May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Enlargement of the Pineal Gland in Hereditary Retinoblastoma May Not Indicate Pineoblastoma
Author Affiliations & Notes
  • M.J. Shapiro
    Ophthalmology,
    University of Illinois, Chicago, IL
  • M.T. Duffy
    Ophthalmology,
    University of Illinois, Chicago, IL
  • M.F. Mafee
    Radiology,
    University of Illinois, Chicago, IL
  • D.P. Edward
    Ophthalmology,
    University of Illinois, Chicago, IL
  • Footnotes
    Commercial Relationships  M.J. Shapiro, None; M.T. Duffy, None; M.F. Mafee, None; D.P. Edward, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 3379. doi:
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      M.J. Shapiro, M.T. Duffy, M.F. Mafee, D.P. Edward; Enlargement of the Pineal Gland in Hereditary Retinoblastoma May Not Indicate Pineoblastoma . Invest. Ophthalmol. Vis. Sci. 2005;46(13):3379.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose:To describe benign pineal enlargement (pseudopineoblastoma) after chemotherapy for hereditary retinoblastoma and its differentiation from pineoblastoma. Methods: Case report Results:Two patients with hereditary retinoblastoma underwent chemotherapy and on MRI had significant enlargement of the pineal gland. Initially, the MR findings were diagnosed as pineoblastoma. Despite significant growth, the pineal glands were somewhat smaller and more regular in shape and showed a more homogeneous internal signal than most pineoblastomas. Immediate testing with unenhanced CT showed no calcification. Repeat MRI showed no further growth after 2 months and with serial studies for 1 year in both patients. Pineal cysts were seen at 18 and 30 months using the 3 Tesla MRI. Conclusions: Benign enlargement of the pineal gland may occur after chemotherapy for hereditary retinoblastoma. In cases with uncertain diagnosis, additional testing is important in order to avoid confusion of benign enlargement since the treatment of pineoblastoma is associated with significant morbidity.

Keywords: retinoblastoma • imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • oncology 
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