|A case of incomplete central retinal artery occlusion associated with short posterior ciliary artery occlusion.|
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|PMID: 23365775 Owner: NLM Status: PubMed-not-MEDLINE|
|To our knowledge, incomplete central retinal artery occlusion associated with short posterior ciliary artery occlusion is extremely rare. Herein, we describe a case of a 62-year-old man who was referred to our hospital with of transient blindness in his right eye. At initial examination, the patient's best-corrected visual acuity was 18/20 in the right eye. Fundus examination showed multiple soft exudates around the optic disc and mild macular retinal edema in his right eye; however, a cherry red spot on the macula was not detected. Fluorescein angiography revealed delayed dye inflow into the nasal choroidal hemisphere that is supplied by the short posterior ciliary artery. The following day, the patient's visual acuity improved to 20/20. Soft exudates around the optic disc increased during observation and gradually disappeared. His hemodynamic parameters revealed subclavian steal syndrome as examined by cervical ultrasonography and digital subtraction angiography. We speculate that his transient blindness was due to ophthalmic artery spasms. In this particular case, spasms of the ophthalmic artery and occlusion of the short posterior ciliary artery occurred simultaneously. As the short posterior ciliary artery branches from the ophthalmic artery, the anatomical location of the lesion might be near the branching of both arteries.|
|Shinji Makino; Mikiko Takezawa; Yukihiro Sato|
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|Type: Journal Article Date: 2013-01-13|
|Title: Case reports in ophthalmological medicine Volume: 2013 ISSN: 2090-6722 ISO Abbreviation: Case Rep Ophthalmol Med Publication Date: 2013|
|Created Date: 2013-01-31 Completed Date: 2013-02-01 Revised Date: 2013-04-18|
Medline Journal Info:
|Nlm Unique ID: 101581018 Medline TA: Case Rep Ophthalmol Med Country: United States|
|Languages: eng Pagination: 105653 Citation Subset: -|
|Department of Ophthalmology, Jichi Medical University, 3311-1 Yakushiji, Tochigi, Shimotsuke 329-0498, Japan.|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Case Rep Ophthalmol Med
Journal ID (iso-abbrev): Case Rep Ophthalmol Med
Journal ID (publisher-id): CRIM.OPHMED
Publisher: Hindawi Publishing Corporation
Copyright © 2013 Shinji Makino et al.
Received Day: 12 Month: 12 Year: 2012
Accepted Day: 1 Month: 1 Year: 2013
Print publication date: Year: 2013
Electronic publication date: Day: 13 Month: 1 Year: 2013
Volume: 2013E-location ID: 105653
PubMed Id: 23365775
|A Case of Incomplete Central Retinal Artery Occlusion Associated with Short Posterior Ciliary Artery Occlusion|
|Department of Ophthalmology, Jichi Medical University, 3311-1 Yakushiji, Tochigi, Shimotsuke 329-0498, Japan
|Correspondence: *Shinji Makino: firstname.lastname@example.org
[other] Academic Editors: S. Machida, M. B. Parodi, and P. Venkatesh
There are only few reports in the Japanese literature that have presented the incomplete type of central retinal artery occlusion (CRAO), including diminished visual acuity and a residual visual field but no complete visual loss, slight retinal edema together with a slight cherry red spot on the macula, and good visual prognosis [1, 2].
The ophthalmic artery enters the orbit through the optic canal, usually inferotemporal to the optic nerve. The vessel soon crosses medially over the nerve and gives rise to its first branch, the central retinal artery. After the central retinal artery branches from the ophthalmic artery, a varying number of posterior ciliary arteries arise. Each of these major posterior ciliary arteries further divides into multiple short posterior ciliary branches that penetrate the sclera medial or lateral to the optic nerve, depending on their respective deviation from the parent medial or lateral posterior ciliary arteries [3–5].
There have been several reports presenting CRAO with choroidal circulatory disturbance [6–8], and/or anterior ischemic optic neuropathy [7, 9–11]. To our knowledge, incomplete CRAO associated with short posterior ciliary artery occlusion is extremely rare . Herein, we describe the case of such a patient.
