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measuring 3 to 15<span class="elsevierStyleHsp" style=""></span>cm in diameter &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The patient stated that the lesions had first appeared on her chest and that they had gradually increased in size and number&#44; spreading to the abdomen&#44; buttocks&#44; and upper and lower limbs&#46; She reported no associated symptoms or previous treatment&#46; Histopathology revealed hyperkeratosis&#44; parakeratosis&#44; a reduction in the granular layer&#44; increased pigmentation of the basal keratinocytes&#44; loss of the crest pattern&#44; and a mild superficial perivascular lymphocytic infiltrate &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The findings were consistent with a diagnosis of PR&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Laboratory tests including complete blood count&#44; biochemistry&#44; urinalysis&#44; Mantoux test&#44; and tumor markers &#40;&#945;-fetoprotein&#44; Ca 19&#46;9&#44; Ca 125&#44; &#946;<span class="elsevierStyleInf">2</span>-microglobulin&#44; and carcinoembryonic antigen&#41; were normal or negative&#46; Computed tomography of the chest&#44; abdomen&#44; and pelvis&#44; upper gastrointestinal endoscopy&#44; and colonoscopy were normal&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">After making the diagnosis&#44; treatment was started with 10&#37; salicylic acid cream and a combination of betamethasone plus calcipotriol&#44; which led to a partial response&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">PR&#44; a rare disorder of keratinization&#44; was described by Toyoma in 1906 as pityriasis circinata&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">2</span></a> The frequency in the American continent is unknown&#44; but it is considered a common disease in Japan&#44; western India&#44; and South Africa&#44; where the prevalence is of 63 cases per 5800 population&#46; PR affects men and women equally and is most common between the ages of 20 and 45 years&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">3</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The etiology is unknown&#44; though the majority of authors believe PR to be an acquired form of ichthyosis&#44; a late presentation of congenital ichthyosis&#44; or a cutaneous manifestation of systemic diseases such as malnutrition&#44; tuberculosis&#44; cirrhosis&#44; or tumors&#46; It has also been associated with leprosy&#44; lung and liver diseases&#44; multiple myeloma&#44; chronic myeloid leukemia&#44; heart disease&#44; and diabetes&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">4&#44;5</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Concerning the pathogenesis of PR&#44; Makino et al&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">6</span></a> recently described a reduction or absence of expression of filaggrin 2 in the epidermis of PR lesions&#44; similar to the findings in lesions of atopic dermatitis&#44; ichthyosis vulgaris&#44; and psoriasis vulgaris&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Clinically&#44; PR is characterized by the appearance of very well-defined&#44; hyper- or hypopigmented circular plaques of ichthyosiform appearance&#44; with no associated inflammatory signs&#46; Lesions occur on the back&#44; upper and lower limbs&#44; abdomen&#44; and buttocks&#59; their number can vary between 1 and 100&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a> and they can persist for months to years&#44; with exacerbations during the winter&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Various changes can be seen on histopathology&#44; including hyperkeratosis&#44; flattening of the epidermal crests&#44; a reduction or absence of the granular layer&#44; hyperpigmentation of basal layer&#44; mild spongiosis&#44; comedo-like openings&#44; incontinentia pigmenti&#44; and a superficial perivascular infiltrate&#59; the histopathological appearance may even be normal in some cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">1&#44;4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Two subtypes have been proposed&#46; Type 1&#44; common in African American and Asian individuals&#44; is characterized by a small number of hyperpigmented lesions in patients with no family history of the disease and it is associated with malignant and systemic diseases&#46; Type 2&#44; which&#44; in contrast&#44; is more common in white patients with a family history of the disease&#44; presents more numerous&#44; hypopigmented plaques and is not associated with malignant diseases&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">7</span></a> Despite this classification&#44; some reported cases show characteristics of both subtypes&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">4</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis includes tinea versicolor&#44; tinea corporis&#44; nummular eczema&#44; fixed drug reaction&#44; erythrasma&#44; pityriasis rosea&#44; figurate erythema&#44; and leprosy&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Treatment is difficult in most cases&#46; Topical corticosteroids&#44; antifungal agents&#44; salicylic acid&#44; topical and oral retinoids&#44; lactic acid lotions&#44; and tars have been used without success&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">1&#44;4</span></a> Recently&#44; treatment with vitamin D3 has produced a gradual improvement in the lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">6</span></a> When an underlying disease is present&#44; its treatment can lead to improvement or even resolution of the PR lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">8</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">To our knowledge&#44; this is the first reported case of PR associated with hyperprolactinemia&#44; and we therefore consider its publication important&#46; The finding of this dermatosis should always alert the physician to the possibility of malignancy&#44; systemic diseases&#44; or hormonal disorders&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case and Research Letters
Pityriasis Rotunda and Hyperprolactinemia
Pitiriasis rotunda e hiperprolactinemia
V. Pinos-Leóna,b,
Autor para correspondencia
, M. Núñeza,b, M. Salazara,b, V. Solís-Bowena,b
a Servicio de Dermatología, Hospital San Francisco de Quito, Instituto Ecuatoriano de Seguridad Social, Quito, Ecuador
b Universidad Central del Ecuador, Quito, Ecuador
