SS – OCT angiography in macular dystrophies

Purpose To assess the ability of swept source optical coherence tomography angiography (SS – OCT‐A) to identify abnormalities of the retinal and choroidal vascular network in macular dystrophies. Methods Optical coherence tomography angiography and structural OCT were performed using a Swept‐source...

Full description

Saved in:
Bibliographic Details
Published in:Acta ophthalmologica (Oxford, England) Vol. 95; no. S259
Main Authors: El Matri, L., Falfoul, Y., El Matri, K., Hassairi, A., Maamouri, R., Chebil, A.
Format: Journal Article
Language:English
Published: Malden Wiley Subscription Services, Inc 01.09.2017
Subjects:
ISSN:1755-375X, 1755-3768
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Purpose To assess the ability of swept source optical coherence tomography angiography (SS – OCT‐A) to identify abnormalities of the retinal and choroidal vascular network in macular dystrophies. Methods Optical coherence tomography angiography and structural OCT were performed using a Swept‐source DRI OCT Triton (Topcon, Corporation, Japan) for patients with Stargardt disease, Best maculopathy, pseudo‐vitelliform dystrophy and progressive cone dystrophy. In our series, for every patient the clinical diagnosis was confirmed by the results of molecular genetic study. Results In Stargardt patients, we found alterations especially located at the level of the deep capillary plexus and choriocapillaris. There were different degrees of choriocapillaris impairment, with no residual choriocapillaris inside area of retinal epithelium pigment atrophy in advanced stages. Large choroidal vessels and borders of the atrophy were well visualized. In patients with Best maculopathy and pseudo‐vitelliform dystrophy, OCT‐A revealed neovascularisation in the outer retina and the choriocapillaris while traditional multimodal imaging wasn't conclusive. In progressive cone dystrophy, there was a retinal vasculature signal reduction in both superficial and deep plexus associated with window effect in the outer retina and the choriocapillaris due to the retinal and RPE atrophy. Conclusions In inherited macular distrophies, OCT‐A may provide information of great interest. In stargardt disease, OCT‐A findings were in agreement with the results suggesting primitive severe involvement of choriocapillaris. In Best maculopathy and pseudo‐witelliform dystrophies, OCT‐A helps diagnose choroidal neovascularization. In Progressive cone dystrophies, it could be useful for gaining deeper Knowledge of both the pathogenesis and therapeutic implications.
AbstractList Abstract only
Purpose To assess the ability of swept source optical coherence tomography angiography (SS – OCT‐A) to identify abnormalities of the retinal and choroidal vascular network in macular dystrophies. Methods Optical coherence tomography angiography and structural OCT were performed using a Swept‐source DRI OCT Triton (Topcon, Corporation, Japan) for patients with Stargardt disease, Best maculopathy, pseudo‐vitelliform dystrophy and progressive cone dystrophy. In our series, for every patient the clinical diagnosis was confirmed by the results of molecular genetic study. Results In Stargardt patients, we found alterations especially located at the level of the deep capillary plexus and choriocapillaris. There were different degrees of choriocapillaris impairment, with no residual choriocapillaris inside area of retinal epithelium pigment atrophy in advanced stages. Large choroidal vessels and borders of the atrophy were well visualized. In patients with Best maculopathy and pseudo‐vitelliform dystrophy, OCT‐A revealed neovascularisation in the outer retina and the choriocapillaris while traditional multimodal imaging wasn't conclusive. In progressive cone dystrophy, there was a retinal vasculature signal reduction in both superficial and deep plexus associated with window effect in the outer retina and the choriocapillaris due to the retinal and RPE atrophy. Conclusions In inherited macular distrophies, OCT‐A may provide information of great interest. In stargardt disease, OCT‐A findings were in agreement with the results suggesting primitive severe involvement of choriocapillaris. In Best maculopathy and pseudo‐witelliform dystrophies, OCT‐A helps diagnose choroidal neovascularization. In Progressive cone dystrophies, it could be useful for gaining deeper Knowledge of both the pathogenesis and therapeutic implications.
