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Dr. Kalyani R

"Journal of Clinical and Diagnostic Research is at present a well-known Indian originated scientific journal which started with a humble beginning. I have been associated with this journal since many years. I appreciate the Editor, Dr. Hemant Jain, for his constant effort in bringing up this journal to the present status right from the scratch. The journal is multidisciplinary. It encourages in publishing the scientific articles from postgraduates and also the beginners who start their career. At the same time the journal also caters for the high quality articles from specialty and super-specialty researchers. Hence it provides a platform for the scientist and researchers to publish. The other aspect of it is, the readers get the information regarding the most recent developments in science which can be used for teaching, research, treating patients and to some extent take preventive measures against certain diseases. The journal is contributing immensely to the society at national and international level."



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Saraswati Dental College
Lucknow
On Sep 2018




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On Aug 2018




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Dr. Arundhathi. S
MBBS, MD (Pathology),
Sanjay Gandhi institute of trauma and orthopedics,
Bengaluru.
On Aug 2018




Dr. Mamta Gupta,
"It gives me great pleasure to be associated with JCDR, since last 2-3 years. Since then I have authored, co-authored and reviewed about 25 articles in JCDR. I thank JCDR for giving me an opportunity to improve my own skills as an author and a reviewer.
It 's a multispecialty journal, publishing high quality articles. It gives a platform to the authors to publish their research work which can be available for everyone across the globe to read. The best thing about JCDR is that the full articles of all medical specialties are available as pdf/html for reading free of cost or without institutional subscription, which is not there for other journals. For those who have problem in writing manuscript or do statistical work, JCDR comes for their rescue.
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An yearly reward for the best article authored can also incentivize the authors. Though the process of finding the best article will be not be very easy. I do not know how reviewing process can be improved. If an article is being reviewed by two reviewers, then opinion of one can be communicated to the other or the final opinion of the editor can be communicated to the reviewer if requested for. This will help one’s reviewing skills.
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Dr. Mamta Gupta
Consultant
(Ex HOD Obs &Gynae, Hindu Rao Hospital and associated NDMC Medical College, Delhi)
Aug 2018




Dr. Rajendra Kumar Ghritlaharey

"I wish to thank Dr. Hemant Jain, Editor-in-Chief Journal of Clinical and Diagnostic Research (JCDR), for asking me to write up few words.
Writing is the representation of language in a textual medium i e; into the words and sentences on paper. Quality medical manuscript writing in particular, demands not only a high-quality research, but also requires accurate and concise communication of findings and conclusions, with adherence to particular journal guidelines. In medical field whether working in teaching, private, or in corporate institution, everyone wants to excel in his / her own field and get recognised by making manuscripts publication.


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Salient features of the JCDR: It is a biomedical, multidisciplinary (including all medical and dental specialities), e-journal, with wide scope and extensive author support. At the same time, a free text of manuscript is available in HTML and PDF format. There is fast growing authorship and readership with JCDR as this can be judged by the number of articles published in it i e; in Feb 2007 of its first issue, it contained 5 articles only, and now in its recent volume published in April 2011, it contained 67 manuscripts. This e-journal is fulfilling the commitments and objectives sincerely, (as stated by Editor-in-chief in his preface to first edition) i e; to encourage physicians through the internet, especially from the developing countries who witness a spectrum of disease and acquire a wealth of knowledge to publish their experiences to benefit the medical community in patients care. I also feel that many of us have work of substance, newer ideas, adequate clinical materials but poor in medical writing and hesitation to submit the work and need help. JCDR provides authors help in this regards.
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In the era of fast growing newer technologies, and in computer and internet friendly environment the manuscripts preparation, submission, review, revision, etc and all can be done and checked with a click from all corer of the world, at any time. Of course there is always a scope for improvement in every field and none is perfect. To progress, one needs to identify the areas of one's weakness and to strengthen them.
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Every one of us: authors, reviewers, editors, and publisher are responsible for enhancing the stature of the journal. I wish for a great success for JCDR."



Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
Strengths of the journal: The journal has an online first facility in which the accepted manuscripts may be published on the website before being included in a regular issue of the journal. This cuts down the time between their acceptance and the publication. The journal is indexed in many databases, though not in PubMed. The editorial board should now take steps to index the journal in PubMed. The journal has a system of notifying readers through e-mail when a new issue is released. Also, the articles are available in both the HTML and the PDF formats. I especially like the new and colorful page format of the journal. Also, the access statistics of the articles are available. The prepublication and the manuscript tracking system are also helpful for the authors.
Areas for improvement: In certain cases, I felt that the peer review process of the manuscripts was not up to international standards and that it should be strengthened. Also, the number of manuscripts in an issue is high and it may be difficult for readers to go through all of them. The journal can consider tightening of the peer review process and increasing the quality standards for the acceptance of the manuscripts. I faced occasional problems with the online manuscript submission (Pre-publishing) system, which have to be addressed.
Overall, the publishing process with JCDR has been smooth, quick and relatively hassle free and I can recommend other authors to consider the journal as an outlet for their work."



Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
E-mail: ravi.dr.shankar@gmail.com
On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
E-mail: anuradha2nittur@gmail.com
On Jan 2020

Important Notice

Images in Medicine
Year : 2026 | Month : September | Volume : 20 | Issue : 9 | Page : NJ01 - NJ03 Full Version

Advanced Double-headed Pterygium with Visual Axis Involvement: A Rare Clinical Presentation


Published: September 1, 2026 | DOI: https://doi.org/10.7860/JCDR/2026/85871.24349
Mohammed Arif Kaderi, Sachin Vishwanath Daigavane

1. Postgraduate Student, Department of Ophthalmology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, Maharashtra, India. 2. Professor and Head, Department of Ophthalmology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, Maharashtra, India.

Correspondence Address :
Dr. Mohammed Arif Kaderi,
Postgraduate Student, Department of Ophthalmology, AVBRH Hospital, Sawangi, Wardha, Maharashtra, India.
E-mail: mkad11@hotmail.com

Keywords

Corneal conjunctivalisation, Grade-IV pterygium, Ocular surface disorder, Pupillary visual axis obstruction

A 68-year-old female reported to the ophthalmology outpatient clinic with symptoms of a fleshy growth in both eyes, along with decrease in vision and foreign body sensation since six months. The patient had no history of diabetes mellitus, hypertension, immunosuppression, or any other systemic disease. There was no prior history of ocular trauma, surgery, or previous pterygium treatment. The patient was not on any long-term medications and reported no family history of similar ocular conditions. Occupational history revealed regular outdoor exposure with significant sunlight and dust exposure. Although the patient reported noticing the lesion and associated symptoms for approximately six months, the clinical appearance suggested that the lesion may have been present for a longer duration before becoming symptomatic.

On examination, the right eye revealed a diheaded Grade-IV pterygium that extended across and covered the pupillary visual axis, as well as conjunctivalisation of the cornea superiorly (Table/Fig 1) (1). At 6 o’clock, a rather clean corneal zone was observed, through which iris tissue could be seen. The pterygium showed significant arborising superficial and deeper feeder arteries, indicating active fibrovascular growth. Visual acuity in the right eye was confined to hand movements close to the face, with perception of light and projection of rays accurately present. The corneal surface above the temporal lesion exhibited an irregular light reflex, indicating secondary stromal scarring and epithelial irregularity.

The left eye had vision of CF2M, not improving with pinhole or refraction. The anterior chamber has normal depth and is quiet, and the lens shows nuclear sclerosis grade 2 with posterior subcapsular cataract. Intraocular pressure measured by applanation tonometry was within normal limits. Posterior segment examination revealed a normal optic disc, macula, and peripheral retina. Refraction or keratometry was not possible due to a high degree of astigmatism. The left eye had a nasal Grade-III pterygium and a temporal Grade-IV pterygium, with the pupillary visual axis being partially spared. Deep feeder vessels were visible, while visual acuity was limited to counting fingers at one metre (Table/Fig 2). Dense leucomatous corneal opacity was seen underneath the pterygium, with irregular stromal remodelling indicating a long-term disease course, potentially related with lipidation, subepithelial fibrosis, and superficial vascular pannus.

The differential diagnosis that was considered was post-infectious corneal scar (bacterial or fungal keratitis), interstitial keratitis, lipid keratopathy, Salzmann nodular degeneration, ocular surface squamous neoplasia, traumatic corneal leukoma, and phlyctenular keratoconjunctivitis. Given the existence of Grade-IV pterygium, pupillary visual axis involvement, and severe vision impairment, particularly in the right eye, advanced (Grade-IV) pterygium with visual axis involvement causing significant vision loss was the final diagnosis. The patient’s treatment strategy included surgical removal of the pterygium. Pterygium excision with conjunctival autografting was proposed as the preferred method for reducing recurrence risk and restoring ocular surface structure. Due to significant visual degradation, the right eye will be treated first, followed by phased operation on the left. Based on intraoperative results, adjunctive procedures such as rigorous fibrovascular tissue excision and anti-fibrotic medications may be used.

As no surgical treatment was performed, the patient will be managed conservatively with topical antibiotics, corticosteroids, and lubricants, along with close monitoring for healing, potential advancement, and visual rehabilitation. Although surgical excision is the definitive treatment for advanced Grade-IV pterygium with visual axis involvement, it was not performed in this case due to patient-related factors.

