[Downloaded free from http://www.ijo.in on Sunday, April 22, 2018, IP: 151.252.66.202]
419
Brief Communications September - October 2010
In our study, we found that both age and type of refractive error do not have any statistically significant association with the DFA. The variation in DFA could be due to biological variability.
Conclusion We have established the physiological range of DFA in children in the Indian population. The minimal intraindividual variation (inter-eye variation) in children (not cooperative for the subjective tests) may help regarding their torsional status. Since the inter-eye variability is small, if the inter-eye DFA variability is large in a child, the child could have a torsional disturbance and should be evaluated for the same.
References 1. Herzau V, Joos-Kratsch E. Objective and subjective evaluation of cyclovergence and cyclofusion. Doc Ophthalmol 1984;58:85-90. 2. Madigan WP Jr, Katz NN. Ocular torsion-direct measurement with indirect ophthalmoscope and protractor. J Pediatr Ophthalmol
A case of central retinal artery occlusion following embolization procedure for juvenile nasopharyngeal angiofibroma Alireza Ramezani, Hamidreza Haghighatkhah , Habibollah Moghadasi2, Morteza Sanei Taheri1, Hiva Parsafar
Strabismus 1992;29:171-4. 3. Lefèvre F, Leroy K, Delrieu B, Lassale D, Péchereau A. Study of the optic nerve head-fovea angle with retinophotography in healthy patients. J Fr Ophtalmol 2007;30:598-606. 4. Kothari MT, Venkatesan G, Shah JP, Kothari K, Nirmalan PK. Can ocular torsion be measured using the slitlamp biomicroscope? Indian J Ophthalmol 2005;53:43-7. 5. de Ancos E, Klainguti G. An objective measure of ocular torsion: A new indirect ophthalmoscopy lens. Klin Monatsbl Augenheilkd 1994;204:360-2. 6. Rohrschneider K. Determination of the location of the fovea on the fundus. Invest Ophthalmol Vis Sci 2004;45:3257-8. 7. Williams TD, Wilkinson JM. Position of the fovea centralis with respect to the optic nerve head. Optom Vis Sci 1992;69:369-77. 8. Bixenman WW, Noorden GK Von. Apparent foveal displacement in normal subjects and in cyclotropia. Ophthalmology 1982;89:58-61. 9. Keilhauer C, Zollmann J, Schrader W, Delori F. Verlagert sich mit zunehmendem Alter die Fovea relativ zur Papille? Ophthalmologe 2003;100:S164.
Key words: Central retinal artery occlusion, embolization, juvenile nasopharyngeal angiofibroma Indian J Ophthalmol: 2010;58:419-421
DOI: 10.4103/0301-4738.67065
PMID: ***
1
A 23-year-old male patient with right nasal Juvenile Nasopharyngeal Angiofibroma (JNA) developed Central Retinal Artery Occlusion (CRAO) during embolization of the tumor using polyvinyl alcohol particles before endoscopic excision. Classic CRAO management was initiated by an ophthalmologist after 12 h. Retrospective evaluation of the angiograms revealed a tiny communication between the external carotid and ophthalmic arteries which had not been noticed before embolization. During endoscopic excision, the tumor was found to originate extraordinarily from midline structures. It was concluded that CRAO might be a rare complication of JNA embolization. Careful preoperative angiographic evaluations to detect communicating arteries and immediate ophthalmologic consultation in case of developing visual symptoms during the procedure are necessary.
