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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Fox-Fordyce disease &#40;FFD&#41;&#44; or apocrine miliaria&#44; is a rare inflammatory disease of the apocrine glands characterized by the presence of pruritic follicular papules in apocrine-rich areas of the skin&#46; We present a case of histologically confirmed FFD with extensive involvement of 2 unusual sites&#44; the chest and abdomen&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 39-year-old woman was referred for evaluation of an asymptomatic rash that had appeared 2 years earlier&#46; There was no significant personal or family medical history&#46; The rash had first appeared in the presternal area and had then spread over the abdomen to the pubic region&#46; The rash consisted of multiple minute nonconfluent red-to-yellow papules on the breasts and especially the lower chest and abdomen&#44; as far as the pubic region &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The axillae&#44; areolae&#44; and genitals were uninvolved&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Histologic examination of a papule from the lower presternal region revealed dilatation and hyperkeratotic plugging of the follicular infundibulum&#44; which was surrounded by abundant foamy histiocytes &#40;xanthomized macrophages&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#59; a mild-to-moderate periadnexal chronic lymphocytic inflammatory response&#59; and clusters of apocrine cells&#44; with a tendency to cystic dilatation&#44; between the reticular dermis and hypodermis &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">There were no relevant findings in the blood panel and the basic hormone panel&#44; which included testosterone&#44; dehydroepiandrosterone sulfate&#44; progesterone&#44; estradiol&#44; luteinizing hormone&#44; and follicle-stimulating hormone&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">No improvement was noted after successive attempts at topical treatment with tretinoin&#44; corticosteroids&#44; and clindamycin&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">FFD was first described by Fox and Fordyce in 1902&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> This rare skin condition is most common in women aged 13 to 35 years&#46; The etiology and pathogenesis of FFD are unknown&#44; although genetic&#44; endocrine&#44; environmental&#44; and metabolic factors have been proposed&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Plugging of the apocrine duct at its point of entry in the follicular infundibulum appears to be the chief factor involved in the development of FFD&#46; Plugging is thought to cause secretions to accumulate and then extravasate into the infundibulum and the peri-infundibular dermis&#44; leading to a secondary inflammatory response that largely consists of macrophage recruitment&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Clinical presentation usually includes multiple white-to-yellow follicular papules symmetrically located in characteristic regions with an abundance of apocrine glands&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Lesions are frequently pruritic and worsen in the summer months and at times of emotional stress&#46; Involved areas show little body hair growth and no sweating&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">FFD chiefly manifests in areas rich in apocrine glands&#58; the axillae&#44; mammary areolae&#44; periumbilical region&#44; mons pubis&#44; labia minora&#44; scrotum&#44; foreskin&#44; perianal region&#44; free margins of the eyelids&#44; and external ears&#46; Apocrine glands are sparsely present in all other skin regions&#44; especially the trunk and head&#44;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> but FFD has only occasionally been reported in sites other than those listed&#46; Unusual reported locations include the presternal and periumbilical regions and internal surface of the thighs&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The defining histopathologic features of FFD vary widely&#46; Descriptions include dilatation and hyperkeratosis of the follicular infundibulum&#44; spongiosis and dyskeratosis of the infundibular epithelium&#44; vacuolar degeneration of the dermoepidermal junction&#44; presence of periadnexal inflammatory lymphocytic infiltrate&#44; parakeratosis of the infundibular epithelium in the form of cornoid lamellae&#44; dilatation of the apocrine glands&#44; and perifollicular xanthomatosis&#46; The last is considered among the most characteristic findings&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;8&#44;9</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Generally speaking&#44; treatment of FFD is less than satisfactory&#44; and the condition is typically chronic&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Treatment approaches used with varying results include topical and intralesional corticosteroids&#44; topical or systemic retinoids&#44; topical antibiotics &#40;such as clindamycin&#41;&#44; oral contraceptives&#44; and topical pimecrolimus&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> Highly refractory cases have sometimes led to surgical treatment&#44; 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Case and Research Letters
Fox-Fordyce Disease With an Atypical Clinical Presentation
Enfermedad de Fox-Fordyce con presentación clínica atípica
I. Ballester
Corresponding author
ibalnor@gmail.com

Corresponding author.
