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  Most popular articles (Since October 30, 2020)

 
 
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EDITIORIAL
A picture is worth a thousand words
Santosh G Honavar
April-June 2021, 1(2):159-159
DOI:10.4103/ijo.IJO_723_21  
  879 156 -
OPHTHALMIC IMAGES
Ota with Ito: An unusual concurrence
Muthukrishnan Vallinayagam, Juhi Sahu, Anujeet Paul, Krishnagopal Srikanth
January-March 2021, 1(1):13-13
DOI:10.4103/ijo.IJO_2081_20  
  978 54 -
CASE REPORTS
Unveiling a rare aetiology of secondary acquired nasolacrimal duct obstruction: A case of morning glory syndrome with contralateral naso-ethmoidal encephalocele
Muthukrishnan Vallinayagam, Shravya C Balla, Anujeet Paul, Srikanth Krishnagopal
April-June 2021, 1(2):373-375
DOI:10.4103/ijo.IJO_2378_20  
Morning Glory Syndrome (MGS) is a well-established association of basal encephalocele and usually presents with midline cranio-facial anomalies. 45-year-old female presented with Secondary Acquired Nasolacrimal Duct Obstruction (SANDO) in left eye. She had a broad nasal bridge, hypertelorism and a swelling inferomedial to medial canthus. Fundus examination in right eye showed Morning Glory disc anomaly. CT of the orbit and brain disclosed left naso-ethmoidal encephalocele. CT Dacryocystography showed partial dehiscence of nasolacrimal duct bilaterally. The patient underwent surgical repair of encephalocele followed by resolution of epiphora. The association of MGS with contralateral naso-ethmoidal encephalocele and SANDO is presented for its rarity.
  900 12 -
EDITIORIAL
The story is the thing - The birth of Indian Journal of Ophthalmology Case Reports
Santosh G Honavar
January-March 2021, 1(1):1-1
DOI:10.4103/ijo.IJO_3810_20  
  796 115 -
OPHTHALMIC IMAGES
Verrucous carcinoma: A rare variant of eyelid squamous cell carcinoma
Tarjani V Dave, Sasi Pyda
January-March 2021, 1(1):4-4
DOI:10.4103/ijo.IJO_1600_20  
  690 87 -
CASE REPORTS
Nevus of Ota with palatal involvement and Helicobacter pylori gastritis: A rare case report
Dipankar Das, Prafulla Sarma, Kamal Chetri, Harsha Bhattacharjee, Saurabh Deshmukh, Nitu Kumari, Kunal Shinde
January-March 2021, 1(1):83-84
DOI:10.4103/ijo.IJO_585_20  
Congenital oculodermal melanocytosis is also known as Nevus of Ota, condition where blue nevus of skin and orbit are seen with ipsilateral nevus in conjunctiva and iris. They are often associated with glaucoma which can occur at any age. They can have melanocytosis and develop choroidal melanoma. We report a case of a middle-aged female with facial pigmentation and bilateral scleral, conjunctival, and iris nevus with an advanced glaucomatous change in both eyes and pigmentation of the palatal mucosa. Trabeculectomy with mitomycin-C application was done in the left eye. Gastrointestinal endoscopy by gastroenterologist showed gastritis and Helicobacter pylori infection.
  721 31 -
OPHTHALMIC IMAGES
Goblet cell anatomy visualization by scanning electron microscopy
Carlos Rocha de Lossada, Rahul Rachwani Anil, Javier Lacorzana Rodríguez, Davide Borroni, Jorge Peraza-Nieves
April-June 2021, 1(2):161-161
DOI:10.4103/ijo.IJO_2507_20  
  594 109 -
Feathery cataract
Syed Mohideen Abdul Khadar, Smital M Metange
April-June 2021, 1(2):162-162
DOI:10.4103/ijo.IJO_3388_20  
  546 122 -
CASE REPORTS
Rubella eye disease: A clinicopathological case report
Dipankar Das, Jayanta Kumar Das, Balmukund Agarwal, Harsha Bhattacharjee, Gayatri Bharali, Debajit Deka, Deb Kumar Mahato, Saurabh Deshmukh, Apurba Deka
April-June 2021, 1(2):317-319
DOI:10.4103/ijo.IJO_2621_20  
Rubella is a viral disease that affects human particularly pregnant females and causes transplacental spread to affect the fetus in utero. Congenital rubella in a child can manifest from mild to severe involvement. We report a case of a young boy with bilateral blindness and sensorineural deafness. Enucleated eye revealed the evidence of rubella eye disease. TORCH titer showed increase of IgG antibody in the serum. An extensive systemic examination and investigations by physician did not show any other signs of extended rubella syndrome.
