Aplasia cutis congenita of the scalp with sagittal venous sinus exposure

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Aplasia Cutis Congenita of the Scalp

Dr. João Paulo Cavalcante de Almeida – Rua Paulo Morais 130 60175-175 Fortaleza CE Brasil. E-mail: [email protected] Aplasia cutis congenita (ACC) is an uncommon disorder that presents as a focal defect of the skin at birth, frequently involving the midline over the skull vertex (70%), but it may affect any region of the body. Since 1767, about 500 cases have been reported in medica...

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Aplasia cutis congenita of the scalp.

Aplasia cutis congenita is the congenital absence of skin. The majority of these defects involve the vertex of the scalp in the area overlying the sagittal sinus. The larger defects are predisposed to sudden lethal hemorrhage and require urgent closure. Local rotational scalp flaps are recommended for closure of the larger defects because they provide the most reliable coverage, eliminate the r...

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Aplasia Cutis Congenita of the Scalp with a Familial Pattern: A Case Report

Aplasia Cutis Conginita (ACC) is a condition characterized by congenital absence of skin, usually on the scalp. ACC can occur as an isolated condition or in the presence of other congenital anomalies. Here we describe a case of a 16 days old baby girl with an isolated ACC of the scalp. Her elder two siblings have been diagnosed with ACC with concomitant cardiac or limb anomalies. The patient wa...

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Aplasia cutis congenita

The patient was a female neonate bornprematurely at 36 weeks of gestation by a Cesareansection. During pregnancy, the mother had nohistory of fever, drug use, or X-ray exposure.The mother was gravida 2 and had no history ofabortion. Her first child was healthy. There wasno record of birth trauma. The perinatal historywas negative for intrauterine trauma, the use ofantithyroid medication, or mis...

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[Hair collar sign associated with scalp aplasia cutis congenita].

1. Méndez T, Otero I, García R, Pérez B. Síndrome de Klippel-Trenaunay-Weber: presentación de un caso. Rev Cubana Oftalmol. 2001;14:47-9. 2. Bordel MT, Miranda A. Un caso atípico de síndrome de Klippel-Trenaunay. Piel. 2005;20:306-8. 3. Gimeno P, Pérez P, López-Pisón J, Romeo M, Galeano N, Marco M, et al. Síndrome de Klippel-Trenaunay: a propósito de tres nuevas observaciones. An Esp Pediatr. 2...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood - Fetal and Neonatal Edition

سال: 2016

ISSN: 1359-2998,1468-2052

DOI: 10.1136/archdischild-2016-310480