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Pityriasis rotunda &#40;PR&#41; is a rare acquired disease of keratinization&#46; It presents as well-defined&#44; scaly round plaques that can be hyper- or hypopigmented&#46; PR mainly affects young adults of African descent and shows no gender preference&#46; It has been associated with systemic diseases and malignant tumors&#44; though many cases present no associated disorders&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a> We present a case of intense PR associated with hyperprolactinemia&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The patient was a 38-year-old African American woman with a history of hyperprolactinemia on treatment with cabergoline for the previous 7 months&#46; She attended dermatology outpatients for a 9-month history of sharply outlined&#44; circumscribed hyperpigmented plaques of ichthyosiform appearance&#44; measuring 3 to 15<span class="elsevierStyleHsp" style=""></span>cm in diameter &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The patient stated that the lesions had first appeared on her chest and that they had gradually increased in size and number&#44; spreading to the abdomen&#44; buttocks&#44; and upper and lower limbs&#46; She reported no associated symptoms or previous treatment&#46; Histopathology revealed hyperkeratosis&#44; parakeratosis&#44; a reduction in the granular layer&#44; increased pigmentation of the basal keratinocytes&#44; loss of the crest pattern&#44; and a mild superficial perivascular lymphocytic infiltrate &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The findings were consistent with a diagnosis of PR&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Laboratory tests including complete blood count&#44; biochemistry&#44; urinalysis&#44; Mantoux test&#44; and tumor markers &#40;&#945;-fetoprotein&#44; Ca 19&#46;9&#44; Ca 125&#44; &#946;<span class="elsevierStyleInf">2</span>-microglobulin&#44; and carcinoembryonic antigen&#41; were normal or negative&#46; Computed tomography of the chest&#44; abdomen&#44; and pelvis&#44; upper gastrointestinal endoscopy&#44; and colonoscopy were normal&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">After making the diagnosis&#44; treatment was started with 10&#37; salicylic acid cream and a combination of betamethasone plus calcipotriol&#44; which led to a partial response&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">PR&#44; a rare disorder of keratinization&#44; was described by Toyoma in 1906 as pityriasis circinata&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">2</span></a> The frequency in the American continent is unknown&#44; but it is considered a common disease in Japan&#44; western India&#44; and South Africa&#44; where the prevalence is of 63 cases per 5800 population&#46; PR affects men and women equally and is most common between the ages of 20 and 45 years&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">3</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The etiology is unknown&#44; though the majority of authors believe PR to be an acquired form of ichthyosis&#44; a late presentation of congenital ichthyosis&#44; or a cutaneous manifestation of systemic diseases such as malnutrition&#44; tuberculosis&#44; cirrhosis&#44; or tumors&#46; It has also been associated with leprosy&#44; lung and liver diseases&#44; multiple myeloma&#44; chronic myeloid leukemia&#44; heart disease&#44; and diabetes&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">4&#44;5</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Concerning the pathogenesis of PR&#44; Makino et al&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">6</span></a> recently described a reduction or absence of expression of filaggrin 2 in the epidermis of PR lesions&#44; similar to the findings in lesions of atopic dermatitis&#44; ichthyosis vulgaris&#44; and psoriasis vulgaris&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Clinically&#44; PR is characterized by the appearance of very well-defined&#44; hyper- or hypopigmented circular plaques of ichthyosiform appearance&#44; with no associated inflammatory signs&#46; Lesions occur on the back&#44; upper and lower limbs&#44; abdomen&#44; and buttocks&#59; their number can vary between 1 and 100&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a> and they can persist for months to years&#44; with exacerbations during the winter&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Various changes can be seen on histopathology&#44; including hyperkeratosis&#44; flattening of the epidermal crests&#44; a reduction or absence of the granular layer&#44; hyperpigmentation of basal layer&#44; mild spongiosis&#44; comedo-like openings&#44; incontinentia pigmenti&#44; and a superficial perivascular infiltrate&#59; the histopathological appearance may even be normal in some cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">1&#44;4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Two subtypes have been proposed&#46; Type 1&#44; common in African American and Asian individuals&#44; is characterized by a small number of hyperpigmented lesions in patients with no family history of the disease and it is associated with malignant and systemic diseases&#46; Type 2&#44; which&#44; in contrast&#44; is more common in white patients with a family history of the disease&#44; presents more numerous&#44; hypopigmented plaques and is not associated with malignant diseases&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">7</span></a> Despite this classification&#44; some reported cases show characteristics of both subtypes&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">4</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis includes tinea versicolor&#44; tinea corporis&#44; nummular eczema&#44; fixed drug reaction&#44; erythrasma&#44; pityriasis rosea&#44; figurate erythema&#44; and leprosy&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Treatment is difficult in most cases&#46; Topical corticosteroids&#44; antifungal agents&#44; salicylic acid&#44; topical and oral retinoids&#44; lactic acid lotions&#44; and tars have been used without success&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">1&#44;4</span></a> Recently&#44; treatment with vitamin D3 has produced a gradual improvement in the lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">6</span></a> When an underlying disease is present&#44; 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