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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Follicular mucinosis is a rare condition&#44; belonging to the group of cutaneous mucinoses&#44; characterized by localized or diffuse mucin deposits in the skin or within hair follicles&#46; Two forms were described&#58; primary &#40;or idiopathic&#41; and secondary form&#44; which may be associated with benign or malignant conditions&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The presence of well-defined papular&#44; erythematous or reddish-brown erythema papules or plaques clinically characterize the condition&#46; Follicular keratosis or alopecic patches could also be observed&#46; Other less common forms have been described&#44; such as acneiform&#44; eczematous&#44; cystic or nodular&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient is an 11-year-old white male&#44; with no relevant personal or family history&#44; with a 2 year history of asymptomatic cutaneous lesion on the face&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">On the dermatological examination&#58; hypochromic lesion topped by follicular and nonfollicular shiny papules on the nasal&#44; malar&#44; zygomatic and left periorbital region and papular lesions on the upper right eyelid and mild left eyelid edema &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Sensory evaluation results are normal&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">A routine anatomopathological examination &#40;Hematoxylin &#38; eosin staining&#41; reveals preserved epidermis&#46; Dermis presents some hair follicles containing fibromyxoid stroma and mixed pattern inflammatory cells &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Alcian Blue stain reveals built-up mucin in the outer root sheath of the hair follicle &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">Laboratory tests were requested to investigate associated diseases&#59; all results were normal&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Treatment with daily application of high-potency topical corticosteroid showed improvement&#59; however&#44; recurrence occurred when discontinued&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">In 1957&#44; Hermann Pinkus described a group of 6 patients with localized alopecia&#44; histopathologically characterized by mucin deposits in the hair follicles&#44; which he named alopecia mucinosa&#46; Jablonska et al&#46; proposed in 1959 to change the name to follicular mucinosis&#44; a term accepted to this day&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Its cause is still unknown&#46; Today&#44; it is considered a standard reaction of the follicular epithelium to various factors&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">This dermatosis can have two clinical forms&#58;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">1&#44;2&#44;4</span></a><ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">1&#46;</span><p id="par0055" class="elsevierStylePara elsevierViewall">Primary form&#58; an idiopathic&#44; benign and transient form&#44; which commonly occurs in children and adults&#46; In younger patients&#44; it usually affects the head and neck&#44; receding spontaneously after 2&#8211;24 months in most cases&#46; Some rare cases of developing Hodgkin&#39;s disease&#44; other lymphomas and leukemia have been recorded&#46; Adult patients present generalized lesions that may last indefinitely&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">2&#46;</span><p id="par0060" class="elsevierStylePara elsevierViewall">Secondary form&#58; normally affects adults and older patients&#44; and is associated with an underlying inflammatory or neoplastic condition&#46; The most common is mycosis fungoides&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p></li></ul></p><p id="par0065" class="elsevierStylePara elsevierViewall">In the reported case&#44; clinical and lab analysis allowed to exclude associated diseases and diagnose the condition as the idiopathic form of follicular mucinosis&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">Histopathology is essential for diagnosis since it shows mucin deposits on the outer root sheath of the hair follicle&#44; in addition to inflammatory infiltrates composed of lymphocytes&#44; macrophages and eosinophils with folliculotropic lymphocytes&#46; The benign form is determined by the extension of the eosinophilic inflammatory infiltrate and significant mucinous alterations in the follicular epithelium&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Similar findings were observed in the patient&#8216;s results&#46; Presence of epidermotropic lymphocytes and dense perifollicular infiltrate of atypical cells suggest a malignant form of the condition&#59; however&#44; no evidence of it was found in the studied patient&#46;</p><p id="par0075" class="elsevierStylePara elsevierViewall">It&#39;s interesting to mention that the chances of lymphomas appearing in follicular mucinosis patients varies greatly&#46; The criteria adopted in the different evaluations change ranging from 14&#37; to 32&#37;&#46; For example&#44; Coskey and Mehregan detected lymphoma in 7 out of 50 follicular mucinosis patients &#40;14&#37;&#41;&#44; Emmerson in 8 out of 47 patients &#40;17&#37;&#41;&#44; Logan and Headington in 21 out of 80 patients &#40;26&#37;&#41;&#44; Mehregan et