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chest&#44; and shoulders&#44; which had not responded to prior treatment with HMBE &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">An 88&#37; aqueous solution of phenol was applied selectively&#44; starting on the pigmented areas on the right cheek&#44; as they were small areas that minimized systemic absorption&#44; toxicity&#44; and adverse effects&#46; This was achieved by evaluating the response and tolerance of the patients and by applying cold compresses to alleviate pain immediately after frosting was observed&#46; Given the good response&#44; 4 applications were performed on the same section&#44; achieving complete depigmentation&#44; and the same procedure was performed on the other pigmented areas with excellent results and no evidence of repigmentation until 1&#8239;year after the procedure&#59; the patient&#44; who complied strictly with photoprotection&#44; was very satisfied &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">The melanotoxic effects of phenol have been previously documented&#44; but its depigmenting mechanism of action appears to be complex&#46; The common characteristic of these products is their chemical structure&#44; which includes a phenol group made up of a benzene ring with a hydroxyl side chain&#44; a structure that is shared with the amino acid tyrosine&#46; Potent phenols act as tyrosine analogs&#44; interfering with the melanogenesis pathway&#44; and initial hypotheses suggested that depigmenting chemicals that entered the melanogenesis pathway generated toxic metabolites that destroy the melanocytes&#46; Tyrosine and other enzymes of melanogenesis bind covalently to phenols&#44; as does tyrosine&#44; generating reactive oxygen species and activating the response of the proteins released&#44; autophagy&#44; and exosomes&#44; which supply adjacent immune cells with new antigens&#44; initiate an inflammatory response&#44; and activate autoreactive T cells&#44; thus initiating an autoimmune response that results in their destruction&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">They also induce glutathione depletion&#44; which may increase the immunogenicity of melanosomal proteins&#46; The pigmented cells exposed to phenol activate specific T cells&#44; also reacting against other melanocytes not directly stressed by exposure&#46; This would explain depigmentation at a distance from these compounds through a mechanism analogous to that which occurs in contact sensitization&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The use of phenol has not been described previously in guidelines on the management of vitiligo&#44; even though its use may be safe and economically viable&#46; In Brazil&#44; however&#44; it has been introduced successfully in clinical practice at a concentration of 88&#37;&#44; as a depigmenting therapy for universal vitiligo&#59; nevertheless&#44; a case reported in Iran obtained no response to single-drug therapy with phenol and treatment was supplemented with cryotherapy&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5&#44;6</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Phenol is an aromatic hydrocarbon derived from coal tar and is used as a chemical peeling agent&#46; Its effect varies depending on the concentration and the surface area to which it is applied&#46; Concentrations above 80&#37; produce denaturalization and rapid and irreversible coagulation of epidermal proteins&#44; resulting in the formation of a barrier that prevents the chemical from penetrating the deep dermis&#44; whereas when diluted to 50&#37;&#44; it acts as a keratolytic agent and disrupts the sulfur bridges&#44; thus increasing its penetration beyond the dermis and causing greater destruction and systemic absorption&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Complications may include scarring&#44; dyschromia&#44; and eczema herpeticum&#46; High doses are toxic&#44; and it must not&#44; therefore&#44; be applied over large areas&#44; given that it has a marked corrosive action&#44; either due to ingestion&#44; inhalation&#44; or direct contact&#46; Cellular uptake is rapid and passive due to its lipophilic nature and signs of systemic toxicity appear shortly after exposure&#46; Target organs are the liver&#44; kidneys&#44; lungs&#44; and cardiovascular system&#46; When used by qualified experts&#44; however&#44; it does not usually cause complications&#46; Repigmentation of the skin may occur if patients do not protect themselves adequately from the sun&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Although the only treatment currently approved by the US Food and Drugs Administration &#40;FDA&#41; 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Case and Research Letters
Residual Pigment Islands Treated With 88% Phenol Peeling in a Woman With Universal Vitiligo
Islotes de pigmentación residual en paciente con vitiligo universal, tratados con peeling de fenol al 88%
A. Alomara,
Corresponding author
Agustin.alomar@quironsalud.es

Corresponding author.
