Midline cervical cleft: A rare anomaly

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A rare congenital midline cervical cleft.

A rare case of congenital midline cervical cleft (CMCC) is presented to highlight the importance of correct recognition of the lesion and appropriate surgical management. A 2-week-old female baby was referred to the paediatric outpatient depar tment at Red Cross War Memorial Children's Hospital with an anterior midline neck lesion that had been diagnosed at birth. She had been born by vaginal d...

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Clinical and Imaging Features of a Congenital Midline Cervical Cleft in a Neonate: A Rare Anomaly

Congenital midline cervical cleft (CMCC) is a rare congenital anomaly. CMCC and its complications and treatment have been well described in ENT, dermatology, and pediatric surgery literature. However, to our knowledge, the imaging work-up has not been reported in the literature thus far. We present a case of CMCC in a neonate with description of clinical presentation and imaging features.

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Congenital Midline Cervical Cleft

accessory components. By collapsing the unnecessary space and reconstructing a new tragus, we achieved an ideal distance from the new tragus to the auditory canal, which could not be attained by filling the hollow using cartilage graft. Because the shape and conditions of polyotia are very inconstant and the incidence of this anomaly is rare, it is difficult to establish a uniform surgical tech...

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Congenital midline cervical cleft.

Congenital midline cervical cleft is a rare anomaly that typically presents in the neonatal period as a thin suprasternal vertical band of erythematous skin with a nipple-like projection superiorly, which may exude fluid. We present the clinical and pathophysiologic features and the imaging findings of this uncommon, and rarely described entity in a newborn girl.

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Congenital Midline Cervical Cleft

On palpation, sub-mental bony spur was felt. The defect was associated with limitation of neck extension. Surgery was offered. At operation the extent of the sinus was about 4-6mm. The skin defect along with its cranial and caudal lesions was excised. The surgical wound was closed with multiple z-plasties (Fig. 2). The postoperative recovery was uneventful. Histopathology of the specimen showed...

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ژورنال

عنوان ژورنال: Anales de Pediatría (English Edition)

سال: 2019

ISSN: 2341-2879

DOI: 10.1016/j.anpede.2018.05.009