Zobrazeno 1 - 10
of 3 754
pro vyhledávání: '"Rosai Dorfman disease"'
Autor:
Luther B. Adair, II, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 4809-4813 (2024)
An uncommon benign histiocytic illness, Rosai-Dorfman disease (RDD) mostly affects lymph nodes but can also manifest as extranodal involvement. We describe a case of a female patient, sixty years of age, who had joint discomfort, sleeplessness, weigh
Externí odkaz:
https://doaj.org/article/898f85a2cf8d47afb66f51acfc855729
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-7 (2024)
Abstract Background Rosai–Dorfman disease (RDD)/sinus lymphohistiocytosis is a rare benign lymphoproliferative disorder. Only 25% show extra-nodal manifestation, only 5% are seen involving the CNS, with intraventricular manifestation rarely reporte
Externí odkaz:
https://doaj.org/article/e721e29e6fd04e50a1eb5d175dcc6141
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 67, Iss 3, Pp 641-644 (2024)
Histiocytic disorders mostly occur as de-novo nodal or extranodal benign masses with rare secondary malignant transformation. A 10-year-old female presented with 10-cm cervical swelling since 9 months associated with fever. Computed tomography reveal
Externí odkaz:
https://doaj.org/article/4caaadb571614f1785df34eb2d7a611d
Autor:
Dragomira Nikolova, Aleksandar Yordanov, Aleksandra Maslarova, Radka Hristoskova, Vera Damyanova, Savina Hadjidekova, Atanas Radinov
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 38, Iss 1 (2024)
Rosai-Dorfman (RDD) is a rare histiocytic syndrome with variable clinical characteristics and extranodal involvement in more than 43% of the patients. This mini-review presents an overview of the literature on Rosai-Dorfman disease. The histological
Externí odkaz:
https://doaj.org/article/7d9b90f254ee4b63827cbb930c54701e
Autor:
Dayuan Liu, Ning Li, Yubo Zhu, Yunxiang Zhong, Guolong Deng, Mingfa Wang, Caicai Zhang, Jigao Feng
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundRosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy (SHML), is a rare benign disorder characterized by the proliferation of histiocytes of uncertain origin. Central nervous system (CNS) involvement, particularly
Externí odkaz:
https://doaj.org/article/39245bb85cec422d80c7a32e7f7f1d01
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-5 (2024)
Abstract Background Rosai-Dorfman disease (RDD), known as sinus histiocytosis with massive lymphadenopathy, commonly involves lymph nodes in the neck or mediastinum, although extranodal involvement is observed in approximately 40% of RDD patients. RD
Externí odkaz:
https://doaj.org/article/caec8a3e80de47c49b11727a438e20f5
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-8 (2024)
Abstract Neurologic Rosai–Dorfman disease (RDD) is a rare type of non-Langerhans cell histiocytosis that affects the central nervous system. Most neurologic RDDs grow like meningiomas, have clear boundaries, and can be completely resected. However,
Externí odkaz:
https://doaj.org/article/7ade09dea14942908e3df31e2e93137a
Autor:
V. G. Potapenko, D. S. Abramov, V. V. Baykov, T. L. Grigorieva, M. S. Selinkina, L. O. Nikolskaya, J.-F. Emile
Publikováno v:
Онкогематология, Vol 19, Iss 2, Pp 46-55 (2024)
Rosai–Dorfman disease is the most frequent variant of non-Langerhans cell histiocytosis. Local forms can be resected or irradiated. If the process involves multiple organs, systemic chemotherapy can cure some patients. This article includes literat
Externí odkaz:
https://doaj.org/article/0bc85939f3a44ecd89631a05b86cb997
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-4 (2024)
Abstract 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 bilat
Externí odkaz:
https://doaj.org/article/5e525937e6d54f1586b00778d662a761
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