|LETTER TO THE EDITOR
|Year : 2019 | Volume
| Issue : 6 | Page : 731-734
Ocular abnormalities in vitiligo patients: A cross-sectional study
Neel Prabha1, Namrata Chhabra1, Ankur Kumar Shrivastava2, Ripu Daman Arora3, VR Roja4, Shrikant Kaushik2, Nitin M Nagarkar4
1 Department of Dermatology and Venereology, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India
2 Department of Ophthalmology, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India
3 Department of ENT and HNS, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India
4 Department of ICMR, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India
|Date of Web Publication||1-Nov-2019|
Ripu Daman Arora
All India Institute of Medical Sciences, GE Rd, Tatibandh, Raipur, Chhattisgarh
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Prabha N, Chhabra N, Shrivastava AK, Arora RD, Roja V R, Kaushik S, Nagarkar NM. Ocular abnormalities in vitiligo patients: A cross-sectional study. Indian Dermatol Online J 2019;10:731-4
|How to cite this URL:|
Prabha N, Chhabra N, Shrivastava AK, Arora RD, Roja V R, Kaushik S, Nagarkar NM. Ocular abnormalities in vitiligo patients: A cross-sectional study. Indian Dermatol Online J [serial online] 2019 [cited 2021 Dec 2];10:731-4. Available from: https://www.idoj.in/text.asp?2019/10/6/731/270211
Vitiligo is an acquired discoloration of the skin caused by epidermal melanocyte loss or damage. Various studies have found the association of ocular abnormalities with vitiligo.,,,,,, We studied 52 clinically diagnosed vitiligo patients. Pregnant females, patients with history or evidence of ocular trauma, and systemic diseases such as diabetes, hypertension etc. were excluded. A complete ophthalmologic examination was conducted by an ophthalmologist. Detailed ocular examinations included best corrected visual acuity assessment, refraction, external examination with torchlight and slit lamp biomicroscopy, gonioscopy, and dilated fundus examination with 90 D lens. The data was summarized using descriptive statistics, frequencies, and percentage. Statistical differences between categorical variables were assessed using the Chi-square test. A P value <0.05 was considered statistically significant.
There were 28 males and 24 females in the study. The mean age of the patients was 26.7 years ranging from 7 years to 60 years. The mean age of onset of vitiligo was 21.7 years ranging from 4 years to 50 years. Eight patients (15.3%) had a positive family history and included first-degree relatives in 4 (7.6%), second-degree relatives in 3 (5.7%) patients, and both first and second degree relatives in 1 (1.9%) patient. The majority of [51 (96%)] patients had non-segmental vitiligo. Vitiligo vulgaris was the most common (36.5%) clinical type followed by acrofacial (19.2%), facial (17.3%), acral (13.5%), focal (5.8%), vitiligo universalis (3.8%), mucosal (1.9%), and segmental (1.9%). The usual site of onset was head and neck in 22 (42.3%), lower limbs in 12 (23%), upper limbs in 9 (17.3%), trunk in 6 (11.5%), and mucosa in 3 (5.8%) patients. Body surface area involvement was <50% in 50 (96.2%) patients and only 2 (3.8%) patients had universal vitiligo.
Ophthalmologic examination was done in all patients. Eighteen patients (34.6%) had periocular depigmentation. Poliosis was seen in 3 (5.7%) patients [Figure 1]. Details of vitiligo patients with ocular findings are given in [Table 1]. Hypopigmented trabecular meshwork was seen in 5 (9.6%) patients, and one patient of these 5 patients had hypopigmented ciliary body also. Four of these 5 patients had periocular depigmentation. Statistically, significant association was found between periocular depigmentation and hypopigmented trabecular meshwork (P value 0.018). [Table 2] and [Figure 2]a, b] One patient had retinitis pigmentosa and periocular depigmentation. Relation between age, age at the onset, gender, periorbital depigmentation, and clinical type with ocular involvement is shown in [Table 3]. Most cases of ocular findings were detected in age group 1–20 years (26.3%). Ocular findings were present in 1 (6.7%) out of 14 patients having vitiligo for less than 5 years and 5 out of 32 (13.5%) having vitiligo for more than 5 years (P value 0.659). Statistically, significant association was found between periorbital depigmentation, (P value 0.005) and facial vitiligo (P value 0.019) with ocular findings.
