scholarly journals Spinal intramedullary hemangioblastoma and schwannoma collision tumor: illustrative case

2021 ◽  
Vol 1 (3) ◽  
Author(s):  
Matthew T. Neal ◽  
Alexandra E. Richards ◽  
Kara L. Curley ◽  
Kliment Donev ◽  
Mark K. Lyons ◽  
...  

BACKGROUNDIntramedullary spinal cord tumors represent a minority of intradural tumors. Among intramedullary spinal cord tumors, hemangioblastomas are uncommon, and schwannomas are extremely rare. Collision tumors are histologically distinct tumors that are intermingled and growing together.OBSERVATIONSIn this report, the authors describe a patient with a cervical intramedullary collision tumor involving a hemangioblastoma and schwannoma. To the authors’ knowledge, no prior spinal intramedullary collision tumor involving multiple neoplasms has been described. The patient’s presentation and management are described.LESSONSClinicians should consider the possibility of collision tumors when evaluating intramedullary spinal cord tumors, especially when patient presentation and radiographic findings are atypical. When tumors with similar radiographic characteristics form collision tumors, distinction using preoperative imaging can be extremely challenging. In addition, surgical management of intramedullary collision tumors, like that for all intramedullary spinal cord tumors, should involve meticulous perioperative care and a methodical surgical technique. Maximal safe resection will depend upon histopathological diagnosis, anatomical location of the tumor, presence of distinct dissection planes, and stability of neuromonitoring. Finally, ongoing research on the genetics of intramedullary spinal cord tumors may identify underlying genetic links for intramedullary hemangioblastomas and schwannomas.

1986 ◽  
Vol 26 (4) ◽  
pp. 311-317 ◽  
Author(s):  
Toshihiro YASUI ◽  
Akira HAKUBA ◽  
Junsuke KATSUYAMA ◽  
Shuro NISHIMURA

Spinal Cord ◽  
2014 ◽  
Vol 52 (10) ◽  
pp. 769-773 ◽  
Author(s):  
H Arima ◽  
T Hasegawa ◽  
D Togawa ◽  
Y Yamato ◽  
S Kobayashi ◽  
...  

Neurosurgery ◽  
1997 ◽  
Vol 41 (6) ◽  
pp. 1327-1336 ◽  
Author(s):  
Nobu Morota ◽  
Vedran Deletis ◽  
Shlomi Constantini ◽  
Markus Kofler ◽  
Henry Cohen ◽  
...  

2018 ◽  
Vol 31 (3) ◽  
pp. 112-119 ◽  
Author(s):  
Tej D. Azad ◽  
Arjun V. Pendharkar ◽  
Viet Nguyen ◽  
James Pan ◽  
Ian D. Connolly ◽  
...  

2014 ◽  
Vol 56 (2) ◽  
pp. 169-174 ◽  
Author(s):  
Asim F. Choudhri ◽  
Matthew T. Whitehead ◽  
Paul Klimo ◽  
Blake K. Montgomery ◽  
Frederick A. Boop

2008 ◽  
Vol 66 (1) ◽  
pp. 59-63 ◽  
Author(s):  
Mario Augusto Taricco ◽  
Vinicius Monteiro de Paula Guirado ◽  
Ricardo Bragança de Vasconcellos Fontes ◽  
José Pindaro Pereira Plese

BACKGROUND: Primary spinal cord intramedullary tumors are rare and present with insidious symptoms. Previous treatment protocols emphasized biopsy and radiation/chemotherapy but more aggressive protocols have emerged. OBJECTIVE: To report our experience. METHOD: Forty-eight patients were diagnosed with primary intramedullary tumors. The cervical cord was involved in 27% and thoracic in 42% of patients. Complete microsurgical removal was attempted whenever possible without added neurological morbidity. RESULTS: Complete resection was obtained in 33 (71%) patients. Neurological function remained stable or improved in 32 patients (66.7%). Ependymoma was the most frequent tumor (66.7%). CONCLUSION: Neurological outcome is superior in patients with subtle findings; aggressive microsurgical resection should be pursued with acceptable neurological outcomes.


2019 ◽  
Vol 33 (2) ◽  
pp. 198-201
Author(s):  
Hidetoshi Murata ◽  
Mitsuru Sato ◽  
Ryohei Miyazaki ◽  
Takahiro Tanaka ◽  
Hiromasa Abe ◽  
...  

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