Purpose To assess the ability of swept source optical coherence tomography angiography (SS - OCT-A) to identify abnormalities of the retinal and choroidal vascular network in macular dystrophies. Methods Optical coherence tomography angiography and structural OCT were performed using a Swept-source DRI OCT Triton (Topcon, Corporation, Japan) for patients with Stargardt disease, Best maculopathy, pseudo-vitelliform dystrophy and progressive cone dystrophy. In our series, for every patient the clinical diagnosis was confirmed by the results of molecular genetic study. Results In Stargardt patients, we found alterations especially located at the level of the deep capillary plexus and choriocapillaris. There were different degrees of choriocapillaris impairment, with no residual choriocapillaris inside area of retinal epithelium pigment atrophy in advanced stages. Large choroidal vessels and borders of the atrophy were well visualized. In patients with Best maculopathy and pseudo-vitelliform dystrophy, OCT-A revealed neovascularisation in the outer retina and the choriocapillaris while traditional multimodal imaging wasn't conclusive. In progressive cone dystrophy, there was a retinal vasculature signal reduction in both superficial and deep plexus associated with window effect in the outer retina and the choriocapillaris due to the retinal and RPE atrophy. Conclusions In inherited macular distrophies, OCT-A may provide information of great interest. In stargardt disease, OCT-A findings were in agreement with the results suggesting primitive severe involvement of choriocapillaris. In Best maculopathy and pseudo-witelliform dystrophies, OCT-A helps diagnose choroidal neovascularization. In Progressive cone dystrophies, it could be useful for gaining deeper Knowledge of both the pathogenesis and therapeutic implications.
Author Maamouri, R.
Chebil, A.
El Matri, K.
El Matri, L.
Falfoul, Y.
Hassairi, A.
Author_xml – sequence: 1
  givenname: L.
  surname: El Matri
  fullname: El Matri, L.
  organization: Institut Hedi Rais of Ophthalmology
– sequence: 2
  givenname: Y.
  surname: Falfoul
  fullname: Falfoul, Y.
  organization: Institut Hedi Rais of Ophthalmology
– sequence: 3
  givenname: K.
  surname: El Matri
  fullname: El Matri, K.
  organization: Institut Hedi Rais of Ophthalmology
– sequence: 4
  givenname: A.
  surname: Hassairi
  fullname: Hassairi, A.
  organization: Institut Hedi Rais of Ophthalmology
– sequence: 5
  givenname: R.
  surname: Maamouri
  fullname: Maamouri, R.
  organization: Institut Hedi Rais of Ophthalmology
– sequence: 6
  givenname: A.
  surname: Chebil
  fullname: Chebil, A.
  organization: Institut Hedi Rais of Ophthalmology
BookMark eNqNkM1Kw0AQxxdRsK2-ggQ8J85-ZJMFL6VYFQo9tIK3Zd1M2oQ2ibstkpvv4Bv6JCZGenYuMwz_33z8x-S8qisk5IZCRLu4KyOaxHHIE5lGDGgSwRwoOyOjU_v8VMevl2TsfQkgqZRiRMLVKvj-_AqWs3Vgqk1Rb5xptm1QVMHe2OPOuCBr_cHVzbZAf0UucrPzeP2XJ-Rl_rCePYWL5ePzbLoILWUpCwUKqiznWSZsklqkb8KalDFQENMYIAaboRJoEbiCLEHZ3Q0ikzkHhbniE3I7zG1c_X5Ef9BlfXRVt1JTxSXjQtKkU8lBZV3tvcNcN67YG9dqCrq3Rpe6_1v3HujeGv1rTQfeD-BHscP2n5SeLlcD_gNZ72jr
ContentType Journal Article
Copyright 2017 The Authors Acta Ophthalmologica © 2017 Acta Ophthalmologica Scandinavica Foundation
