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Inflammatory segmental vitiligo during oral isotretinoin use: a casual association? How to cite this article: Avelar-Caggiano MFS, Castro CCS, Dellatorre G. Inflammatory segmental vitiligo during oral isotretinoin use: a casual association? An Bras Dermatol. 2020;95:399-400. ,☆☆ ☆☆ Study conducted at the Hospital Santa Casa de Misericórdia de Curitiba, Paraná, PR, Brazil.

Segmental vitiligo (SV) accounts for 3-20% of all cases of vitiligo and is usually not associated with autoimmune diseases when compared to non-segmental vitiligo (NSV).11 VanGeel N, Mollet I, Brochez L, Dutré M, De Schepper S, Verhaeghe E, et al. New insights in segmental vitiligo: case report and review of theories. Br J Dermatol. 2011;166:240-6. Among the theories proposed for the path physiology of SV, it is essential to emphasize the presence of an autoimmune attack against a mosaic area.11 VanGeel N, Mollet I, Brochez L, Dutré M, De Schepper S, Verhaeghe E, et al. New insights in segmental vitiligo: case report and review of theories. Br J Dermatol. 2011;166:240-6.

In the literature, there are few reports on the emergence of vitiligo as a side effect of medications, especially oral isotretinoin. The objective of the present report is to demonstrate a possible new side effect of this medication since there are no descriptions of its association with SV in the literature.

A 17 year-old male patient, previously healthy and without a family history of vitiligo, was diagnosed with resistant acne, previously treated with topical and systemic antibiotic therapy. During the fifth month of treatment with oral isotretinoin (0.4 mg/kg/day, cumulative dose of 5.400 mg), there were a chromic spots surrounded by an erythematous-scaling halo in malar and perioral areas, not exceeding the mid line on the right side of the face (Fig. 1). Wood's light examination revealed fluorescent chalky white aspect, as well as polios is in beard hair (Fig. 2) favoring the SV diagnosis. After the withdrawal of isotretinoin, the patient began treatment with 0.1% tacrolimus ointment twice daily with an improvement of perilesional erythema after two months, although without improvement of achromy. Subsequently, it was submitted to 20 sessions of UVB-NB phototherapy, with little perifollicularre pigmentation.

Figure 1
Achromic spots surrounded by halo erythematosus and polios is in beard hairs in the malar and right perioral regions.

Figure 2
Wood's light examination revealed fluoresce bright blue-white in malar and perioral right regions.

In the literature review, only three cases of vitiligo in the context of oral isotretinoin use are described. One report describes the case of a patient who developed vitiligo during the use of oral isotretinoin at a dose of 0.3-0.4 mg/kg/day for the treatment of moderate to severe acne.22 Rao PK, Bhat RM, Nandakishore B, Dandakeri S, Martis J, Kamath GH. Safety and efficacy o flow-dose isotretinoin in the treatment of moderate to severe acne vulgaris. Indian J Dermatol. 2014;59:316. In another report, acrofacial vitiligo was developed only two months after the end of treatment with isotretinoin, which reduces the probability of a cause-and-effect relationship.33 Kokandi AA. Vitiligo appearing after oral isotretinoin therapy for acne. Case Rep Dermatol Med. 2018;2018:1-3. There is also a report of worsening of NSV lesions in the lower lip and lower perioral region after chronic cheilitis due to the use of oral isotretinoin; a condition attributed in this case to the Koebner phenomenon.44 Garner ML, McShane DB, Burkhart CN, Morrell DS. Isotretinoin and vitiligo: canchronic cheilitis cause koebnerization?. Pediatr Dermatol. 2015;32:108-9.

The mechanism of action of isotretinoin in this presumed association is not yet fully elucidated, but the drug appears to play a role in triggering autoimmunity in genetically susceptible individuals.55 Nugroho J, Schweiger B. Isotretinoin as a possible environmental trigger to autoimmunity in genetically susceptible patients. Case Rep Pediatr. 2017;2017:1-3. Several reports of autoimmune diseases such as diabetes, autoimmune hepatitis, Guillain-Barré syndrome, and thyroiditis have been reported after the end of the isotretinoin regimen or during the last week of treatment.55 Nugroho J, Schweiger B. Isotretinoin as a possible environmental trigger to autoimmunity in genetically susceptible patients. Case Rep Pediatr. 2017;2017:1-3. Besides, in vitro studies have also demonstrated that retinoid may have a pro-apoptotic effect on melanocytes.33 Kokandi AA. Vitiligo appearing after oral isotretinoin therapy for acne. Case Rep Dermatol Med. 2018;2018:1-3.

Although the cause-effect relationship of this association has not yet been proven, the increasing appearance of new cases in the literature is a warning sign for dermatologists to keep vigil on this possible new side effect.

  • Financial support
    None declared.
  • How to cite this article: Avelar-Caggiano MFS, Castro CCS, Dellatorre G. Inflammatory segmental vitiligo during oral isotretinoin use: a casual association? An Bras Dermatol. 2020;95:399-400.
  • ☆☆
    Study conducted at the Hospital Santa Casa de Misericórdia de Curitiba, Paraná, PR, Brazil.

References

  • 1
    VanGeel N, Mollet I, Brochez L, Dutré M, De Schepper S, Verhaeghe E, et al. New insights in segmental vitiligo: case report and review of theories. Br J Dermatol. 2011;166:240-6.
  • 2
    Rao PK, Bhat RM, Nandakishore B, Dandakeri S, Martis J, Kamath GH. Safety and efficacy o flow-dose isotretinoin in the treatment of moderate to severe acne vulgaris. Indian J Dermatol. 2014;59:316.
  • 3
    Kokandi AA. Vitiligo appearing after oral isotretinoin therapy for acne. Case Rep Dermatol Med. 2018;2018:1-3.
  • 4
    Garner ML, McShane DB, Burkhart CN, Morrell DS. Isotretinoin and vitiligo: canchronic cheilitis cause koebnerization?. Pediatr Dermatol. 2015;32:108-9.
  • 5
    Nugroho J, Schweiger B. Isotretinoin as a possible environmental trigger to autoimmunity in genetically susceptible patients. Case Rep Pediatr. 2017;2017:1-3.

Publication Dates

  • Publication in this collection
    24 July 2020
  • Date of issue
    May-Jun 2020

History

  • Received
    1 Apr 2019
  • Accepted
    22 July 2019
  • Published
    20 Mar 2020
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