Department of Ophthalmology, Imam Hossein Medical Center, 1 Department of Radiology, Shohada-e-tajrish Medical Center, 2 Department of Otolaryngology, Loghman-e-hakim Medical Center, Shaheed Beheshti Medical University, Tehran, Iran Correspondence to: Dr. Alireza Ramezani, Ophthalmic Research Center of Shahid Beheshti Medical University (M.C), Labbafinejad Medical Center, Pasdaran Ave. Boostan 9 St. Tehran-166 66, Iran. E-mail:
[email protected] Manuscript received: 16.01.09; Revision accepted: 11.06.09
Central Retinal Artery Occlusion (CRAO) is one of the most sudden and dramatic events seen by ophthalmologists. One of the major causes of CRAO is embolism. There are many procedures associated with embolic complications and interventional radiological procedures are among the rare ones.[1] Juvenile Nasopharyngeal Angiofibroma (JNA), one of the common benign nasal cavity tumors of adolescence, exhibits a strong tendency to bleed during surgical removal. Nowadays, preoperative embolization is commonly used to minimize such intraoperative bleeding; however, this technique is not without complications.[2,3] Here, we present a rare case of CRAO which occurred following preoperative embolization in a patient with JNA. It also provides an opportunity to discuss two pitfalls which occurred during the patient’s management.
Case Report A 23-year-old male patient presented with the complaint of right nasal obstruction. After observing a purple pink mass completely filling the right nasal cavity, the diagnosis of JNA was made. Computerized tomography revealed a nasal cavity mass extending partially to the sphenoid sinus, pterygomaxillary fossa, and infratemporal fossa. In order to reduce bleeding during the later endoscopic resection, the patient underwent a transarterial particulate embolization procedure as a part of preoperative preparation. After catheterization of both external carotid arteries with
[Downloaded free from http://www.ijo.in on Sunday, April 22, 2018, IP: 151.252.66.202]
420
Indian Journal of Ophthalmology
5 F MP catheters (Cordis) via right transfemoral approach, selective angiography was performed. Abnormal tumor blush [Fig. 1, arrowhead] was noted with bilateral supply from both internal maxillary and ascending pharyngeal arteries. Neither extracranial-intracranial communication nor external-internal carotid collateral artery was detected. Therefore, embolization process was carried out bilaterally using Polyvinyl Alcohol (PVA) particles (150-250 micrometer) through both internal maxillary and ascending pharyngeal arteries. The progress of the vascular occlusion during embolization was monitored with repeated hand injection of contrast media. Before finishing the embolization the patient complained of sudden loss of vision in his left eye. After a control angiography, the procedure was stopped and 5000 IU heparin was injected intravenously. Immediate post-embolization angiograms demonstrated a successful reduction of the tumor blush with no reperfusion. After 12 h, the patient was examined by an ophthalmologist in another hospital. Left eye visual acuity (VA) was counting finger at 0.5 meter and the relative afferent pupillary defect was positive in this eye. Left fundus examination revealed retinal edema and a ‘‘cherry-red spot’’ appearance of the macula with narrowed vessels, which were compatible with the diagnosis of CRAO. Ocular massage, anterior chamber paracentesis as well as systemic therapy with carbonic anhydrase inhibitor and mannitol were initiated. During the follow-up, VA stabilized at 20/200. Retrospective and precise reevaluation of pre-embolization angiograms revealed a suspicious tiny communication between the external carotid artery and ophthalmic vessels on the left side [Fig. 1, arrow]. Such a communication was not found on the right side. Four months after the embolization process, the patient underwent a successful endoscopic angiofibroma en bloc excision. Interestingly, the tumor was found to originate from midline structures and attached to the posterior free border of the nasal septum. Fourteen months after embolization, VA was 20/200. Cherryred spot disappeared leaving attenuated retinal arterioles and optic disc atrophy.
