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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Facial discoid dermatosis &#40;FDD&#41; is a recently described condition<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> that differs from other facial dermatoses in its clinical appearance and histopathologic findings&#8212;which mimic those of pityriasis rubra pilaris &#40;PRP&#41;&#8212;as well as in its failure to respond to treatment&#46; We describe a characteristic case of FDD&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 61-year-old man with no remarkable past medical history presented with 3 intensely pruriginous lesions that had appeared 2 months before&#46; He had tried antihistamines&#44; corticosteroids&#44; antibiotics&#44; and topical antifungal creams without seeing improvement&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Physical examination showed a salmon-colored erythematous plaque with thick yellowish&#44; adherent scaling&#46; The plaque in the left malar region measured approximately 3<span class="elsevierStyleHsp" style=""></span>cm in diameter and affected the lower eyelid&#46; Two other similar but smaller plaques were observed&#46; They were circular and on the right side of the nose&#46; Involvement of the eyelid progressed and eventually caused marked ectropion &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Two biopsies were performed for histopathology &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>a and b&#41;&#46; The results of laboratory analyses &#40;a full blood work-up including biochemistry&#44; immunoglobulins&#44; and antibodies&#41; were normal or negative&#44; as were patch tests&#46; Successive treatments with clobetasol&#44; prednisone&#44; hydroxychloroquine&#44; and methotrexate were ineffective&#46; Despite poor control of the skin disease&#44; the consulting ophthalmologists scheduled surgical ectropion repair&#46; However&#44; the procedure was not performed because 2 months after the last treatment prescribed &#8212; an ointment containing calcipotriol plus betamethasone to be applied at night &#8212; all symptoms resolved &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; At the time of writing a year later&#44; the patient was applying a 0&#46;1&#37; tacrolimus cream twice a week because repeated attempts to stop treatment altogether were followed by relapses&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">FDD is characterized by macules&#44; papules&#44; or well-defined plaques on the face&#46; The lesions are circular&#44; pink-orange in color&#44; and develop adherent scales&#46; The clinical course is chronic and refractory to treatment&#46; The number and size of lesions vary&#44; and cases have been described over a wide range of ages from infancy to the sixth decade of life&#44; usually in females&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">1&#8211;4</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The initial description of FDD listed features that were nonspecific but suggestive of PRP&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> Histopathologic features included psoriasiform acanthosis&#44; hyperkeratosis with parakeratosis&#44; and follicular plugs&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> Later additions to the description included spongiosis&#44;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">2&#44;4</span></a> a perivascular lymphocytic infiltrate that spared skin adnexa&#44;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">3&#44;4</span></a> alternating orthohyperkeratosis and parakeratosis forming a checkerboard pattern with a conserved or prominent granular layer&#44; subcorneal acantholysis&#44; and vacuoled keratinocytes&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">One of the defining characteristics of FDD is its chronic course and resistance to numerous treatments&#44; such as corticosteroids &#40;topical&#44; intralesional&#44; and systemic&#41;&#44; calcitriol&#44; tacrolimus&#44; pimecrolimus&#44; tazarotene&#44; imiquimod&#44; tretinoin&#44; topical and oral antifungal medications&#44; hydroxychloroquine&#44; doxycycline&#44; methotrexate&#44; phototherapy&#44; and pulsed light therapy&#46; The combination of betamethasone dipropionate with oral acitretin was reported to lead to the greatest improvement&#44; but it still failed to achieve complete clearance&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> We report remarkably good results achieved in our patient with the combination of betamethasone and calcipotriol without acitretin&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">The differential diagnosis includes other facial skin diseases such as psoriasis&#44; lupus&#44; seborrheic dermatitis contact dermatitis&#44; rosacea&#44; Demodex mite infestation&#44; mycosis fungoides&#44; and seborrheic pemphigus&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">1&#44;4</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Since the first description of this condition by Ko et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> the possibility that FDD is related to PRP has been hypothesized&#46; Clinical manifestations &#40;salmon-colored plaques with adherent scaling&#41;&#44; a prolonged course of disease that is resistant to treatment&#44; and compatible histopathologic findings were the arguments put forward by these authors&#44; who wondered whether FDD was an independent entity or a new localized form of PRP&#44; possibly a seventh phenotype&#46; Additional traits noted since then suggest that FDD and PRP are indeed closely related&#46; The presence of alternating orthohyperkeratosis and parakeratosis&#44; for example&#44; as well as subcorneal acantholysis&#44; and vacuoled keratinocytes are histopathologic findings that are characteristic of both processes&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">4&#44;5</span></a> Gan et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> therefore also suggested that FDD could be an incomplete form of PRP&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">PRP is one of the few skin diseases that can lead to ectropion&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">6&#44;7</span></a> Classical adult onset PRP&#44; the most severe form&#44; might put patients at greatest risk of this complication&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">6</span></a> Our patient&#39;s unilateral ectropion&#44; which was closely associated with the type and timing of the skin lesions&#44; 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and tends to have a prolonged chronic course&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">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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Vol. 113. Issue 7.
Pages T728-T731 (July - August 2022)
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Vol. 113. Issue 7.
Pages T728-T731 (July - August 2022)
Case and Research Letter
Open Access
Facial Discoid Dermatosis: A New Variant of Pityriasis Rubra Pilaris?
Dermatosis discoide facial: ¿una nueva forma de pitiriasis rubra pilaris?
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F. Alleguea,
Corresponding author
fallegue@mundo-r.com

