Structural Abnormalities of the Inner Macula in Incontinentia Pigmenti

被引:22
作者
Basilius, Jacob [1 ]
Young, Marielle P. [2 ]
Michaelis, Timothy C. [1 ]
Hobbs, Ronald [2 ]
Jenkins, Glen [2 ]
Hartnett, M. Elizabeth [2 ]
机构
[1] Univ Utah, Sch Med, Salt Lake City, UT USA
[2] Univ Utah, Dept Ophthalmol & Visual Sci, John A Moran Eye Ctr, Salt Lake City, UT 84132 USA
关键词
BLOCH-SULZBERGER SYNDROME; OF-THE-LITERATURE; MANIFESTATIONS; SERIES;
D O I
10.1001/jamaophthalmol.2015.1700
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
IMPORTANCE This report presents evidence from spectral-domain optical coherence tomography and fluorescein angiography of inner foveal structural abnormalities associated with vision loss in incontinentia pigmenti (IP). OBSERVATIONS Two children had reduced visual behavior in association with abnormalities of the inner foveal layers on spectral-domain optical coherence tomography. Fluorescein angiography showed filling defects in retinal and choroidal circulations and irregularities of the foveal avascular zones. The foveal to parafoveal ratios were greater than 0.57 in 6 eyes of 3 patients who had extraretinal neovascularization and/or peripheral avascular retina on fluorescein angiography and were treated with laser. Of these, 3 eyes of 2 patients had irregularities in foveal avascular zones and poor vision. CONCLUSIONS AND RELEVANCE Besides traction retinal detachment, vision loss in IP can occur with abnormalities of the inner foveal structure seen on spectral-domain optical coherence tomography, consistent with prior descriptions of foveal hypoplasia. The evolution of abnormalities in the neural and vascular retina suggests a vascular cause of the foveal structural changes. More study is needed to determine any potential benefit of the foveal to parafoveal ratio in children with IP. Even with marked foveal structural abnormalities, vision can be preserved in some patients with IP with vigilant surveillance in the early years of life.
引用
收藏
页码:1067 / 1072
页数:6
相关论文
共 15 条
[1]   Incontinentia pigmenti in boys: A series and review of the literature [J].
Ardelean, Daniela ;
Pope, Elena .
PEDIATRIC DERMATOLOGY, 2006, 23 (06) :523-527
[2]   Incontinentia pigmenti: A review and update on the molecular basis of pathophysiology [J].
Berlin, AL ;
Paller, AS ;
Chan, LS .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2002, 47 (02) :169-187
[3]   INCONTINENTIA PIGMENTI [J].
CARNEY, RG .
ARCHIVES OF DERMATOLOGY, 1976, 112 (04) :535-542
[4]   Insight into IKBKG/NEMO Locus: Report of New Mutations and Complex Genomic Rearrangements Leading to Incontinentia Pigmenti Disease [J].
Conte, Matilde Immacolata ;
Pescatore, Alessandra ;
Paciolla, Mariateresa ;
Esposito, Elio ;
Miano, Maria Giuseppina ;
Lioi, Maria Brigida ;
McAleer, Maeve A. ;
Giardino, Giuliana ;
Pignata, Claudio ;
Irvine, Alan D. ;
Scheuerle, Angela E. ;
Royer, Ghislaine ;
Hadj-Rabia, Smail ;
Bodemer, Christine ;
Bonnefont, Jean-Paul ;
Munnich, Arnold ;
Smahi, Asma ;
Steffann, Julie ;
Fusco, Francesca ;
Ursini, Matilde Valeria .
HUMAN MUTATION, 2014, 35 (02) :165-177
[5]   Incontinentia pigmenti [J].
Francis, JS ;
Sybert, VP .
SEMINARS IN CUTANEOUS MEDICINE AND SURGERY, 1997, 16 (01) :54-60
[6]  
GOLDBERG MF, 1993, OPHTHALMOLOGY, V100, P1645
[7]   The skin is not the predominant problem in incontinentia pigmenti [J].
Goldberg, MF .
ARCHIVES OF DERMATOLOGY, 2004, 140 (06) :748-750
[8]   THE BLINDING MECHANISMS OF INCONTINENTIA PIGMENTI [J].
GOLDBERG, MF .
OPHTHALMIC GENETICS, 1994, 15 (02) :69-76
[9]   Ocular manifestations of incontinentia pigmenti [J].
Holmström, G ;
Thorén, K .
ACTA OPHTHALMOLOGICA SCANDINAVICA, 2000, 78 (03) :348-353
[10]   SECTORAL RETINAL NERVE FIBER LAYER THINNING IN BRANCH RETINAL VEIN OCCLUSION [J].
Kim, Chang-Sik ;
Shin, Kyung-Sup ;
Lee, Haeng-Jin ;
Jo, Young-Joon ;
Kim, Jung-Yeul .
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2014, 34 (03) :525-530