Vol. 58 No. 5
Discussion Many CRAOs are embolic in origin. Radiologic procedures including hysterosalpingography, arteriography, cardiac catheterization, and interventional procedures are among the many different conditions that can cause embolus formation.[1] Preoperative embolization in the treatment of various tumors may be a cause of such emboli formation and subsequent organ infarction. CRAO as a complication of embolization in the management of JNA has rarely been reported previously.[4,5] It has been known that inadvertent embolization of the brain or eye during JNA management occurred via dangerous collaterals from the internal maxillary artery to the intracranial/ intraorbital contents. Önerci et al. presented a patient with JNA who developed CRAO following preoperative embolization. They could not demonstrate any responsible communicating artery and therefore assumed the existence of a branch of the internal maxillary artery supplying the intraorbital contents and the retina in their case. Hence, they recommended more detailed assessment of these possible dangerous collaterals by superselective catheterization of the internal maxillary artery branches with microcatheters.[4] In our case, however, careful retrospective review of the angiograms revealed the presence of a suspicious collateral artery between the external carotid artery and ophthalmic vessels on the left side which had not been noticed before embolization. Thus, it is more probable that the embolus passed mostly via this collateral artery to the left central retinal artery while tumor embolization was being carried out through the left side arteries. The other pitfall encountered in our case was the delay in the management of CRAO. It was mostly due to the lack of an ophthalmologist in the primary center in which radiologic intervention was performed. To make this presentation concise we will not elaborate on the management of CRAO. However, since the precious time for keeping the retinal cells alive by restoring the retinal artery flow is estimated to be about 90 min,[6] this report underlines the importance and benefits of radiologists’ familiarity with the early diagnosis and immediate therapies of CRAO. Nonetheless, the current recommended treatments may not be more effective than the natural course of the disease.[7,8] During surgical removal of the tumor, it was noted that the tumor had an extraordinary origin from the midline as opposed to the usual lateral location of the tumor pedicle in the majority of JNA cases. The association of this rare tumor position with the existence of a collateral vessel in our case might have happened by chance and we could not reach any conclusion in this regard. This case report introduces a patient with CRAO as a rare but an important complication following preoperative embolization of an unusually located JNA tumor. This case also highlights the necessity of careful evaluation of angiograms for detection of any abnormal collateral vessel(s) prior to embolization and the importance of immediate diagnosis and treatment in patients who develop ocular symptoms during or shortly after the interventional procedures.
Figure 1: Pre-embolization angiogram demonstrating tumor bush (arrow head) and a suspicious tiny communicating artery between external carotid and ophthalmic arteries (arrows)
References 1. Sanborn GE, Magargal LE. Arterial obstructive disease of the eye. In: Duane’s clinical ophthalmology [book on CD-ROM].
[Downloaded free from http://www.ijo.in on Sunday, April 22, 2018, IP: 151.252.66.202] Brief Communications September - October 2010 Vol. 3, Chap. 14. Philadelphia: Lippincott Williams and Wilkins Publishers; 2006. 2. Douglas R, Wormald PJ. Endoscopic surgery for juvenile nasopharyngeal angiofibroma: Where are the limits? Curr Opin Otolaryngol Head Neck Surg 2006;14:1-5.
421
5. Lloyd G, Howard D, Phelps P, Cheesman A. Juvenile angiofibroma: The lessons of 20 years of modern imaging. J Laryngol Otol 1999;113:127-34. 6. Hayreh SS, Kolder HE, Weingeist TA. Central retinal artery occlusion and retinal tolerance time. Ophthalmology 1980;87:75-8.
3. Onerci M, Gumus K, Cil B, Eldem B. A rare complication of embolization in juvenile nasopharyngeal angiofibroma. Int J Pediatr Otorhinolaryngol 2005;69:423-8.
7. Atebara NH, Brown GC, Cater J. Efficacy of anterior chamber paracentesis and Carbogen in treating acute nonarteritic central retinal artery occlusion. Ophthalmology 1995;102:2029-34.
4. Casasco A, Houdart E, Biondi A, Jhaveri HS, Herbreteau D, Aymard A, et al. Major complications of percutaneous embolization of skullbase tumors. AJNR Am J Neuroradiol 1999;20:179-81.
8. Brown Gc. Arterial occlusive disease. In: Regillo CD, Brown GC, Flynn HW Jr, editors. Vitreoretinal Disease: The Essentials. New York: Thieme; 1999. p. 97-115.
