Intracranial Rosai-Dorfman disease with the petroclival and parasellar involvement mimicking multiple meningiomas: A case report and review of literature
C Wang, P Kuang, F Xu, L Hu - Medicine, 2019 - journals.lww.com
Interventions: The patient received subtotal resection because multiple lesions were
extensive. Outcomes: The vision diminution recovered well after the surgery but the hearing …
extensive. Outcomes: The vision diminution recovered well after the surgery but the hearing …
Rosai–Dorfman disease of the central nervous system: A clinical, radiological, and prognostic study of 12 cases
X Zhang, W Yin, Y Guo, Y He, Z Jiang, Y Li… - Frontiers in …, 2022 - frontiersin.org
Background Rosai–Dorfman disease (RDD) is a rare benign non-Langerhans cell histiocytic
proliferative disease. RDD with central nervous system (CNS) involvement (CNS-RDD) is …
proliferative disease. RDD with central nervous system (CNS) involvement (CNS-RDD) is …
[HTML][HTML] Rosai-Dorfman disease mimicking images of meningiomas: two case reports and literature review
RT Tatit, PEAZ Raffa, GC de Almeida Motta… - Surgical neurology …, 2021 - ncbi.nlm.nih.gov
Background: Rosai-Dorfman disease (RDD) is a rare non-Langerhans cell histiocytic
proliferative disorder classically as a massive cervical lymphadenopathy. However, over the …
proliferative disorder classically as a massive cervical lymphadenopathy. However, over the …
Intracranial Rosai-Dorfman disease involving the cavernous sinus: a case report and review of the literature
Z Li, C Zhou, G Chen, Y Bao - World Neurosurgery, 2018 - Elsevier
Background Rosai-Dorfman disease (RDD), also called sinus histiocytosis with massive
lymphadenopathy, is an idiopathic, non-neoplastic, lymphoproliferative disorder …
lymphadenopathy, is an idiopathic, non-neoplastic, lymphoproliferative disorder …
Isolated intracranial Rosai-Dorfman disease: case report and review of the literature
MA Boissaud-Cooke, K Bhatt, DA Hilton, S Muquit - World neurosurgery, 2020 - Elsevier
Background Rosai-Dorfman disease (RDD) is a rare idiopathic benign proliferative disorder
of histiocytes, predominantly affecting the lymph nodes. RDD can also present in extranodal …
of histiocytes, predominantly affecting the lymph nodes. RDD can also present in extranodal …
Orbital masses as a rare presentation of Rosai-Dorfman disease: Clinicopathologic characterization of five cases
T Steidl, L Li, PD Langer, RE Turbin, JM Gross… - Annals of Diagnostic …, 2024 - Elsevier
Rosai-Dorfman disease (RDD) is a rare, non-Langerhans cell histiocytosis. Most cases
present with marked, non-tender lymphadenopathy due to the proliferation of atypical …
present with marked, non-tender lymphadenopathy due to the proliferation of atypical …
[HTML][HTML] Hypofractionated Radiation Therapy for Subcutaneous Rosai-Dorfman Disease: A Case Report
Rosai-Dorfman disease (RDD) is a rare, heterogeneous, non-Langerhans type histiocytosis.
Local treatment can be recommended for symptomatic patients with unifocal or limited …
Local treatment can be recommended for symptomatic patients with unifocal or limited …
Steroid responsive cavernous sinus syndrome due to Rosai-Dorfman disease: beyond Tolosa-Hunt syndrome–a case report
PR Nóbrega, PGB Rodrigues, I de Sousa Pereira… - BMC neurology, 2021 - Springer
Abstract Background The term “Tolosa-Hunt syndrome”(THS) has been used to refer to
painful ophthalmoplegia associated with nonspecific inflammation of the cavernous sinus …
painful ophthalmoplegia associated with nonspecific inflammation of the cavernous sinus …
[HTML][HTML] Rosai-Dorfman disease of cranial and spinal origin-A case series
Background: Rosai-Dorfman disease (RDD) is an idiopathic nonneoplastic
lymphadenopathy disorder which is characterized by lymph node enlargement, but it may …
lymphadenopathy disorder which is characterized by lymph node enlargement, but it may …
[HTML][HTML] A giant invasive parasagittal meningioma with recurrent seizures in a young female: a case report and review of literature
SA Richard, S Zheng, X Xuehua, C Bowen… - Interdisciplinary …, 2019 - Elsevier
Introduction Parasagittal meningiomas (PM) are very common intracranial lesion but their
occurrence in young adult is very rare. Most giant PM are characterized with the invasion of …
occurrence in young adult is very rare. Most giant PM are characterized with the invasion of …