|Table 2: Association of periocular depigmentation with hypopigmented trabecular meshwork|
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|Figure 2: (a) Periorbital vitiligo. (b) Gonioscopy of same patient showing hypopigmented trabecular meshwork (black arrow)|
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|Table 3: Ocular findings in relation to age, age of onset, sex, periorbital depigmentation, and clinical type|
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In addition to the skin, melanocytes are found in the retinal pigment epithelium (RPE) and the uveal tract. Melanocytes present in the choroid are responsible for constitutive eye pigmentation and protection against ultraviolet radiation. These cells are important for the degradation of toxic factors. The retinal pigment epithelium is formed by a distinct type of melanocytes as the outermost layer of the retina. These melanocytes are involved in the metabolism of retinoids and rod outer segments and play a major role in vision. In vitiligo, mechanisms responsible for melanocyte destruction in the skin can affect melanocytes within iris and retina of the eyes as well.
There is well-known association of vitiligo with ocular disturbances in diseases such as Vogt-Koyanagi-Harada syndrome More Details and Alezzandrini's syndrome. In Vogt-Koyanagi-Harada syndrome, vitiligo, poliosis, uveitis, alopecia, neurological, and auditory findings (meningismus and tinnitus) are seen. In Alezzandrini's syndrome, unilateral facial vitiligo, white hair, poliosis, unilateral retinal degeneration, and deafness are seen. Depigmentation of the eyelids and poliosis of the eyebrows and eyelashes are commonly seen in vitiligo. Uveitis has been reported in 4.8–19% of patients with vitiligo.,,, Various fundal pigment disturbances described in vitiligo includes pigment clumps, focal hypopigmented spots, diffuse hypopigmentation, diffuse, focal, or sectoral atrophy of the RPE, or chorioretinal scars, choroidal nevi.,, Ring-like peripapillary atrophy around the optic nerve was also observed., There are some isolated reports of vitiligo occurring with tapetoretinal degeneration., Hypopigmented spots on the iris and angle, iris atrophy, heterochromic iris and pigmentation in anterior chamber were also noted.,, However, we could not find any of the above fundus/iris findings in our study except one patient with retinitis pigmentosa. We found a statistically significant finding of hypopigmented trabecular meshwork in periorbital vitiligo. Retinitis pigmentosa and retinitis pigmentosa-like syndromes are seen sporadically in patients with vitiligo, but the relationship between vitiligo and retinitis pigmentosa is difficult to assess., Albert et al. postulated that on rare occasions there may be sufficient RPE degeneration to produce a retinitis pigmentosa-like syndrome in vitiligo. In the present study, one patient with periorbital vitiligo had retinitis pigmentosa. Vitiligo patients can be more prone to dry eye syndrome as well. However, in the present study, we have not done Schirmer's test to evaluate dry eye. As few studies showed a risk of dry eye in vitiligo, Schirmer's test may also be included in ocular examination in vitiligo.
The connection between the anatomic localization of vitiligo and ocular findings was also studied by various authors. Rosenbaum et al. reported an association between bilateral changes in the RPE with periorbital vitiligo and seizures. Wagoner et al. suggested that periocular skin depigmentation is a frequent abnormality in patients with ocular findings. Baskan et al. reported that ocular findings are primarily associated with periorbital and, to a lesser extent, genital vitiligo. Pai et al. found that iris and fundus changes were maximum in cases with lesions located on the face, and angle changes were more significant in cases with genital vitiligo. In the present study, a significant association (P value 0.005) between periorbital depigmentation and ocular findings was found.
In the present study, except one retinitis pigmentosa patient, none of the other patients complained of visual impairment. Retinitis pigmentosa patient had decreased visual acuity, and other patients had normal visual acuity. This is in corroboration with the study of Nordunt et al. and Pai et al., The lack of symptoms can be explained by the location of the destructive lesions, which lie in the periphery and not near the macula. We could not find significant association between ocular findings in vitiligo with age, gender, age at the onset of disease, and disease duration; these results are in agreement with the findings of Baskan et al. and Pai et al.,
Although the clinical relevance of these ocular findings is unclear, there are some medicolegal implications as ocular changes can develop with steroids and phototherapy. Doria et al. studied ocular changes in vitiligo patients treated with oral Photochemotherapy with psoralen using natural sunlight (PUVASOL). Discrete dusty, golden, yellow deposits were noticed in cornea and lens after 6 months of therapy. Reversible visual acuity changes were seen. Fundus showed dull macular degeneration in patients above 30 years of age. Shah recommended that for medicolegal implications, baseline documentation prior to starting phototherapy or applying topical steroids around the eyes is important, especially in a patient with periorbital vitiligo.