Copyright © 2017 Acta Ophthalmologica Scandinavica Foundation
Copyright_xml – notice: 2017 The Authors Acta Ophthalmologica © 2017 Acta Ophthalmologica Scandinavica Foundation
– notice: Copyright © 2017 Acta Ophthalmologica Scandinavica Foundation
DBID AAYXX
CITATION
7TK
DOI 10.1111/j.1755-3768.2017.0F012
DatabaseName CrossRef
Neurosciences Abstracts
DatabaseTitle CrossRef
Neurosciences Abstracts
DatabaseTitleList CrossRef

Neurosciences Abstracts
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1755-3768
EndPage n/a
ExternalDocumentID 10_1111_j_1755_3768_2017_0F012
AOS0F012
Genre abstract
GroupedDBID ---
.3N
.55
.GA
.Y3
05W
0R~
10A
1OB
1OC
23M
31~
33P
36B
3SF
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5HH
5LA
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
AAESR
AAEVG
AAHQN
AAIPD
AAMMB
AAMNL
AANLZ
AAONW
AASGY
AAXRX
AAYCA
AAZKR
ABCUV
ABDBF
ABEML
ABJNI
ABPVW
ABQWH
ABXGK
ACAHQ
ACCZN
ACGFS
ACGOF
ACMXC
ACNCT
ACPOU
ACPRK
ACSCC
ACUHS
ACXBN
ACXQS
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
AEFGJ
AEIGN
AEIMD
AENEX
AEUYR
AEYWJ
AFBPY
AFFPM
AFGKR
AFRAH
AFWVQ
AFZJQ
AGHNM
AGXDD
AGYGG
AHBTC
AHMBA
AIACR
AIDQK
AIDYY
AITYG
AIURR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BAWUL
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BY8
C45
CAG
COF
CS3
D-6
D-7
D-E
D-F
DCZOG
DIK
DPXWK
DR2
DRFUL
DRMAN
DRSTM
E3Z
EAD
EAP
EBC
EBD
EBS
EJD
EMB
EMK
EMOBN
ESX
EX3
F00
F01
F04
F5P
FIJ
FUBAC
G-S
GODZA
H.X
HF~
HGLYW
HZI
HZ~
IX1
J0M
K48
KBYEO
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
O66
O9-
OIG
OVD
P2W
P2X
P2Z
P4B
P4D
P6G
PQQKQ
Q.N
Q11
QB0
R.K
RIWAO
RJQFR
ROL
RX1
SUPJJ
SV3
TEORI
TR2
TUS
UB1
V9Y
W8V
W99
WBKPD
WHWMO
WIH
WIJ
WIK
WIN
WOHZO
WOW
WQJ
WVDHM
WXI
WXSBR
X7M
XG1
~IA
~WT
AAYXX
CITATION
O8X
7TK
ID FETCH-LOGICAL-c1282-4e419c33dd4c78ce1b4ca8220905150050cde94ece0390d7e620104d6f309ef93
IEDL.DBID DRFUL
ISSN 1755-375X
IngestDate Sat Nov 29 15:03:36 EST 2025
Sat Nov 29 01:34:46 EST 2025
Sun Sep 21 06:12:39 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue S259
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c1282-4e419c33dd4c78ce1b4ca8220905150050cde94ece0390d7e620104d6f309ef93
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
PQID 1936234617
PQPubID 1036384
PageCount 1
ParticipantIDs proquest_journals_1936234617
crossref_primary_10_1111_j_1755_3768_2017_0F012
wiley_primary_10_1111_j_1755_3768_2017_0F012_AOS0F012
PublicationCentury 2000
PublicationDate September 2017
2017-09-00
20170901
PublicationDateYYYYMMDD 2017-09-01
PublicationDate_xml – month: 09
  year: 2017
  text: September 2017
PublicationDecade 2010
PublicationPlace Malden
PublicationPlace_xml – name: Malden
PublicationTitle Acta ophthalmologica (Oxford, England)
PublicationYear 2017
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
SSID ssj0061664
Score 2.1542785
Snippet Purpose To assess the ability of swept source optical coherence tomography angiography (SS – OCT‐A) to identify abnormalities of the retinal and choroidal...
Abstract only
Purpose To assess the ability of swept source optical coherence tomography angiography (SS - OCT-A) to identify abnormalities of the retinal and choroidal...