Corresponding author.
, C. Fachalb, B. Iglesiasb, A. Zulaicaa
a Servicio de Dermatología, Hospital do Meixoeiro, EOXI, Vigo, Pontevedra, Spain
b Servicio de Anatomía Patológica, Hospital Álvaro Cunqueiro, EOXI, Vigo, Pontevedra, Spain
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Actas Dermosifiliogr. 2022;113:728-3110.1016/j.ad.2021.01.006
F. Allegue, C. Fachal, B. Iglesias, A. Zulaica
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To the Editor:

Facial discoid dermatosis (FDD) is a recently described condition1 that differs from other facial dermatoses in its clinical appearance and histopathologic findings—which mimic those of pityriasis rubra pilaris (PRP)—as well as in its failure to respond to treatment. We describe a characteristic case of FDD.

A 61-year-old man with no remarkable past medical history presented with 3 intensely pruriginous lesions that had appeared 2 months before. He had tried antihistamines, corticosteroids, antibiotics, and topical antifungal creams without seeing improvement.

Physical examination showed a salmon-colored erythematous plaque with thick yellowish, adherent scaling. The plaque in the left malar region measured approximately 3cm in diameter and affected the lower eyelid. Two other similar but smaller plaques were observed. They were circular and on the right side of the nose. Involvement of the eyelid progressed and eventually caused marked ectropion (Fig. 1). Two biopsies were performed for histopathology (Fig. 2a and b). The results of laboratory analyses (a full blood work-up including biochemistry, immunoglobulins, and antibodies) were normal or negative, as were patch tests. Successive treatments with clobetasol, prednisone, hydroxychloroquine, and methotrexate were ineffective. Despite poor control of the skin disease, the consulting ophthalmologists scheduled surgical ectropion repair. However, the procedure was not performed because 2 months after the last treatment prescribed — an ointment containing calcipotriol plus betamethasone to be applied at night — all symptoms resolved (Fig. 3). At the time of writing a year later, the patient was applying a 0.1% tacrolimus cream twice a week because repeated attempts to stop treatment altogether were followed by relapses.

Figure 1.

Three salmon-colored, discoid facial lesions with thick scaling. The largest one involved the lower eyelid and progressed to cause ectropion. A and B, Presentation at the first clinical visit. C, Presentation 2 months later. D–F, Presentation 7 months later.

(0.39MB).
Figure 2.

A) Epidermal hyperplasia with marked keratotic spikes in the follicular ostium and parakeratosis that is accentuated in the region surrounding the follicular infundibulum. The lymphocytic infiltrate is perivascular in the dermis. Hematoxylin–eosin (H&E) staining, magnification ×40. B) Evident epidermal acanthosis with hyperkeratosis, corneal plugs, and parakeratosis often located around follicles. Munro abscesses were not observed. Thickening of the granular layer and mild spongiosis with lymphocytic exocytosis. Perivascular lymphocytic infiltrate in the dermis. There is basophilic degeneration of collagen, without increased mucin deposition. H&E staining, magnification ×100.

(0.4MB).
Figure 3.

Resolution of the patient's facial discoid dermatosis after treatment with betamethasone plus calcipotriol.

(0.13MB).