  618 23 -
OPHTHALMIC IMAGES
Periocular cutaneous leishmaniasis
Md Shahid Alam, Sanhita Chatterjee
January-March 2021, 1(1):5-5
DOI:10.4103/ijo.IJO_1766_20  
  555 71 -
CASE REPORTS
Active concurrent central serous chorioretinopathy and pachychoroid neovasculopathy managed with combination therapy of photodynamic therapy and anti-vascular endothelial growth factor agent
Barun Garg, Isha Gupta, Sugandha Goel, Deepak Senger, Kumar Saurabh, Rupak Roy
January-March 2021, 1(1):123-126
DOI:10.4103/ijo.IJO_836_20  
Pachychoroid disease spectrum includes central serous chorioretinopathy (CSR) and pachychoroid neovasculopathy (PNV). Pachychoroid phenotype is characterized by choroidal hyperpermeability, dilated choroidal vessels (pachyvessels), and focal or diffuse increase in choroidal thickness. Newer imaging modalities have aided in the diagnosis of choroidal diseases. Herein, we present a case of active concurrent CSR with PNV in a middle-aged patient with successful treatment by photodynamic therapy and intravitreal anti-vascular endothelial growth factor (VEGF) (ranibizumab) injection.
  526 31 -
GUEST EDITORIAL
Diamonds are forever… and so are case reports
Carol L Shields, Jerry A Shields
January-March 2021, 1(1):2-3
DOI:10.4103/ijo.IJO_3737_20  
  471 74 -
OPHTHALMIC IMAGES
Beware of the bruise: Eyelid and periocular cutaneous angiosarcoma
Tarjani V Dave, Richa D Wagh, Dilip K Mishra
January-March 2021, 1(1):6-6
DOI:10.4103/ijo.IJO_1536_20  
  474 63 -
Complete Schwalbe's ring in Axenfeld-Rieger anomaly
Sagarika Snehi, Gaurav Gupta, Deepika Dhingra, Sushmita Kaushik
January-March 2021, 1(1):11-11
DOI:10.4103/ijo.IJO_2268_20  
  460 43 -
Bilateral anterior blue dot and posterior coralliform cataract
Shana Sood, Sanjana Vatsa
April-June 2021, 1(2):163-163
DOI:10.4103/ijo.IJO_1732_20  
  423 68 -
Partial rosette of a traumatic cataract
Anushri P Godbole, Muralidhara Ramappa
April-June 2021, 1(2):164-164
DOI:10.4103/ijo.IJO_3153_20  
  421 66 -
PHOTO ESSAY
An unusual case of recurrent eyelid cysticercosis
Isha K Patel, Divya U Caculo, Trupti M Solu, Shivani Acharya
January-March 2021, 1(1):26-27
DOI:10.4103/ijo.IJO_372_20  
  424 43 -
Neuroretinitis: A rare presentation of optic disc melanocytoma
B Sripathi Kamath, Divya Shenoy, Jaison Velandy, Norman Mendonca
January-March 2021, 1(1):69-70
DOI:10.4103/ijo.IJO_867_20  
  438 25 -
CASE REPORTS
Treatment of 0.01% atropine eye drops induced convergence excess esotropia and rebound myopia managed with 1% atropine eye drops
Shairin Jahan, Mihir Kothari, Meghna Solanki
January-March 2021, 1(1):140-141
DOI:10.4103/ijo.IJO_581_20  
We report a case of progressive childhood myopia who developed rebound myopia and convergence excess esotropia after switching from 1% atropine eye drops to 0.01% atropine eye drops. The esotropia recovered and myopia progression was arrested after stopping 0.01% atropine drops and resuming 1% atropine eye drops.