A 62-year-old man complaining of transient blindness in his right eye on waking was referred to our hospital. The patient had a history of hypertension and hyperlipidemia. At initial examination, he had a best-corrected visual acuity of 18/20 in the right eye, which was noncorrigent, and 20/20 in the left eye. Ocular pressures were normal. Slit lamp examination showed cortical opacities in both lenses. Fundus examination showed multiple soft exudates around the optic disc and mild retinal edema in the macula of his right eye; however, a cherry red spot was not detected, and the optic disc appearance was unremarkable (Figure 1). Fluorescein angiography (FA) revealed a delay of arm-to-retina time and a marked filling delay of the nasal choroidal hemisphere that is supplied by nasal short posterior ciliary artery (Figure 2(a)). Therefore, the choriocapillaris corresponding to the nasal choroidal area filled slowly and patchily (Figure 2(b)), and no staining of the arterial wall was detected in the late stage. From these findings, the patient was diagnosed with incomplete CRAO associated with short posterior ciliary artery occlusion. Systemic administration of a vasodilator and an antiplatelet agent were started after the initial examination. On the following day, his right visual acuity improved to 20/20. However, during observation, soft exudates increased 2 days after the initial visit (Figure 3(a)), increased further at 1 week (Figure 3(b)), gradually decreased in 2 weeks (Figure 3(c)), and finally disappeared at 7 weeks (Figure 3(d)). The patient's blood pressure was 95/80 mmHg in the right arm and 130/80 mmHg in the left arm. Further examinations for evaluating hemodynamics were performed; cervical ultrasonography revealed right subclavian artery stenosis and reversed right vertebral artery flow. Additionally, digital subtraction angiography demonstrated the stenosis of the following arteries: from the right common carotid artery to the bifurcation of the internal carotid artery, the right brachiocephalic trunk, the right subclavian artery, and the left common carotid artery. On the basis of these findings, he was also diagnosed with subclavian steal syndrome. After recovery from this event, he did not experience any additional periods of transient blindness.
In 2002, Schmidt et al.  classified CRAO into 3 stages; stage I of his classification represents “incomplete CRAO” and includes diminished visual acuity and a residual visual field but no complete visual loss, slight retinal edema together with a slight cherry red spot on the macula, no increase in retinal signs over several hours, and delayed but not completely interrupted blood flow revealed by FA. They also reported that spontaneous recovery usually did not occur during a followup of several hours despite minor retinal findings. The fundus changes in stage I described in their literature  were very similar to those in our case.
Hagimura et al.  evaluated 22 patients with CRAO. Eyes with poor final vision (final visual acuity < 0.1, n = 14) showed initially denser retinal opacities with a distinct cherry red spot. Eyes with favorable visual outcome (final visual acuity > 0.4, n = 7) showed soft exudates and faint retinal opacities without a cherry red spot. The findings show that the final visual outcome mainly depended on the initial visual acuity and funduscopic findings. In our patient, soft exudates were defined during observation and the patient's final visual acuity was 20/20.
There have been few reports in the Japanese literature presenting incomplete CRAO, including diminished visual acuity and a residual visual field but no complete visual loss, slight retinal edema together with a slight cherry red spot on the macula, and good visual prognosis [1, 2]. The fundus changes seen in these reported cases [1, 2] were very similar to those seen in our case. There have been several reports of CRAO presenting with choroidal circulatory disturbance [6–8], and/or anterior ischemic optic neuropathy [7, 9–11]. To our knowledge, incomplete CRAO associated with short posterior ciliary artery occlusion is extremely rare .
Our patient also had subclavian steal syndrome. Subclavian steal syndrome is a function of the proximal subclavian artery stenoocclusive disease with subsequent retrograde blood flow in the ipsilateral vertebral artery . Morita et al.  described subclavian steal syndrome in a case of arteritis syndrome with bilateral occlusion of common carotid arteries. Souma et al.  described a case of reversed ophthalmic artery flow without occlusion of the internal carotid artery. Although, in their patient, collateral circulation and reversed ophthalmic artery flow were not blurred, stenosis of common carotid and internal carotid arteries were detected. Therefore, it is apparent that our patient had circulation disturbances in the right internal carotid artery and the right ophthalmic artery.
In conclusion, we speculate that the transient blindness experienced by our patient was due to spasms of the ophthalmic artery. In this case, spasms of the ophthalmic artery and occlusion of the short posterior ciliary artery occurred simultaneously. As the short posterior ciliary artery branches from the ophthalmic artery, the anatomical location of the lesion is likely located near the branching of both arteries.
The authors have no financial or proprietary interests related to this paper.
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