeno 1 - 10
of 2 337
pro vyhledávání: '"sinus histiocytosis"'
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Background Rosai-Dorfman Disease (RDD) is a rare self-limiting histiocytosis, more prevalent in children and young adults. It typically manifests as painless bilateral massive cervical lymphadenopathy but may also extend to extra-nodal sites
Externí odkaz:
https://doaj.org/article/7f7fd6a8241a479f93bc1e96bb243699
Publikováno v:
Online Journal of Health & Allied Sciences, Vol 23, Iss 2 (2024)
Background: Rosai-Dorfman disease (RDD), or Sinus histiocytosis with massive lymphadenopathy, is a rare idiopathic disorder characterized by histiocytic proliferation. While lymph node involvement is predominant, extranodal manifestations pose diagno
Externí odkaz:
https://doaj.org/article/7b454f21a1a048f1a4ee26bfefdcaa5f
Autor:
Hamid Nasrollahi, Susan Andalibi, Mansour Ansari, Maral Mokhtari, Ehsan Mohammad Hosseini, Mina Foroughi, Arman Sourani
Publikováno v:
Clinical Case Reports, Vol 12, Iss 6, Pp n/a-n/a (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‐
Externí odkaz:
https://doaj.org/article/81814184bf324cdeb4bfeebed7127b9d
Publikováno v:
JEADV Clinical Practice, Vol 2, Iss 3, Pp 662-665 (2023)
Externí odkaz:
https://doaj.org/article/0280c8c1346441a5adf0f3b9c6d9f641
Publikováno v:
Journal of Dentistry, Vol 24, Iss 2, Pp 256-261 (2023)
Rosai Dorfman disease is generally defined as a massive bilateral painless cervical lymphadenopathy accompanied with both fever and leukocytosis with neutrophilia. Additionally, it may possibly be associated with polyclonal hypergammaglobulinemia, re
Externí odkaz:
https://doaj.org/article/dcdfc161672049d8be7d305d45b62195
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
South African Journal of Radiology, Vol 27, Iss 1, Pp e1-e6 (2023)
Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented. T2W hypointense signal of the soft tissue masses was a di
Externí odkaz:
https://doaj.org/article/e094cef30a6544fcb7f8ff3ec5b2ae28
Publikováno v:
Diagnostic Pathology, Vol 18, Iss 1, Pp 1-5 (2023)
Abstract Background Rosai-Dorfman disease (RDD) is a rare, non-Langerhans cell histiocytosis of unknown etiology. we report a very rare case of recurrent central nervous system RDD with KRAS gene mutation and review the literature to improve our unde
Externí odkaz:
https://doaj.org/article/a528e99ffee94da9b4ba60060a591ee6
Publikováno v:
Clinical Dermatology Review, Vol 7, Iss 1, Pp 80-83 (2023)
Rosai–Dorfman disease (RDD) is a rare, benign idiopathic, non-Langerhans cell histiocytosis. The most common presentation is massive bilateral painless lymphadenopathy with fever and weight loss. Approximately 40% of patients with RDD have extranod
Externí odkaz:
https://doaj.org/article/822dc79601e9445087074e46ec84fc8b
Publikováno v:
Tomography, Vol 8, Iss 6, Pp 2839-2843 (2022)
Background Rosai-Dorfman disease (RDD), the massive lymphadenopathy characterized by the proliferation of sinus histiocytosis, is a relatively idiopathic benign disease with unknown etiology. We reported a rare case of thymic RDD detected by 18F-FDG
Externí odkaz:
https://doaj.org/article/05904dd1f7154dc085a7a521682c9074