The patient was thoroughly counselled regarding the need for surgical intervention, including the benefits of visual rehabilitation and prevention of further progression. However, the patient did not consent for immediate surgery due to personal and socio-economic constraints, and preference to defer surgical management at the time of presentation. The prognosis following surgical intervention in such advanced cases is guarded but potentially beneficial, depending on multiple factors; pterygium excision with conjunctival autografting would likely result in improvement in visual acuity, primarily by clearing the visual axis obstruction, reduction in induced astigmatism, although complete normalisation may not occur due to pre-existing corneal irregularity, and restoration of ocular surface anatomy, leading to symptomatic relief.

However, in this particular case, the prognosis is influenced by pre-existing dense stromal scarring and corneal opacity, which may limit visual recovery even after successful excision, long-standing conjunctivalisation, and possible limbal stem cell deficiency, affecting epithelial healing, risk of recurrence, which is higher in large, vascular, and double-headed pterygia despite the use of conjunctival autografting. Thus, while functional and symptomatic improvement is expected, complete visual recovery is unlikely, and the final visual outcome would depend on the extent of irreversible corneal changes. In such advanced cases, additional procedures such as optical keratoplasty may be required for optimal visual rehabilitation. The outcomes of the current conservative management are primarily supportive and symptomatic rather than curative. It is expected to provide relief of symptoms such as irritation, redness, and foreign body sensation, reduction in ocular surface inflammation, improvement in tear film stability and surface comfort, and prevention of secondary infection.

Pterygium is a common degenerative fibrovascular condition of the ocular surface characterised by gradual encroachment of conjunctival tissue onto the cornea, which often originates from the nasal conjunctiva (2). It is usually unilateral and single-headed; however, rare atypical variations like diheaded pterygium, in which fibrovascular tissue spreads onto the cornea from both the nasal and temporal sides, have been identified (3). These unusual forms are frequently more aggressive in character, increasing the risk of visual morbidity caused by rapid progression and substantial corneal involvement. Recurrence is a major concern in advanced pterygium. Studies report recurrence rates of 30-80% with the bare sclera technique, whereas conjunctival autografting significantly reduces recurrence to approximately 5-15%, making it the preferred surgical approach in advanced cases (1),(4).

Grade-IV pterygium is defined by protrusion into or across the pupillary visual axis, which can cause significant vision impairment. Visual loss in these situations is complex and can be caused by severe induced astigmatism, uneven corneal topography, stromal scarring, corneal thinning, or direct obscuration of the visual axis (5). Long-standing injuries may also cause corneal conjunctivalisation, limbal stem cell failure, and chronic ocular surface inflammation, all of which compromise visual results (6). When assessing pterygium, advanced imaging methods like Anterior Segment Optical Coherence Tomography (AS-OCT) might be helpful. By evaluating the depth of corneal invasion, epithelium thickness, and subepithelial fibrovascular tissue, AS-OCT improves lesion characterisation and facilitates surgical planning. Additionally, it can be used to track surgical recovery and distinguish pterygium from other ocular surface diseases. Whereas in this case, Limbal stem cell loss couldn’t be assessed due to advanced stage of disease.

This case showed a bilateral double-headed (diheaded) pterygium with fibrovascular tissue spreading onto the cornea from both nasal and temporal sides, in contrast to the usual appearance of pterygium, which often develops unilaterally from the nasal conjunctiva. Rare and more aggressive, these presentations frequently result in fast corneal invasion and involvement of the pupillary visual axis, which severely impairs vision. Since most documented occurrences of pterygium feature a single head with minimal corneal extension, this case is clinically distinctive due to the lesion’s bilateral and double-headed character. This patient’s profound corneal involvement demonstrates the severity of the condition and its propensity to result in significant visual morbidity.

Long-term environmental and ocular surface risk factors may be linked to bilateral double-headed pterygium. Chronic exposure to Ultraviolet (UV) radiation is thought to be a key aetiological component, particularly for individuals working outside or residing in tropical areas (7). Long-term exposure to wind, dust, dryness, and persistent ocular irritation are other factors that may encourage fibrovascular development and limbal stem cell destruction. These variables may account for the patient’s simultaneous growth of pterygium from both the nasal and temporal sides, which led to considerable corneal involvement and highlighted the case’s uncommon and aggressive character. Reducing progression and recurrence is mostly dependent on prevention. Patients should be encouraged to wear wide-brimmed hats and protective eyewear to reduce UV exposure, particularly in areas with significant sun exposure. In order to reduce ocular surface irritation and prevent the course of the condition, further precautions include the use of lubricating eye drops, protection from wind and dust, and routine ophthalmic follow-up (8).

