Automated Author Profile

C.E., Francis

Current S-Index

1.7

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.9

Average Dataset Index per dataset

Total Datasets

2

Total datasets for this author

Average FAIR Score

88.5%

Average FAIR Score per dataset

Total Citations

2

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

Supplementary Material for: A cavernous sinus meningioma in a child with progressive bilateral visual loss ultimately attributed to unsuspected optic nerve sheath meningiomas

Introduction: Pediatric optic nerve sheath meningiomas (ONSMs) are rare in children and have an aggressive presentation in the pediatric population often resulting in rapid vision decline. Here, we report a case of right cavernous sinus meningioma (CSM) with delayed diagnosis of concomitant bilateral ONSM, ultimately leading to permanent bilateral blindness. Case presentation: A 7-year-old boy with a history of right trochlear nerve palsy and amblyopia presented with worsening right eye vision. An MRI revealed a right CSM that was resected however the patient experienced progressive visual acuity decline from 20/60 right eye and 20/40 left eye to light perception right eye and 20/400 left eye, along with bilateral optic atrophy appreciated on optical coherence tomography. Repeat evaluation of the brain MRIs revealed bilateral ONSM characterized by a tram-track appearance. Visual acuity remained unimproved 3 years after optic canal decompression with optic nerve sheath fenestration followed by proton beam radiation.Conclusion: Pediatric ONSM is rare, with high risk of permanent blindness in children. Intracranial meningioma and unexplained painless vision loss should prompt careful evaluation of orbital neuroimaging for this condition.

Authors

  • karger, figshare admin ;
  • D.X., Wang ;
  • C.S., Walker ;
  • Y.A., Ahmedin ;
  • M.A., Ohan ;
  • N.A., Vitanza ;
  • R.P., Ermoian ;
  • E.E., Crotty ;
  • C.E., Francis ;
  • M.T., Cabrera
1 Citation0 Mentions88% FAIR0.9 Dataset Index
10.6084/m9.figshare.307998172025

Supplementary Material for: A cavernous sinus meningioma in a child with progressive bilateral visual loss ultimately attributed to unsuspected optic nerve sheath meningiomas (Version: 1)

Introduction: Pediatric optic nerve sheath meningiomas (ONSMs) are rare in children and have an aggressive presentation in the pediatric population often resulting in rapid vision decline. Here, we report a case of right cavernous sinus meningioma (CSM) with delayed diagnosis of concomitant bilateral ONSM, ultimately leading to permanent bilateral blindness. Case presentation: A 7-year-old boy with a history of right trochlear nerve palsy and amblyopia presented with worsening right eye vision. An MRI revealed a right CSM that was resected however the patient experienced progressive visual acuity decline from 20/60 right eye and 20/40 left eye to light perception right eye and 20/400 left eye, along with bilateral optic atrophy appreciated on optical coherence tomography. Repeat evaluation of the brain MRIs revealed bilateral ONSM characterized by a tram-track appearance. Visual acuity remained unimproved 3 years after optic canal decompression with optic nerve sheath fenestration followed by proton beam radiation.Conclusion: Pediatric ONSM is rare, with high risk of permanent blindness in children. Intracranial meningioma and unexplained painless vision loss should prompt careful evaluation of orbital neuroimaging for this condition.

Authors

  • karger, figshare admin ;
  • D.X., Wang ;
  • C.S., Walker ;
  • Y.A., Ahmedin ;
  • M.A., Ohan ;
  • N.A., Vitanza ;
  • R.P., Ermoian ;
  • E.E., Crotty ;
  • C.E., Francis ;
  • M.T., Cabrera
1 Citation0 Mentions88% FAIR0.9 Dataset Index
10.6084/m9.figshare.30799817.v12025