, Á. López-Ávila, S. Ortiz
Servicio de Dermatología, Hospital Universitario Sta. María del Rosell de Cartagena, Murcia, Spain
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    "titulo" => "Fox-Fordyce Disease With an Atypical Clinical Presentation"
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          "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Dilatation and hyperkeratotic plugging of the follicular infundibulum surrounded by an abundance of xanthomized macrophages &#40;hematoxylin-eosin&#44; original magnification &#215;50&#41;&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Fox-Fordyce disease &#40;FFD&#41;&#44; or apocrine miliaria&#44; is a rare inflammatory disease of the apocrine glands characterized by the presence of pruritic follicular papules in apocrine-rich areas of the skin&#46; We present a case of histologically confirmed FFD with extensive involvement of 2 unusual sites&#44; the chest and abdomen&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 39-year-old woman was referred for evaluation of an asymptomatic rash that had appeared 2 years earlier&#46; There was no significant personal or family medical history&#46; The rash had first appeared in the presternal area and had then spread over the abdomen to the pubic region&#46; The rash consisted of multiple minute nonconfluent red-to-yellow papules on the breasts and especially the lower chest and abdomen&#44; as far as the pubic region &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The axillae&#44; areolae&#44; and genitals were uninvolved&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Histologic examination of a papule from the lower presternal region revealed dilatation and hyperkeratotic plugging of the follicular infundibulum&#44; which was surrounded by abundant foamy histiocytes &#40;xanthomized macrophages&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#59; a mild-to-moderate periadnexal chronic lymphocytic inflammatory response&#59; and clusters of apocrine cells&#44; with a tendency to cystic dilatation&#44; between the reticular dermis and hypodermis &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">There were no relevant findings in the blood panel and the basic hormone panel&#44; which included testosterone&#44; dehydroepiandrosterone sulfate&#44; progesterone&#44; estradiol&#44; luteinizing hormone&#44; and follicle-stimulating hormone&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">No improvement was noted after successive attempts at topical treatment with tretinoin&#44; corticosteroids&#44; and clindamycin&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">FFD was first described by Fox and Fordyce in 1902&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> This rare skin condition is most common in women aged 13 to 35 years&#46; The etiology and pathogenesis of FFD are unknown&#44; although genetic&#44; endocrine&#44; environmental&#44; and metabolic factors have been proposed&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Plugging of the apocrine duct at its point of entry in the follicular infundibulum appears to be the chief factor involved in the development of FFD&#46; Plugging is thought to cause secretions to accumulate and then extravasate into the infundibulum and the peri-infundibular dermis&#44; leading to a secondary inflammatory response that largely consists of macrophage recruitment&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Clinical presentation usually includes multiple white-to-yellow follicular papules symmetrically located in characteristic regions with an abundance of apocrine glands&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Lesions are frequently pruritic and worsen in the summer months and at times of emotional stress&#46; Involved areas show little body hair growth and no sweating&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">FFD chiefly manifests in areas rich in apocrine glands&#58; the axillae&#44; mammary areolae&#44; periumbilical region&#44; mons pubis&#44; labia minora&#44; scrotum&#44; foreskin&#44; perianal region&#44; free margins of the eyelids&#44; and external ears&#46; Apocrine glands are sparsely present in all other skin regions&#44; especially the trunk and head&#44;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> but FFD has only occasionally been reported in sites other than those listed&#46; Unusual reported locations include the presternal and periumbilical regions and internal surface of the thighs&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The defining histopathologic features of FFD vary widely&#46; Descriptions include dilatation and hyperkeratosis of the follicular infundibulum&#44; spongiosis and dyskeratosis of the infundibular epithelium&#44; vacuolar degeneration of the dermoepidermal junction&#44; presence of periadnexal inflammatory lymphocytic infiltrate&#44; parakeratosis of the infundibular epithelium in the form of cornoid lamellae&#44; dilatation of the apocrine glands&#44; and perifollicular xanthomatosis&#46; The last is considered among the most characteristic findings&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;8&#44;9</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Generally speaking&#44; treatment of FFD is less than satisfactory&#44; and the condition is typically chronic&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Treatment approaches used with varying results include topical and intralesional corticosteroids&#44; topical or systemic retinoids&#44; topical antibiotics &#40;such as clindamycin&#41;&#44; oral contraceptives&#44; and topical pimecrolimus&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> Highly refractory cases have sometimes led to surgical treatment&#44; including electrocoagulation&#44; excision&#44; and liposuction&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">In conclusion&#44; we believe that FFD should be considered in the differential diagnosis of any progressive rash of red-to-yellow papules on the chest or abdomen&#46; Clinically similar&#44; easily confused conditions more frequently described at these sites include syringomas&#44; steatocystoma multiplex&#44; or lichen nitidus&#44; and distinguishing them from FFD requires the correlation of both clinical and histologic findings&#46;</p></span>"
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Article information
ISSN: 15782190
Original language: English
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Idiomas
Actas Dermo-Sifiliográficas
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