, M. Marrón Hernándezb, F. Bittencourtc
a Universidad Autónoma de Barcelona, Clínica Dermatológica Moragas, Barcelona, Spain
b Universidad Central de Venezuela, Cursante del Máster de Dermatología Avanzada de la Universidad Autónoma de Barcelona, Barcelona, Spain
c Faculdade de Medicina do ABC, Cursante del Máster de Dermatología Avanzada de la Universidad Autónoma de Barcelona, Barcelona, Spain
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    "titulo" => "Residual Pigment Islands Treated With 88&#37; Phenol Peeling in a Woman With Universal Vitiligo"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Vitiligo is a depigmenting skin disease with a global prevalence of 1&#37;&#46; While multiple therapeutic options exist&#44; none of them is completely satisfactory&#44; especially in universal vitiligo&#44; where depigmentation of the residual areas of pigment using chemical methods&#44; such as hydroquinone monobenzyl ether &#40;HMBE&#41;&#44; may be cosmetically acceptable&#44; as it produces complete&#44; almost irreversible depigmentation&#46; Other depigmenting substances exist&#44; however&#44; such as phenol&#44; have been described previously but with little clinical evidence&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 67-year-old woman with vitiligo that had appeared in childhood and was universally distributed since 14 years earlier visited our department seeking alternative depigmenting therapeutic options&#44; as she presented areas of residual pigmentation on the face&#44; chest&#44; and shoulders&#44; which had not responded to prior treatment with HMBE &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">An 88&#37; aqueous solution of phenol was applied selectively&#44; starting on the pigmented areas on the right cheek&#44; as they were small areas that minimized systemic absorption&#44; toxicity&#44; and adverse effects&#46; This was achieved by evaluating the response and tolerance of the patients and by applying cold compresses to alleviate pain immediately after frosting was observed&#46; Given the good response&#44; 4 applications were performed on the same section&#44; achieving complete depigmentation&#44; and the same procedure was performed on the other pigmented areas with excellent results and no evidence of repigmentation until 1&#8239;year after the procedure&#59; the patient&#44; who complied strictly with photoprotection&#44; was very satisfied &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">The melanotoxic effects of phenol have been previously documented&#44; but its depigmenting mechanism of action appears to be complex&#46; The common characteristic of these products is their chemical structure&#44; which includes a phenol group made up of a benzene ring with a hydroxyl side chain&#44; a structure that is shared with the amino acid tyrosine&#46; Potent phenols act as tyrosine analogs&#44; interfering with the melanogenesis pathway&#44; and initial hypotheses suggested that depigmenting chemicals that entered the melanogenesis pathway generated toxic metabolites that destroy the melanocytes&#46; Tyrosine and other enzymes of melanogenesis bind covalently to phenols&#44; as does tyrosine&#44; generating reactive oxygen species and activating the response of the proteins released&#44; autophagy&#44; and exosomes&#44; which supply adjacent immune cells with new antigens&#44; initiate an inflammatory response&#44; and activate autoreactive T cells&#44; thus initiating an autoimmune response that results in their destruction&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">They also induce glutathione depletion&#44; which may increase the immunogenicity of melanosomal proteins&#46; The pigmented cells exposed to phenol activate specific T cells&#44; also reacting against other melanocytes not directly stressed by exposure&#46; This would explain depigmentation at a distance from these compounds through a mechanism analogous to that which occurs in contact sensitization&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The use of phenol has not been described previously in guidelines on the management of vitiligo&#44; even though its use may be safe and economically viable&#46; In Brazil&#44; however&#44; it has been introduced successfully in clinical practice at a concentration of 88&#37;&#44; as a depigmenting therapy for universal vitiligo&#59; nevertheless&#44; a case reported in Iran obtained no response to single-drug therapy with phenol and treatment was supplemented with cryotherapy&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5&#44;6</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Phenol is an aromatic hydrocarbon derived from coal tar and is used as a chemical peeling agent&#46; Its effect varies depending on the concentration and the surface area to which it is applied&#46; Concentrations above 80&#37; produce denaturalization and rapid and irreversible coagulation of epidermal proteins&#44; resulting in the formation of a barrier that prevents the chemical from penetrating the deep dermis&#44; whereas when diluted to 50&#37;&#44; it acts as a keratolytic agent and disrupts the sulfur bridges&#44; thus increasing its penetration beyond the dermis and causing greater destruction and systemic absorption&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Complications may include scarring&#44; dyschromia&#44; and eczema herpeticum&#46; High doses are toxic&#44; and it must not&#44; therefore&#44; be applied over large areas&#44; given that it has a marked corrosive action&#44; either due to ingestion&#44; inhalation&#44; or direct contact&#46; Cellular uptake is rapid and passive due to its lipophilic nature and signs of systemic toxicity appear shortly after exposure&#46; Target organs are the liver&#44; kidneys&#44; lungs&#44; and cardiovascular system&#46; When used by qualified experts&#44; however&#44; it does not usually cause complications&#46; Repigmentation of the skin may occur if patients do not protect themselves adequately from the sun&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Although the only treatment currently approved by the US Food and Drugs Administration &#40;FDA&#41; for vitiligo is HMBE&#44; few published cases describing the efficacy of phenol and isolated studies demonstrating its mechanism of action exist&#46; Our patient presented a satisfactory response to the selective application of 88&#37; phenol&#44; with no complications and no relapse&#59; we therefore consider it to be an excellent depigmenting therapeutic option in universal vitiligo with areas of pigmentation that do not respond to HMBE&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Funding</span><p id="par0050" class="elsevierStylePara elsevierViewall">This study has not received funding of any kind&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflicts of Interest</span><p id="par0055" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Alomar A&#44; Marr&#243;n Hern&#225;ndez M&#44; Bittencourt F&#46; Islotes de pigmentaci&#243;n residual en paciente con vitiligo universal&#44; tratados con <span class="elsevierStyleItalic">peeling</span> de fenol al 88&#37;&#46; Actas Dermosifiliogr&#46; 2021&#59;112&#58;284&#8211;285&#46;</p>"
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Article information
ISSN: 15782190
Original language: English
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Idiomas
Actas Dermo-Sifiliográficas
es en

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