al&#46; in 9 out of 33 patients &#40;27&#46;2&#37;&#41; and Gibson et al&#46; in 19 out of 59 patients &#40;32&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">On the other hand&#44; the frequency of the disease among patients with cutaneous lymphomas has not been established in literature&#46; Marti et al&#46; found the disease in 5 out of 43 patients &#40;11&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0085" class="elsevierStylePara elsevierViewall">Regarding treatment&#44; there is no specific medication for idiopathic follicular mucinosis&#46; However&#44; topical&#44; intralesional and systemic corticosteroids&#44; in addition to dapsone&#44; antimalarial&#44; isotretinoin and minocycline&#44; can be used&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> Treatment was done using topical corticosteroids&#59; the lesions improved but had a slight recurrence&#46; These patients require periodic monitoring&#46;</p><p id="par0090" class="elsevierStylePara elsevierViewall">The importance of the report is that is shows a rare incidence of follicular mucinosis in childhood&#46; It is imperative to emphasize the obligation of long-term monitoring in order to completely rule out the connection with associated neoplasias&#46;</p><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Financial support</span><p id="par0115" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Authors&#8217; contributions</span><p id="par0095" class="elsevierStylePara elsevierViewall">Fernanda Jos&#233; Bauer&#58; Conception and planning of the study&#59; elaboration and writing of the manuscript&#59; obtaining&#44; analysis&#44; and interpretation of the data&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p><p id="par0100" class="elsevierStylePara elsevierViewall">Jos&#233; Roberto Paes de Almeida&#58; Approval of the final version of the manuscript&#59; conception and planning of the study&#59; effective participation in research orientation&#59; intellectual participation in the propaedeutic and&#47;or therapeutic conduct of the studied cases&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p><p id="par0105" class="elsevierStylePara elsevierViewall">Angelo Sementilli&#58; Obtaining&#44; analysis&#44; and interpretation of the data&#46;</p><p id="par0110" class="elsevierStylePara elsevierViewall">Sandra Lopes Mattos e Dinato&#58; Approval of the final version of the manuscript&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0120" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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Case Letter
Idiopathic follicular mucinosis in childhood
Fernanda José Bauer
Autor para correspondência
fer_bauer_90@hotmail.com

Corresponding author.
, José Roberto Paes de Almeida, Angelo Sementilli, Sandra Lopes Mattos e Dinato
Department of Dermatology, Centro Universitário Lusíada, Santos, SP, Brazil
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Follicular mucinosis is a rare condition&#44; belonging to the group of cutaneous mucinoses&#44; characterized by localized or diffuse mucin deposits in the skin or within hair follicles&#46; Two forms were described&#58; primary &#40;or idiopathic&#41; and secondary form&#44; which may be associated with benign or malignant conditions&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The presence of well-defined papular&#44; erythematous or reddish-brown erythema papules or plaques clinically characterize the condition&#46; Follicular keratosis or alopecic patches could also be observed&#46; Other less common forms have been described&#44; such as acneiform&#44; eczematous&#44; cystic or nodular&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient is an 11-year-old white male&#44; with no relevant personal or family history&#44; with a 2 year history of asymptomatic cutaneous lesion on the face&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">On the dermatological examination&#58; hypochromic lesion topped by follicular and nonfollicular shiny papules on the nasal&#44; malar&#44; zygomatic and left periorbital region and papular lesions on the upper right eyelid and mild left eyelid edema &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Sensory evaluation results are normal&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">A routine anatomopathological examination &#40;Hematoxylin &#38; eosin staining&#41; reveals preserved epidermis&#46; Dermis presents some hair follicles containing fibromyxoid stroma and mixed pattern inflammatory cells &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Alcian Blue stain reveals built-up mucin in the outer root sheath of the hair follicle &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">Laboratory tests were requested to investigate associated diseases&#59; all results were normal&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Treatment with daily application of high-potency topical corticosteroid showed improvement&#59; however&#44; recurrence occurred when discontinued&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">In 1957&#44; Hermann Pinkus described a group of 6 patients with localized alopecia&#44; histopathologically characterized by mucin deposits in the hair follicles&#44; which he named alopecia mucinosa&#46; Jablonska et al&#46; proposed in 1959 to change the name to follicular mucinosis&#44; a term accepted to this