Movatterモバイル変換


[0]ホーム

URL:


Journal Logo

Email to Colleague

Colleague's E-mail is Invalid

Your Name:
Colleague's Email:
Separate multiple e-mails with a (;).
Message:

Your message has been successfully sent to your colleague.



Some error has occurred while processing your request. Please try after some time.

Export to

CLINICAL STUDIES

Diagnosis and Management of Pineocytomas

Deshmukh, Vivek R. M.D.; Smith, Kris A. M.D.; Rekate, Harold L. M.D.; Coons, Stephen M.D.; Spetzler, Robert F. M.D.

Author Information

Division of Neurological Surgery, Barrow Neurological Institute, St. Joseph’s Hospital and Medical, Center, Phoenix, Arizona

Division of Neurological Surgery, Barrow Neurological Institute, St. Joseph’s Hospital and Medical, Center, Phoenix, Arizona

Division of Neurological Surgery, Barrow Neurological Institute, St. Joseph’s Hospital and Medical, Center, Phoenix, Arizona

Division of Neuropathology, Barrow Neurological Institute, St. Joseph’s Hospital and Medical, Center, Phoenix, Arizona

Division of Neurological Surgery, Barrow Neurological Institute, St. Joseph’s Hospital and Medical, Center, Phoenix, Arizona

Reprint requests: Robert F. Spetzler, M.D., c/o Neuroscience Publications, Barrow Neurological Institute, 350 West Thomas Road, Phoenix, AZ 85013-4496. Email:[email protected]

Received, August 18, 2003.

Accepted, March 24, 2004.

Neurosurgery55(2):p 349-357, August 2004. |DOI:10.1227/01.NEU.0000129479.70696.D2

Abstract

OBJECTIVE: 

Pineocytomas are associated with the most favorable prognosis of all pineal tumors. However, a subset of pineocytomas may have a predilection for recurrence and therefore behave aggressively.

PATIENTS AND METHODS: 

Records of nine patients (five men, four women; mean age, 44 yr; range, 24–63 yr) with histologically diagnosed pineocytomas consecutively treated between 1990 and 2003 were reviewed retrospectively to identify factors predictive of aggressiveness. Eight patients presented with hydrocephalus and four with tectal compression. Three patients underwent gross total resection, and six underwent subtotal resection or biopsy.

RESULTS: 

Three local recurrences necessitated reoperation. One recurrence involved the obex of the fourth ventricle. The mean time to recurrence was 3.5 years (range, 1–7 yr). There was no correlation between histological features and tumor recurrence. Patients undergoing radiosurgery showed stable or attenuated local disease (mean follow-up, 19.3 mo; range, 6–36 mo). Mean radiographic follow-up was 34 months (range, 6 mo to 10 yr). Mean clinical follow-up was 36 months (range, 1 mo to 10 yr).

CONCLUSION: 

A subset of pineocytomas demonstrates the potential for symptomatic recurrence. We advocate an attempt at gross total tumor resection for all symptomatic patients with tectal plate compression, reserving radiosurgery for small, subtotally resected, or recurrent lesions. Patients must be followed closely for recurrence. Radiosurgery seems to be beneficial for local tumor control. Further investigation is needed to identify histological markers for pineocytomas that behave aggressively.

Copyright © by the Congress of Neurological Surgeons

You can read the full text of this article if you:

Log InAccess through Ovid

Source

Neurosurgery55(2):349-357, August 2004.
Email to Colleague

Colleague's E-mail is Invalid

Your Name:
Colleague's Email:
Separate multiple e-mails with a (;).
Message:

Your message has been successfully sent to your colleague.



Some error has occurred while processing your request. Please try after some time.


[8]ページ先頭

©2009-2025 Movatter.jp