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1</a>&#41;&#46; The lesion was not adhered to deeper tissues and showed no mobility when the patient swallowed or moved his tongue&#46; A catheter was inserted into the orifice and reached a dead end after penetrating about 3-4<span class="elsevierStyleHsp" style=""></span>mm&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Additional Tests</span><p id="par0015" class="elsevierStylePara elsevierViewall">Dermoscopic examination revealed a pink pedunculated papule measuring 0&#46;3<span class="elsevierStyleHsp" style=""></span>cm in diameter&#44; at the inferior end of which was a fissure &#40;barely visible to the naked eye&#41; measuring 0&#46;1<span class="elsevierStyleHsp" style=""></span>cm with a mild transparent exudate &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Soft-tissue ultrasound examination revealed a round&#44; well-defined hypoechoic superficial lesion that showed no evidence of a fistulous tract as well as a thyroid with a typical morphology and location&#46; Complete blood count&#44; biochemistry&#44; and hormone panel were normal&#46; An electrocardiogram &#40;ECG&#41; was carried out as a first step to rule out cardiac abnormalities&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Midline cervical cleft &#40;MCC&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course</span><p id="par0035" class="elsevierStylePara elsevierViewall">The patient was assessed by the pediatric surgery department and an initial attitude of watchful waiting was adopted&#46; 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but there have been cases in which it extends to the subcutaneous tissue and underlying muscle&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> The size of the lesion can be highly variable and it can be located anywhere along the anterior midline from the lower lip to the suprasternal region&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> The condition is generally detected at birth&#44; but mild forms can go undetected or can be mistaken for remnants of the thyroglossal duct or branchial anomalies&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> The differential diagnosis should include fistulas&#44; sinus cysts of branchial origin&#44; and bronchogenic cysts&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2</span></a> Branchial disease typically appears in the region anterior to the sternocleidomastoid muscle&#44; and bronchogenic cysts tend to be located in the suprasternal notch&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;4</span></a> In case of doubt&#44; ultrasound and computed tomography can be very useful in establishing a diagnosis&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The embryopathogenesis of MCC is not yet fully understood&#44; and most authors consider it to be a mild form on the spectrum of congenital branchial anomalies&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2&#44;5</span></a> This would explain the occasional association of MCC with other anomalies such as thyroglossal duct cysts&#44; dermoid cysts&#44; bronchogenic cysts&#44; cleft lip&#44; and congenital cardiac anomalies&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;6</span></a> A full hormone panel and an ECG are also recommended as a first step to rule out associated comorbidities&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">The clinical course of MCC is benign with spontaneous scarring and the formation of a fibrous cord&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;5&#44;6</span></a> However&#44; because there is considerable risk of infection&#44; cervical contracture&#44; and limitation of mobility&#44; MCC should be managed with surgery around the age of 1 year and no later than 2 years&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> The preferred technique is complete excision followed by Z-plasty closure<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#8211;6</span></a> to prevent the recurrence of fibrosis&#44; which can occur following direct closure&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a> Finally&#44; periodic follow-up of the patient throughout infancy is recommended because of the risk of retraction and hypertrophic scarring&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#44;6</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">In conclusion&#44; we have described a case of mild <span class="elsevierStyleGrantSponsor" id="gs1">MCC</span> in which the typical atrophic plaque was not evident and the diagnosis was supported by physical examination&#44; dermoscopy&#44; and ultrasound&#46; Other congenital anomalies are rarely associated with <span class="elsevierStyleGrantSponsor" id="gs2">MCC</span> and should be ruled out during the diagnostic process&#46; Treatment of the condition should be mainly surgical&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0060" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case for Diagnosis
Pedunculated Papule and Fissure in the Anterior Midline of the Neck
Pápula pediculada y fisura en línea cervical anterior de recién nacido
C. Arjona-Aguileraa,
Autor para correspondencia
cintiaarjona@hotmail.com

Corresponding author.
