Central nervous system involvement in Rosai-Dorfman disease: Report of a case with a review of the literature

被引:0
作者
Shuangshoti, S
Navalitloha, Y
Sukpanichnant, S
Unhasuta, C
Shuangshoti, S
机构
[1] Chulalongkorn Univ, Fac Med, Dept Pathol, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Fac Med, Dept Surg, Bangkok 10330, Thailand
[3] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Pathol, Bangkok, Thailand
关键词
central nervous system; massive lymphadenopathy; Rosai-Dorfman disease; sinus histiocytosis;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A 55-year-old woman had Rosai-Dorfman disease (RDD) forming multiple masses of abnormal histiocytes, three in the cranial cavity and one in the left orbit that was proptotic, The masses were removed and found to consist of abnormal histiocytes that were immunoreactive to cluster designation 68 (CD68) (KP-1), alpha-1-antitrypsin and S-100 protein and showed emperipolesis. A review of 28 cases of RDD, including this instance, revealed a ratio of 5:2 between males and females and a mean age of 32 years. Intracranial involvement was much more frequent than that of the spinal cord. Histologically, central nervous system (CNS) RDD must be distinguished from meningioma, Langerhans cell histiocytosis, and plasma cell granuloma, Surgical extirpation appears to be the treatment of choice for this idiopathic histiocytic proliferative disorder of the CNS in comparison with radiotherapy and steroid treatment, which have also been tried.
引用
收藏
页码:341 / 346
页数:6
相关论文
共 50 条
  • [21] Isolated Intracranial Rosai-Dorfman Disease: Case Report and Review of the Literature
    Boissaud-Cooke, Matthew A.
    Bhatt, Kush
    Hilton, David A.
    Muquit, Samiul
    WORLD NEUROSURGERY, 2020, 137 : 239 - 242
  • [22] Isolated intracranial Rosai-Dorfman disease: A case report and literature review
    Triana-Perez, A. B.
    Sanchez-Medina, Y.
    Perez-Del Rosario, P. A.
    Millan-Corada, A. M.
    Gomez-Perals, L. F.
    Dominguez-Baez, J. J.
    NEUROCIRUGIA, 2011, 22 (03): : 255 - 260
  • [23] Recurrent central nervous system Rosai-Dorfman disease with KRAS mutation: a case report
    Qingyang Wang
    Hongxiang Ren
    Liyuan Zheng
    Juan Wang
    Dingrong Zhong
    Diagnostic Pathology, 18
  • [24] Rosai-Dorfman Disease of the Spine: A Case Report of a Rare Disease and Review of the Literature
    Bahauddin, Rabia
    Al-Taie, Alaa
    Al-Khafaji, Fatima
    Barah, Ali
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2022, 14 (06)
  • [25] Rosai-Dorfman disease of the maxilla: A rare case report and literature review
    Nagai, Takahiro
    Yamazaki, Manabu
    Nishikawa, Atsushi
    Kodama, Yasumitsu
    Nishiyama, Hideyoshi
    Hayashi, Takafumi
    Tanuma, Jun-ichi
    Takagi, Ritsuo
    Tomihara, Kei
    JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY MEDICINE AND PATHOLOGY, 2022, 34 (05) : 665 - 671
  • [26] Intracranial Rosai-Dorfman disease with the petroclival and parasellar involvement mimicking multiple meningiomas A case report and review of literature
    Wang, Chao
    Kuang, Pingding
    Xu, Fangfang
    Hu, Ling
    MEDICINE, 2019, 98 (18)
  • [27] Rosai-Dorfman disease of vertebra: Case report and literature review
    Igrutinovic, Zoran
    Medovic, Rasa
    Markovic, Slavica
    Kostic, Gordana
    Raskovic, Zorica
    Tanaskovic-Nestorovic, Jelena
    Radovanovic, Marija
    Vuletic, Biljana
    TURKISH JOURNAL OF PEDIATRICS, 2016, 58 (05) : 566 - 571
  • [28] Recurrent central nervous system Rosai-Dorfman disease with KRAS mutation: a case report
    Wang, Qingyang
    Ren, Hongxiang
    Zheng, Liyuan
    Wang, Juan
    Zhong, Dingrong
    DIAGNOSTIC PATHOLOGY, 2023, 18 (01)
  • [29] Rosai-Dorfman Disease of Rare Isolated Spinal Involvement: Report of 4 Cases and Literature Review
    Huang, Bo Yuan
    Zhang, Hua
    Zong, Wen Jing
    Sun, Yan Hui
    WORLD NEUROSURGERY, 2016, 85 : 367.e11 - 367.e16
  • [30] A Case of Isolated Central Nervous System Rosai-Dorfman Disease
    Algul, Fatma Ebru
    Erdem, Beguem Y. E. N., I
    Yegen, Guelcin
    Yolbas, Servet
    NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, 2024, 61 (01): : 90 - 93