  422 34 -
A case of old total Descemet membrane detachment due to ophthalmic viscosurgical device with clear cornea: Microscope-integrated intraoperative optical coherence tomography-guided drainage
Nidhi Kalra, Mohamed Ibrahime Asif, Jatinder S Bhalla, Rahul K Bafna, Rajesh Sinha
January-March 2021, 1(1):91-92
DOI:10.4103/ijo.IJO_1740_20  
We report a case of a large bullous descemet membrane detachment (DMD) following inadvertent injection of ophthalmic viscoelastic device in the supradescemetic space. A 27 years old male with juvenile open-angle glaucoma underwent trabeculectomy in the right eye followed by anterior chamber reformation. He developed DMD for which intracameral gas injection failed twice. He presented with complaints of blurring of images in that eye. Examination revealed a bullous DMD without any corneal edema, confirmed by anterior segment optical coherence tomography (ASOCT). Microscope-integrated intraoperative OCT (mi-OCT) guided drainage with intracameral gas injection was done following which the detachment settled completely.
  425 31 -
OPHTHALMIC IMAGES
Vitreous cyst in a 13-year-old girl
Sashwanthi Mohan, Mohan Rajan
January-March 2021, 1(1):18-18
DOI:10.4103/ijo.IJO_1761_20  
  382 64 -
CASE REPORTS
Fractured blood stained steroid implant
Brijesh Takkar, Anushri Prakash Godbole
January-March 2021, 1(1):117-118
DOI:10.4103/ijo.IJO_1200_20  
The usual biodegradation of the sustained release steroid implant does not involve fractures. The case presented in this report was noted to have vitreous haemorrhage staining a steroid implant injected for management of diabetic retinopathy. The implant gradually thinned in the areas adjacent to the haemorrhage, to eventually fracture into 2 pieces. Fracture of the implant is an uncommon event and may be a cause of concern as it can potentially alter the pharmacokinetics/dynamics of the drug.
  410 35 -
OPHTHALMIC IMAGES
Congenital keratopellis
R Balamurugan, Parul Chawla Gupta, Sameer Sethi, Savleen Kaur, Jagat Ram
January-March 2021, 1(1):7-7
DOI:10.4103/ijo.IJO_1822_20  
  386 56 -
CASE REPORTS
Gossypiboma of the eye
Madhu Kumar, Simakurthy Sriram, Ashok Kanakamedla, Jayamadhury Gudimetla, Anurag Shandil, Manit Agrawal
January-March 2021, 1(1):135-136
DOI:10.4103/ijo.IJO_1566_20  
A 50-year-old male patient with proliferative diabetic retinopathy with vitreous hemorrhage underwent vitrectomy with oil tamponade. At 1 week post-operative visit, we noticed a retained cotton fiber with adjacent exudation. Patient was started on oral steroids with a subsequent clearing of exudation within 2 weeks. Inadvertent foreign body implantation after an intraocular surgery occurs more frequently than expected. To date, there is no published report of retained cotton fiber in the vitreous cavity. We present a rare case of pre-retinal retained cotton fiber post-vitrectomy with resultant inflammation and its clinical course.
  392 41 -
A new phenotype of Kartagener's syndrome: An interesting case report
Kalpana Badami Nagaraj, Kavitha L Tumbadi, B Ravi, YD Shilpa, G Bhavna, BC Hemalatha
January-March 2021, 1(1):127-129
DOI:10.4103/ijo.IJO_1645_20  
Kartagener's syndrome (KS) is Primary Ciliary Dyskinesia, autosomal recessive disorder characterised by triad of situs inversus of viscera, sinusitis, bronchiectasis due to ciliary dysfunction. Primary ciliary dyskinesia - retinitis pigmentosa syndrome is an X-linked ciliary dysfunction of respiratory epithelium and photoreceptors of retina leading to ocular disorders associated with chronic bronchiectasis, sinusitis and. sensorineural hearing loss. Here we present one such case of Kartagener's syndrome with Retinitis Pigmentosa (RP) which was also associated with Retinal Detachment (RD) in short stature individual reported for the first time, to the best of our knowledge which could be a new phenotypic presentation in Primary Ciliary Dyskinesia.
  387 32 -