SourceID proquest
crossref
wiley
SourceType Aggregation Database
Index Database
Publisher
SubjectTerms Angiography
Atrophy
Epithelium
Medical imaging
Retina
Tomography
Vascularization
Title SS – OCT angiography in macular dystrophies
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1755-3768.2017.0F012
https://www.proquest.com/docview/1936234617
Volume 95
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVWIB
  databaseName: Wiley Online Library Free Content
  customDbUrl:
  eissn: 1755-3768
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0061664
  issn: 1755-375X
  databaseCode: WIN
  dateStart: 20080101
  isFulltext: true
  titleUrlDefault: https://onlinelibrary.wiley.com
  providerName: Wiley-Blackwell
– providerCode: PRVWIB
  databaseName: Wiley Online Library Full Collection 2020
  customDbUrl:
  eissn: 1755-3768
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0061664
  issn: 1755-375X
  databaseCode: DRFUL
  dateStart: 20080101
  isFulltext: true
  titleUrlDefault: https://onlinelibrary.wiley.com
  providerName: Wiley-Blackwell
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3PT8IwFH5BMMaLv40okh28TsfWruuRoAsmCEYgclu6tlMODgJo4s3_wf_Qv8S22xTixRhvzZI2y5f3-r62730P4Iz6SFKBuW6TSmzkx8yOCQ9sj0nCPZcKjk2hcId0u8FoRG9L0C5qYTJ9iK8LN-0ZZr_WDs7i-aqTE4y1g5gMLXLuhI5uN1xxlRHjMlQu78Jhp9iV_YZvpKTyOXiUVwsXWT0_V1oNVN_sc5nDmiAUbv_f7-_AVk5ErWZmObtQkukebNzkT-37YPf71sfbu9VrDSyWPoxzaWtrnFpPzCSvWuJ1vphNpo_qsH0Aw_Bq0GrbeW8Fm6uI5NpIogblnicE4iTgshEjzhRZcLReF9aqMFxIiqRuJ0YdQaSvn82R8BPPoTKh3iGU00kqj8ASGMWBL1jSYDHyPMwSh7qBiv2KujFBUBUuCiCjaSahES0dPRQKkUYh0ihEBoUq1Aq8o9yl5pFimoqqIcW4qoANsr9cLWr2-mZw_Md5J7Cpv2aZZTUoL2bP8hTW-ctiPJ_Vc0Orw9r9dfcT8lzO4Q
linkProvider Wiley-Blackwell
linkToHtml http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1NTwMhECWmGvXit7FalYPX1W2BZTk2jU0b261Ja-yNsMBqD26btpp48z_4D_0lArurbbwY440DEPLCMA-YeQPABQuwZopIWyaVejiIhRdTGXpIaCpRjSlJXKJwh0ZROByy21xSyObCZPoQXw9u1jLceW0N3D5IL1s5JcRaiAvRopd-07f1hlexYR22isN9OyoO5aAaOCWpfAQZ5snCRVDPz3mW_dQ3-VyksM4HNbf_cfU7YCsnorCe7ZxdsKLTPbDezb_a94HX78OPt3fYawygSB9GubQ1HKXwSbjgVaheZ_PpePJoLtsH4K55PWi0vLy2gieNR6p5WOMqkwgphSUNpa7GWApDFnyr10WsKoxUmmFty4kxX1Ed2G9zrIIE-UwnDB2CUjpO9RGAiuA4DJRIqiLGCBGR-KwWGt9vqJtQFJfBVYEkn2QSGnzh6mFQ4BYFblHgDoUyqBSA89ykZtwwTUPVsGFcZUActL-cjdd7fdc4_uO4c7DRGnQ7vNOObk7Apu2RRZlVQGk-fdanYE2-zEez6Znbc58pFtCU
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=SS+%E2%80%93+OCT+angiography+in+macular+dystrophies&rft.jtitle=Acta+ophthalmologica+%28Oxford%2C+England%29&rft.au=El+Matri%2C+L.&rft.au=Falfoul%2C+Y.&rft.au=El+Matri%2C+K.&rft.au=Hassairi%2C+A.&rft.date=2017-09-01&rft.issn=1755-375X&rft.eissn=1755-3768&rft.volume=95&rft.epage=n%2Fa&rft_id=info:doi/10.1111%2Fj.1755-3768.2017.0F012&rft.externalDBID=10.1111%252Fj.1755-3768.2017.0F012&rft.externalDocID=AOS0F012
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1755-375X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1755-375X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1755-375X&client=summon