, G. Blasco-Morenteb, J. Tercedor-Sánchezb
a Unidad de Gestión Clínica de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario Puerta del Mar, Cádiz, Spain
b Unidad de Gestión Clínica de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario Virgen de las Nieves, Granada, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 3-month-old boy was seen for an exudative lesion in the anterior cervical region that had been present since birth&#46; The gestation period had been normal and the child had been born at full term&#46; The patient had no other medical or surgical history of interest&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed a skin-colored pedunculated papule on the anterior midline of the neck&#46; At the caudal end of the lesion&#44; there was an orifice that connected to a small mucosal fistula measuring barely 2<span class="elsevierStyleHsp" style=""></span>mm in length &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The lesion was not adhered to deeper tissues and showed no mobility when the patient swallowed or moved his tongue&#46; A catheter was inserted into the orifice and reached a dead end after penetrating about 3-4<span class="elsevierStyleHsp" style=""></span>mm&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Additional Tests</span><p id="par0015" class="elsevierStylePara elsevierViewall">Dermoscopic examination revealed a pink pedunculated papule measuring 0&#46;3<span class="elsevierStyleHsp" style=""></span>cm in diameter&#44; at the inferior end of which was a fissure &#40;barely visible to the naked eye&#41; measuring 0&#46;1<span class="elsevierStyleHsp" style=""></span>cm with a mild transparent exudate &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Soft-tissue ultrasound examination revealed a round&#44; well-defined hypoechoic superficial lesion that showed no evidence of a fistulous tract as well as a thyroid with a typical morphology and location&#46; Complete blood count&#44; biochemistry&#44; and hormone panel were normal&#46; An electrocardiogram &#40;ECG&#41; was carried out as a first step to rule out cardiac abnormalities&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Midline cervical cleft &#40;MCC&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course</span><p id="par0035" class="elsevierStylePara elsevierViewall">The patient was assessed by the pediatric surgery department and an initial attitude of watchful waiting was adopted&#46; Curative surgical treatment will be scheduled for when the boy is around 1 year of age&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">MCC is a rare congenital anomaly that causes a visible defect at the midline of the neck&#46; Around 200 cases have been described in the international literature&#44;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> mostly in plastic surgery or otorhinolaryngology journals&#46; MCC appears sporadically and is slightly more common in girls&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2</span></a> The clinical presentation is characterized by a linear vertical deepithelized plaque with a fibroepithelial papule at the cranial end that extends towards the caudal end&#44; terminating in a blind sinus&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2</span></a> The entity has no relationship to the thyroid or to the hyoid bone&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">3</span></a> The lesion is generally limited to the skin&#44; but there have been cases in which it extends to the subcutaneous tissue and underlying muscle&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> The size of the lesion can be highly variable and it can be located anywhere along the anterior midline from the lower lip to the suprasternal region&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> The condition is generally detected at birth&#44; but mild forms can go undetected or can be mistaken for remnants of the thyroglossal duct or branchial anomalies&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> The differential diagnosis should include fistulas&#44; sinus cysts of branchial origin&#44; and bronchogenic cysts&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2</span></a> Branchial disease typically appears in the region anterior to the sternocleidomastoid muscle&#44; and bronchogenic cysts tend to be located in the suprasternal notch&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;4</span></a> In case of doubt&#44; ultrasound and computed tomography can be very useful in establishing a diagnosis&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The embryopathogenesis of MCC is not yet fully understood&#44; and most authors consider it to be a mild form on the spectrum of congenital branchial anomalies&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2&#44;5</span></a> This would explain the occasional association of MCC with other anomalies such as thyroglossal duct cysts&#44; dermoid cysts&#44; bronchogenic cysts&#44; cleft lip&#44; and congenital cardiac anomalies&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;6</span></a> A full hormone panel and an ECG are also recommended as a first step to rule out associated comorbidities&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">The clinical course of MCC is benign with spontaneous scarring and the formation of a fibrous cord&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;5&#44;6</span></a> However&#44; because there is considerable risk of infection&#44; cervical contracture&#44; and limitation of mobility&#44; MCC should be managed with surgery around the age of 1 year and no later than 2 years&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> The preferred technique is complete excision followed by Z-plasty closure<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#8211;6</span></a> to prevent the recurrence of fibrosis&#44; which can occur following direct closure&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a> Finally&#44; periodic follow-up of the patient throughout infancy is recommended because of the risk of retraction and hypertrophic scarring&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#44;6</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">In conclusion&#44; we have described a case of mild <span class="elsevierStyleGrantSponsor" id="gs1">MCC</span> in which the typical atrophic plaque was not evident and the diagnosis was supported by physical examination&#44; dermoscopy&#44; and ultrasound&#46; Other congenital anomalies are rarely associated with <span class="elsevierStyleGrantSponsor" id="gs2">MCC</span> and should be ruled out during the diagnostic process&#46; Treatment of the condition should be mainly surgical&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0060" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Información del artículo
ISSN: 15782190
Idioma original: Inglés
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