day&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Its cause is still unknown&#46; Today&#44; it is considered a standard reaction of the follicular epithelium to various factors&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">This dermatosis can have two clinical forms&#58;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">1&#44;2&#44;4</span></a><ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">1&#46;</span><p id="par0055" class="elsevierStylePara elsevierViewall">Primary form&#58; an idiopathic&#44; benign and transient form&#44; which commonly occurs in children and adults&#46; In younger patients&#44; it usually affects the head and neck&#44; receding spontaneously after 2&#8211;24 months in most cases&#46; Some rare cases of developing Hodgkin&#39;s disease&#44; other lymphomas and leukemia have been recorded&#46; Adult patients present generalized lesions that may last indefinitely&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">2&#46;</span><p id="par0060" class="elsevierStylePara elsevierViewall">Secondary form&#58; normally affects adults and older patients&#44; and is associated with an underlying inflammatory or neoplastic condition&#46; The most common is mycosis fungoides&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p></li></ul></p><p id="par0065" class="elsevierStylePara elsevierViewall">In the reported case&#44; clinical and lab analysis allowed to exclude associated diseases and diagnose the condition as the idiopathic form of follicular mucinosis&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">Histopathology is essential for diagnosis since it shows mucin deposits on the outer root sheath of the hair follicle&#44; in addition to inflammatory infiltrates composed of lymphocytes&#44; macrophages and eosinophils with folliculotropic lymphocytes&#46; The benign form is determined by the extension of the eosinophilic inflammatory infiltrate and significant mucinous alterations in the follicular epithelium&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Similar findings were observed in the patient&#8216;s results&#46; Presence of epidermotropic lymphocytes and dense perifollicular infiltrate of atypical cells suggest a malignant form of the condition&#59; however&#44; no evidence of it was found in the studied patient&#46;</p><p id="par0075" class="elsevierStylePara elsevierViewall">It&#39;s interesting to mention that the chances of lymphomas appearing in follicular mucinosis patients varies greatly&#46; The criteria adopted in the different evaluations change ranging from 14&#37; to 32&#37;&#46; For example&#44; Coskey and Mehregan detected lymphoma in 7 out of 50 follicular mucinosis patients &#40;14&#37;&#41;&#44; Emmerson in 8 out of 47 patients &#40;17&#37;&#41;&#44; Logan and Headington in 21 out of 80 patients &#40;26&#37;&#41;&#44; Mehregan et al&#46; in 9 out of 33 patients &#40;27&#46;2&#37;&#41; and Gibson et al&#46; in 19 out of 59 patients &#40;32&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">On the other hand&#44; the frequency of the disease among patients with cutaneous lymphomas has not been established in literature&#46; Marti et al&#46; found the disease in 5 out of 43 patients &#40;11&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0085" class="elsevierStylePara elsevierViewall">Regarding treatment&#44; there is no specific medication for idiopathic follicular mucinosis&#46; However&#44; topical&#44; intralesional and systemic corticosteroids&#44; in addition to dapsone&#44; antimalarial&#44; isotretinoin and minocycline&#44; can be used&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> Treatment was done using topical corticosteroids&#59; the lesions improved but had a slight recurrence&#46; These patients require periodic monitoring&#46;</p><p id="par0090" class="elsevierStylePara elsevierViewall">The importance of the report is that is shows a rare incidence of follicular mucinosis in childhood&#46; It is imperative to emphasize the obligation of long-term monitoring in order to completely rule out the connection with associated neoplasias&#46;</p><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Financial support</span><p id="par0115" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Authors&#8217; contributions</span><p id="par0095" class="elsevierStylePara elsevierViewall">Fernanda Jos&#233; Bauer&#58; Conception and planning of the study&#59; elaboration and writing of the manuscript&#59; obtaining&#44; analysis&#44; and interpretation of the data&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p><p id="par0100" class="elsevierStylePara elsevierViewall">Jos&#233; Roberto Paes de Almeida&#58; Approval of the final version of the manuscript&#59; conception and planning of the study&#59; effective participation in research orientation&#59; intellectual participation in the propaedeutic and&#47;or therapeutic conduct of the studied cases&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p><p id="par0105" class="elsevierStylePara elsevierViewall">Angelo Sementilli&#58; Obtaining&#44; analysis&#44; and interpretation of the data&#46;</p><p id="par0110" class="elsevierStylePara elsevierViewall">Sandra Lopes Mattos e Dinato&#58; Approval of the final version of the manuscript&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0120" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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