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Diplopia as presenting sign of Turcot syndrome

VIRGINIE NINCLAUS, SOPHIE WALRAEDT UGent, Edward Baert UGent, Genevieve Laureys UGent, Bart Leroy UGent and JULIE DE ZAEYTIJD (2017) INTERNATIONAL OPHTHALMOLOGY. 37(1). p.275-278
abstract
To describe a patient with diplopia who was diagnosed with Turcot syndrome. A 10-year-old boy presented with a history of left-sided sixth and seventh nerve palsy. He underwent imaging of the brain and colon, a full ophthalmological and genetic work-up. A 10-year-old boy was referred with combined left-sided sixth and seventh nerve palsy since 1 month without symptoms of raised intracranial pressure. BCVA was 6/6 in both eyes. Fundoscopy revealed bilateral, multiple, oval pigmented ocular fundus lesions (POFLs) in the 4 quadrants. These POFLs, together with the cranial nerve palsies raised the suspicion of Turcot syndrome, a familial neoplasia syndrome characterized by familial colorectal cancer and tumours of the central nervous system. Urgent MRI scan of the brain and stereotactic biopsy showed a primitive neuroectodermal tumour (PNET) at the pons. Coloscopy revealed multiple polyps. DNA analysis of the APC gene confirmed the clinical diagnosis of Turcot syndrome. The PNET was treated with combined radio- and chemotherapy. The patient underwent a prophylactic total colectomy as virtually all patients develop a carcinoma of the colorectal region if left untreated. Although strabismus is not, diplopia in childhood is rare and seldom innocuous. It requires a prompt and thorough diagnostic evaluation, including thorough, dilated fundoscopy. The presence of POFLs combined with neurological symptoms suggestive of a brain tumour should alert the clinician of the possibility of Turcot syndrome. Recognition of this rare syndrome can lead to earlier diagnosis, which is vital for appropriate surveillance and early surgical intervention of the highly frequent neoplasias in Turcot Syndrome.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
Turcot syndrome, Diplopia in childhood, APC gene, Pigmented ocular fundus lesions, Familial neoplasia syndrome, Brain tumour, FAMILIAL ADENOMATOUS POLYPOSIS, MUTATIONS
journal title
INTERNATIONAL OPHTHALMOLOGY
Int. Ophthalmol.
volume
37
issue
1
pages
275 - 278
Web of Science type
Article
Web of Science id
000394159800042
ISSN
0165-5701
DOI
10.1007/s10792-016-0246-z
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
7254403
handle
http://hdl.handle.net/1854/LU-7254403
date created
2016-06-16 10:36:47
date last changed
2017-06-01 13:00:26
@article{7254403,
  abstract     = {To describe a patient with diplopia who was diagnosed with Turcot syndrome. 
A 10-year-old boy presented with a history of left-sided sixth and seventh nerve palsy. He underwent imaging of the brain and colon, a full ophthalmological and genetic work-up. 
A 10-year-old boy was referred with combined left-sided sixth and seventh nerve palsy since 1 month without symptoms of raised intracranial pressure. BCVA was 6/6 in both eyes. Fundoscopy revealed bilateral, multiple, oval pigmented ocular fundus lesions (POFLs) in the 4 quadrants. These POFLs, together with the cranial nerve palsies raised the suspicion of Turcot syndrome, a familial neoplasia syndrome characterized by familial colorectal cancer and tumours of the central nervous system. Urgent MRI scan of the brain and stereotactic biopsy showed a primitive neuroectodermal tumour (PNET) at the pons. Coloscopy revealed multiple polyps. DNA analysis of the APC gene confirmed the clinical diagnosis of Turcot syndrome. The PNET was treated with combined radio- and chemotherapy. The patient underwent a prophylactic total colectomy as virtually all patients develop a carcinoma of the colorectal region if left untreated. 
Although strabismus is not, diplopia in childhood is rare and seldom innocuous. It requires a prompt and thorough diagnostic evaluation, including thorough, dilated fundoscopy. The presence of POFLs combined with neurological symptoms suggestive of a brain tumour should alert the clinician of the possibility of Turcot syndrome. Recognition of this rare syndrome can lead to earlier diagnosis, which is vital for appropriate surveillance and early surgical intervention of the highly frequent neoplasias in Turcot Syndrome.},
  author       = {NINCLAUS, VIRGINIE and WALRAEDT, SOPHIE and Baert, Edward and Laureys, Genevieve and Leroy, Bart and DE ZAEYTIJD, JULIE},
  issn         = {0165-5701},
  journal      = {INTERNATIONAL OPHTHALMOLOGY},
  keyword      = {Turcot syndrome,Diplopia in childhood,APC gene,Pigmented ocular fundus lesions,Familial neoplasia syndrome,Brain tumour,FAMILIAL ADENOMATOUS POLYPOSIS,MUTATIONS},
  language     = {eng},
  number       = {1},
  pages        = {275--278},
  title        = {Diplopia as presenting sign of Turcot syndrome},
  url          = {http://dx.doi.org/10.1007/s10792-016-0246-z},
  volume       = {37},
  year         = {2017},
}

Chicago
NINCLAUS, VIRGINIE, SOPHIE WALRAEDT, Edward Baert, Genevieve Laureys, Bart Leroy, and JULIE DE ZAEYTIJD. 2017. “Diplopia as Presenting Sign of Turcot Syndrome.” International Ophthalmology 37 (1): 275–278.
APA
NINCLAUS, V., WALRAEDT, S., Baert, E., Laureys, G., Leroy, B., & DE ZAEYTIJD, J. (2017). Diplopia as presenting sign of Turcot syndrome. INTERNATIONAL OPHTHALMOLOGY, 37(1), 275–278.
Vancouver
1.
NINCLAUS V, WALRAEDT S, Baert E, Laureys G, Leroy B, DE ZAEYTIJD J. Diplopia as presenting sign of Turcot syndrome. INTERNATIONAL OPHTHALMOLOGY. 2017;37(1):275–8.
MLA
NINCLAUS, VIRGINIE, SOPHIE WALRAEDT, Edward Baert, et al. “Diplopia as Presenting Sign of Turcot Syndrome.” INTERNATIONAL OPHTHALMOLOGY 37.1 (2017): 275–278. Print.