Rhabdoid glioblastoma: a recently recognized subtype of glioblastoma

详细信息    查看全文

• 作者：Shao-Ching Chen (1) (2)
  Diego Shih-Chieh Lin (2) (3)
  Cheng-Chia Lee (1) (2)
  Sheng-Che Hung (2) (4)
  Yi-Wei Chen (2) (5)
  Sanford P. C. Hsu (1) (2)
  Chun-Fu Lin (1) (2)
  Tai-Tong Wong (2) (6)
  Min-Hsiung Chen (1) (2)
  Hsin-Hung Chen (1) (2)
  
• 关键词：Rhabdoid glioblastoma ; Wilm鈥檚 tumor ; Brain tumor surgery
• 刊名：Acta Neurochirurgica
• 出版年：2013
• 出版时间：August 2013
• 年：2013
• 卷：155
• 期：8
• 页码：1443-1448
• 全文大小：482KB
• 参考文献：1. Beckwith JBPN (1978) Histopathology and prognosis of Wilms' tumors: results from the First National Wilms' Tumor Study. Cancer 41:1937鈥?948 CrossRef
  2. Fung K-M, Perry A, Payner TD, Shan Y (2004) Rhabdoid glioblastoma in an adult. Pathology 36:585鈥?87 CrossRef
  3. He M-XMX, Wang JJJJ (2011) Rhabdoid glioblastoma: case report and literature review. Neuropathol Off J Japan Soc Neuropathol 31:421鈥?26 CrossRef
  4. Kleinschmidt-DeMasters BK, Alassiri AH, Birks DK, Newell KL, Moore W, Lillehei KO (2010) Epithelioid versus rhabdoid glioblastomas are distinguished by monosomy 22 and immunohistochemical expression of INI-1 but not claudin 6. Am J Surg Pathol 34:341鈥?54 CrossRef
  5. Kleinschmidt-DeMasters BKB, Meltesen LL, McGavran LL, Lillehei KOKO (2006) Characterization of glioblastomas in young adults. Brain Pathol (Zurich, Switzerland) 16:273鈥?86 CrossRef
  6. Lath RR, Unosson DD, Blumbergs PP, Stahl JJ, Brophy BPBP (2003) Rhabdoid glioblastoma: a case report. J Clin Neurosci 10:325鈥?28 CrossRef
  7. Lutterbach JLJ, Koch D, Madlinger A, Frommhold H, Pagenstecher A (2001) Atypical teratoid/rhabdoid tumors in adult patients: case report and review of the literature. J Neurooncol 52:49鈥?6 CrossRef
  8. Momota HH, Iwami KK, Fujii MM, Motomura KK, Natsume AA, Ogino JJ, Hasegawa TT, Wakabayashi TT (2011) Rhabdoid glioblastoma in a child: case report and literature review. Brain Tumor Pathology 28:65鈥?0 CrossRef
  9. Mutou J, Hirose Y, Ikeda E, Yoshida K, Nakazato Y, Kawase T (2011) Malignant brain tumor with rhabdoid features in an adult. Neurol Med Chir 51:449鈥?54 CrossRef
  10. Nagai S, Kurimoto M, Ishizawa S, Hayashi N, Hamada H, Kamiyama H, Endo S (2009) A rare astrocytic tumor with rhabdoid features. Brain Tumor Pathol 26:19鈥?4 CrossRef
  11. Perry AFC, Judkins AR (2005) INI1 expression is retained in composite rhabdoid tumors, including rhabdoid meningiomas. Mod Pathol 18:951鈥?58 CrossRef
  12. Rorke LBPR, Biegel JA (1996) Central nervous system atypical teratoid/rhabdoid tumours of infancy and childhood: definition of an entity. J Neurosurg 85:56鈥?5 CrossRef
  13. Wyatt-Ashmead J, Kleinschmidt-DeMasters BK, Hill DA, Mierau GW, McGavran L, Thompson SJ, Foreman NK (2001) Rhabdoid glioblastoma. Clin Neuropathol 20:248鈥?55
  
• 作者单位：Shao-Ching Chen (1) (2)
  Diego Shih-Chieh Lin (2) (3)
  Cheng-Chia Lee (1) (2)
  Sheng-Che Hung (2) (4)
  Yi-Wei Chen (2) (5)
  Sanford P. C. Hsu (1) (2)
  Chun-Fu Lin (1) (2)
  Tai-Tong Wong (2) (6)
  Min-Hsiung Chen (1) (2)
  Hsin-Hung Chen (1) (2)
  
  1. Department of Neurosurgery, Neurological Institute, Taipei Veterans General Hospital, 17F, No. 201, Shih-Pai Road, Sec. 2, Peitou, Taipei, 11217, Taiwan, Republic of China
  2. School of Medicine, National Yang-Ming University, Taipei, Taiwan, Republic of China
  3. Department of Pathology, Taipei Veterans General Hospital, Taipei, Taiwan, Republic of China
  4. Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan, Republic of China
  5. Department of Cancer Tumor Center, Taipei Veterans General Hospital, Taipei, Taiwan, Republic of China
  6. Department of Surgery, Cheng Hsin General hosital, Taipei, Taiwan, Republic of China
  

文摘

Background Rhabdoid glioblastoma is a rare type of recently described malignant brain tumor. It is characterized by a glioblastoma associated with rhabdoid components. Methods Here we report two cases of rhabdoid glioblastoma and a brief literature review. The first patient was a 19-year-old boy who initially presented with a foul-smelling odor and progressive right-side weakness. The second case was a 29-year-old male patient who presented only with a severe headache. Results Both of these patients were young, and the disease progression was quick despite optimal treatment. Conclusion The diagnosis of rhabdoid glioblastoma was confirmed after microscopic and immunohistochemical findings.