FDD is characterized by macules, papules, or well-defined plaques on the face. The lesions are circular, pink-orange in color, and develop adherent scales. The clinical course is chronic and refractory to treatment. The number and size of lesions vary, and cases have been described over a wide range of ages from infancy to the sixth decade of life, usually in females.1–4

The initial description of FDD listed features that were nonspecific but suggestive of PRP.1 Histopathologic features included psoriasiform acanthosis, hyperkeratosis with parakeratosis, and follicular plugs.1 Later additions to the description included spongiosis,2,4 a perivascular lymphocytic infiltrate that spared skin adnexa,3,4 alternating orthohyperkeratosis and parakeratosis forming a checkerboard pattern with a conserved or prominent granular layer, subcorneal acantholysis, and vacuoled keratinocytes.4

One of the defining characteristics of FDD is its chronic course and resistance to numerous treatments, such as corticosteroids (topical, intralesional, and systemic), calcitriol, tacrolimus, pimecrolimus, tazarotene, imiquimod, tretinoin, topical and oral antifungal medications, hydroxychloroquine, doxycycline, methotrexate, phototherapy, and pulsed light therapy. The combination of betamethasone dipropionate with oral acitretin was reported to lead to the greatest improvement, but it still failed to achieve complete clearance.3 We report remarkably good results achieved in our patient with the combination of betamethasone and calcipotriol without acitretin.

The differential diagnosis includes other facial skin diseases such as psoriasis, lupus, seborrheic dermatitis contact dermatitis, rosacea, Demodex mite infestation, mycosis fungoides, and seborrheic pemphigus.1,4

Since the first description of this condition by Ko et al.,1 the possibility that FDD is related to PRP has been hypothesized. Clinical manifestations (salmon-colored plaques with adherent scaling), a prolonged course of disease that is resistant to treatment, and compatible histopathologic findings were the arguments put forward by these authors, who wondered whether FDD was an independent entity or a new localized form of PRP, possibly a seventh phenotype. Additional traits noted since then suggest that FDD and PRP are indeed closely related. The presence of alternating orthohyperkeratosis and parakeratosis, for example, as well as subcorneal acantholysis, and vacuoled keratinocytes are histopathologic findings that are characteristic of both processes.4,5 Gan et al.4 therefore also suggested that FDD could be an incomplete form of PRP.

PRP is one of the few skin diseases that can lead to ectropion.6,7 Classical adult onset PRP, the most severe form, might put patients at greatest risk of this complication.6 Our patient's unilateral ectropion, which was closely associated with the type and timing of the skin lesions, plus its complete resolution when the FDD was brought under control, would support a relationship between the 2 entities.

We believe that FDD could be classified as a seventh form of PRP, as originally suggested, and that this addition to the Griffiths classification system8 could well be added, just as the sixth type was added by the Spanish group of Miralles et al.9 The term FDD, therefore, would be substituted by the term “type 7 PRP” or “circumscribed facial PRP” analogous to the description of the fourth PRP type (circumscribed juvenile onset). These terms would refer to a PRP form that preferentially affects the face, is most often found in women, responds poorly to treatment in general, and tends to have a prolonged chronic course.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References
[1]
C.J. Ko, P. Heald, R.J. Antaya, J.L. Bolognia.
Facial discoid dermatosis.
Int J Dermatol, 49 (2010), pp. 189-192
[2]
A. Salman, B. Tekin, A. Berenjian, L. Cinel, C. Demiskesen.
Facial discoid dermatosis. A further case of a novel entity.
J Dermatol, 42 (2015), pp. 1132-1133
[3]
M. Bohdanowicz, J.G. Dekoven.
Improvement in facial discoid dermatosis with calcipotriol/betamethasone ointment and low-dose acitretin.
Clin Exp Dermatol, 43 (2018), pp. 820-821
[4]
E.Y. Gan, S.K. Ng, C.L. Goh, S.S.J. Lee.
Recalcitrant psoriasiform dermatosis of the face: is it related to pitiriasis rubra pilaris?.
J Cutan Pathol, 45 (2018), pp. 491-497
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Surgical management of cicatricial ectropión in pitiryasis rubra pilaris.
Ophtal Plast Reconstr Surg, 32 (2016), pp. e12-e15
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Resolution of pityriasis rubra pilaris-induced cicatricial ectropion with systemic low-dose methotrexate.
Am J Ophtalmol, 143 (2007), pp. 709-710
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D. Wang, V.L.C. Chong, W.S. Chong, H.H. Oon.
A review of pityriasis rubra pilaris.
Am J Clin Dermatol, 19 (2018), pp. 377-390
[9]
E.S. Miralles, M. Núñez, M.E. De Las Heras, B. Pérez, R. Moreno, A. Ledo.
Pityriasis rubra pilaris and human inmunodeficiency virus infection.
Br J Dermatol, 133 (1995), pp. 990-993
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