In vivo growth of retinoblastoma in a newborn infant
Case Report
Parag K Shah, V Narendran, N Kalpana Retinoblastoma is a rare malignancy of the retina seen exclusively in children. It is known to cause rapid growth inside the eye and hence treatment should be started as soon as it is diagnosed. We report a case in a five-day-old infant in whom treatment (chemotherapy) was delayed by a month due to high bilirubin levels secondary to physiological jaundice, which gave us the unique opportunity to measure the growth of the tumor over a month. This case emphasizes that immediate treatment is warranted once this rare disease is diagnosed. Key words: Half-dose carboplatin, growth measure, in vivo, retinoblastoma Indian J Ophthalmol: 2010;58:421-423
DOI: 10.4103/0301-4738.67066
PMID: ***
Retinoblastoma is the commonest intraocular malignancy of childhood.[1] It has been shown to grow rapidly in the eye.[2] Uncontrolled growth can lead to not only destruction of the eye but also extraocular metastasis. There has been only one report[2] where they have measured the growth of the tumor over 13 days in a preterm newborn who was diagnosed to have retinoblastoma and was waiting for brachytherapy. We report a case of a full-term newborn with bilateral disease, where we had the opportunity to observe the growth of the tumor in one eye over 35 days, while the child was waiting for the physiological jaundice to come down in order to start full-dose systemic chemotherapy.
Pediatric Retina and Ocular Oncology Department, Aravind Eye Hospital & Postgraduate Institute of Ophthalmology, Coimbatore, Tamil Nadu, India Correspondence to: Dr. Parag K. Shah, Department of Pediatric Retina and Ocular Oncology, Aravind Eye Hospital, Avinashi Road, Coimbatore641 014, Tamil Nadu, India. E-mail:
[email protected] Manuscript received: 20.02.09; Revision accepted: 13.04.09
A five-day-old newborn, with a positive family history of retinoblastoma was referred to our institute with a possibility of the same in left eye (LE). On fundus examination right eye (RE) showed three small tumors (< 1 mm in size), two above the supero-temporal arcade vessels and one nasal to the disc. LE showed a solid elevated mass over the macula. The horizontal diameter of that mass was 5.8 mm; vertical diameter was 5.6 mm while the height on B scan was 3.1 mm [Figs. 1a and 1b]. The area of the tumor base was 24.5 mm2 and it was 0.24 mm from the temporal margin of the optic disc. A smaller mass with horizontal diameter of 1.7 mm and vertical diameter of 1.5 mm was also present touching the main mass in the supero-temporal quadrant. Transpupillary thermotherapy (TTT) was applied to all the three tumors in RE while systemic chemotherapy was decided for the LE. Unfortunately, on referring to our oncologist, the child was found to have physiological jaundice with the bilirubin levels at 22 mg/dl. The child was subjected to phototherapy and chemotherapy was deferred by two weeks. On Day 16 the bilirubin levels were still high at 5.7 mg/dl and the tumor size in LE had increased. Now, the horizontal diameter was 7.2 mm, vertical was 6.8 mm, height was 3.5 mm [Figs. 2a and 2b] and basal area was 39.8 mm2. The tumor was now touching the temporal disc margin. The smaller mass was almost fused with the main tumor. Another small tumor (< 1 mm in diameter) was seen nasal to disc for which TTT was done. Brachytherapy was deferred as there was more than one mass and it would take two to three weeks for the iodine 125 (I 125) seeds to be prepared. Moreover our brachytherapy experience was limited, especially in newborns. To start some form of treatment immediately, we decided to give half-dose carboplatin. The normal dose is 18.6 mg/kg. We administered 9.3 mg/kg. The tumors in the RE were scarred. Two weeks after the half-dose carboplatin (Day 35 from initial diagnosis) was started the horizontal diameter had increased to 8.7 mm, vertical to 7.8 mm, height to 5.6 mm [Figs. 3a and 3b] and basal area to 55.7 mm2. The tumor was now overlapping the temporal disc margin. The nasal tumor had scarred post TTT laser. Fortunately, at that point the bilirubin levels had become normal and full-dose three-drug chemotherapy (carboplatin, etoposide, vincristine) was started immediately. The tumor responded well and after completing six cycles of chemotherapy, at six-month follow-up, it had regressed into a calcified mass (Type 1 regression). This delay in starting the treatment gave us the unique opportunity to study the growth of the tumor over a month in vivo.