Surgical treatment of advanced and atypical pterygiums remains difficult. Extensive lesions are linked to higher recurrence rates, more intraoperative difficulties, and a larger risk of postoperative problems (5). To decrease recurrence and restore ocular surface architecture, meticulous surgical technique is required, which may include adjuvant techniques including conjunctival autografting or amniotic membrane transplantation (9). Pre-existing corneal scarring and uneven astigmatism can also hinder visual rehabilitation after surgery, highlighting the significance of early intervention and meticulous postoperative treatment in such complex cases (10).

Adjunctive anti-vascular endothelial growth factor (anti-VEGF) therapy, such as bevacizumab, has been investigated as an adjunct to pterygium surgery and may reduce corneal neovascularisation and the risk of recurrence when administered before or after surgical excision (11). Amniotic membrane transplantation, mitomycin-C administration, and fibrin glue-assisted graft attachment are other cutting-edge techniques that are intended to enhance surgical results and lower recurrence (9).

In this instance, conjunctival autografting was chosen as the ideal surgical approach since it has a lower recurrence rate and produces superior functional and cosmetic results than alternative treatments such as amniotic membrane transplantation or bare sclera excision. Conjunctival autografting reduces postoperative inflammation and fibrovascular regrowth by replacing the scleral defect with healthy conjunctival tissue, which helps repair the ocular surface given the advanced grade of pterygium with visual axis involvement. This method proves to be a better choice for treating severe and aggressive pterygium instances since it also maintains limbal stem cells and creates a more solid ocular surface (1).

References

1.
Shahraki T, Arabi A, Feizi S. Pterygium: An update on pathophysiology, clinical features, and management. Ther Adv Ophthalmol. 2021;13:25158414211020152.[crossref] [PubMed]
2.
Singh SK. Pterygium: Epidemiology prevention and treatment. Community Eye Health. 2017;30(99):S5-S6.
3.
Kurtul BE, Kakac A, Karaaslan A. Bilateral double-headed recurrent pterygium: A case presentation and literature review. Med Hypothesis Discov Innov Ophthalmol. 2020;9(2):85-90.
4.
Xu SC, Chow J, Liu J, Li L, Maslin JS, Chadha N, et al. Risk factors for visual impairment associated with corneal diseases in southern China. Clin Ophthalmol. 2016;10:777-82. Doi: 10.2147/OPTH.S103302.[crossref] [PubMed]
5.
Sarkar P, Tripathy K. Pterygium. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. Available from: https://www.ncbi.nlm.nih.gov/books/NBK558907/.
6.
Bonnet C, Roberts JS, Deng SX. Limbal stem cell diseases. Exp Eye Res. 2021;205:108437. Doi: 10.1016/j.exer.2021.108437.[crossref] [PubMed]
7.
Tandon R, Vashist P, Gupta N, Gupta V, Yadav S, Deka D, et al. The association of sun exposure, ultraviolet radiation effects and other risk factors for pterygium (the SURE RISK for pterygium study) in geographically diverse adult (≥40 years) rural populations of India – 3rd report of the ICMR-EYE SEE study group. PLoS One. 2022;17(7):e0270065. Doi: 10.1371/journal. pone.0270065.[crossref] [PubMed]
8.
Katipog? lu Z, Zengin N. Dust exposure: A novel environmental risk factor for conjunctivochalasis? Ther Adv Ophthalmol. 2021;13:25158414211027757.[crossref] [PubMed]
9.
Rosen R. Amniotic membrane grafts to reduce pterygium recurrence. Cornea. 2018;37(2):189-93. Doi: 10.1097/ICO.0000000000001407.[crossref] [PubMed]
10.
Chandran C, Santra M, Rubin E, Geary ML, Yam GH. Regenerative therapy for corneal scarring disorders. Biomedicines. 2024;12(3):649. Doi: 10.3390/ biomedicines12030649.[crossref] [PubMed]
11.
Nuzzi R, Tridico F. Efficacy of subconjunctival bevacizumab injections before and after surgical excision in preventing pterygium recurrence. J Ophthalmol. 2017;2017:4131735. Doi:10.1155/2017/4131735.[crossref]

DOI and Others

DOI: 10.7860/JCDR/2026/85871.24349

Date of Submission: Dec 14, 2025
Date of Peer Review: Mar 05, 2026
Date of Acceptance: Jun 17, 2026
Date of Publishing: Sep 01, 2026

Author declaration:
• Financial or Other Competing Interests: None
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. Yes

PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Mar 03, 2026
• Manual Googling: Jun 13, 2026
• iThenticate Software: Jun 15, 2026 (2%)

ETYMOLOGY: Author Origin

EMENDATIONS: 6

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