To conclude, there is a significant association of facial vitiligo and periorbital vitiligo with ocular findings. Hence, ocular examination should be a part of routine workup, especially if vitiligo lesions involve head and neck region. For medicolegal implications also, before starting phototherapy or applying topical steroids around eyes, baseline documentation of eye examination is important, especially in periorbital vitiligo cases. Future prospective studies, evaluating the progression of ophthalmic findings and its correlation with vitiligo need to be done.
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| References|| |
Albert DM, Nordlund JJ, Lerner AB. Ocular abnormalities occurring with vitiligo. Ophthalmology 1979;86:1145-60.
Albert DM, Wagoner MD, Pruett RC, Nordlund JJ, Lerner AB. Vitiligo and disorders of the retinal pigment epithelium. Br J Ophthalmol 1983;67:153-6.
Lerner AB, Kirkwood J, Forget BM, Nordlund JJ. New observations on vitiligo and ocular disease. Am J Ophthalmol 1983;96:16-26.
Cowan CL Jr, Halder RM, Grimes PE, Chakrabarti SG, Kenney JA Jr. Ocular disturbances in vitiligo. J Am Acad Dermatol 1986;15:17-24.
Biswas G, Barbhuiya JN, Biswas MC, Islam MN, Dutta S. Clinical pattern of ocular manifestations in vitiligo. J Indian Med Assoc 2003;101:478-80.
Bulbul Baskan E, Baykara M, Ercan I, Tunali S, Yucel A. Vitiligo and ocular findings: A study on possible associations. J Eur Acad Dermatol Venereol 2006;20:829-33.
Karadag R, Esmer O, Karadag AS, Bilgili SG, Cakici O, Demircan YT, et al.
Evaluation of ocular findings in patients with vitiligo. Int J Dermatol 2016;55:351-5.
Cieścińska C, Pawlak-Osińska K, Marzec M, Kaźmierczak K, Malukiewicz G, Drewa G, et al.
Prevalence of impaired hearing and vision in patients with vitiligo. Acta Dermatovenerol Croat 2016;24:20-4.
Anstey AV. Diorders of skin colour. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook's Textbook of Dermatology. 8th
ed. UK: Wiley-Blackwell; 2010. p. 58.1-58.57.
Baskan EB, Baykara M, Ercan I, Tunali S, Yucel A. Vitiligo and ocular findings: A study on possible associations. J Eur Acad Dermatol Venereol 2006;20:829-33.
Wagoner MD, Albert DM, Lerner AB, Kirkwood J, Forget BM, Nordlund JJ. New observations on vitiligo and ocular disease. Am J Ophthalmol 1983;96:16-26.
Gordon DM. Retinitis pigmentosa associated with vitiligo of the skin. Arch Ophthalmol 1953;50:372-4.
Merz M, Szigielski M, Langucki J. Unilateral sectorial pigmentary degeneration and vitiligo. Ophthalmologica 1969;157:357-61.
Pai SG, Gupta A, Dudeja L, Nayak MK. Ocular Manifestations of vitiligo: Evaluation and study of any possible association. Online J Health Allied Scs 2015;14:10.
Gopal KV, RamaRao GR, Kumar YH, AppaRao MV, Vasudev P, Srikant. Vitiligo: A part of a systemic autoimmune process. Indian J Dermatol Venereol Leprol 2007;73:162-5.
] [Full text]
Rosenbaum J, Bunke A, Cooperman E, Gombos GM. Bilateral retinal pigment epithelium changes associated with periorbitalvitiligo and seizure disorders. Ann Ophthalmol 1979;11:1191-3.
Nordlund JJ, Lerner AB. Vitiligo. It is important. Arch Dermatol 1982;118:5-8.
Doria R, Bhargava R. A study of ocular findings in vitiligo patients treated with PUVASOL. Indian J Dermatol Venereol Leprol 1991;57:135-7. [Full text]
Shah MK. Ocular abnormalities in childhood vitiligo – When to screen? Indian J Paediatr Dermatol 2017;18:351-2. [Full text]
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]