- Case report
- Open Access
- Open Peer Review
Congenital midline cervical cleft: a case report
© The Author(s). 2019
- Received: 9 April 2018
- Accepted: 6 May 2019
- Published: 9 June 2019
Midline cervical cleft is a very rare congenital anomaly. According to a literature search, until 2014 only 205 cases were reported.
We present a classic case of congenital midline cervical cleft. This was a case of a 3-year-old Middle Eastern boy. The lesion was excised and the defect was closed via multiple Z-plasties.
Midline cervical cleft, although a rarity, when presented needs surgical treatment, which comprises surgical excision and closure that lessens the possibility of scar visibility and contracture.
- Midline cleft
- Congenital midline cervical cleft
- Surgical excision
- Congenital neck lesions
Midline cervical cleft (MCC) is a rare congenital anomaly. According to a literature search, by 2014 only 205 cases had been reported . The first recorded case of MCC was in 1848 by Luschka, while Bailey documented the first description of this abnormality in 1924 [2, 3]. It is an entirely sporadic lesion that is only occasionally associated with other developmental defects including bifid mandible and microgenia, clefting of the sternum, and a possible loss of other midline structures, such as portions of the hyoid bone [4, 5].
The clefts have a remarkably consistent appearance and are typically noticed at birth as a defect at the ventral aspect of the neck. Superiorly, there is a skin tag with the inferior margin being formed by a short sinus, normally approximately 1 cm in length. A mucosal surface divides the two. No antenatal problems are generally identified and Caucasian women seem to be the most frequently affected .
MCC is diagnosed by clinical examination, and the main characteristic is a protruding lesion at the midline of the anterior region of the neck, between the chin and the suprasternal notch . The cardinal diagnostic features are: (a) fistula opening is located caudally, (b) intermittent serous fluid discharge in the early neonatal period, (c) nipple-like appearance of the cleft in the superior aspect, and (d) widened scar and minimal neck contracture in later life .
Treatment is surgical excision, which is required largely to improve the cosmetic appearance of the neck and to avoid contracture formation of the ventral neck [8, 9]. We present a classic case of MCC treated with excision and defect closure via multiple Z-plasties.
The MCC consists of epidermis, a mucosal surface skeletal muscle (that is superficial to platysma), and glandular tissue. There have been many theories that attempt to explain these findings. Some propose that pressure from the pericardial roof on the developing branchial arches results in pressure necrosis and scarring. Others postulate that rupture of a pathological adhesion between the epithelium of the cardiohepatic fold with that of the ventral part of the first branchial arch causes tissue ischemia, again with localized necrosis and scarring. These theories, however, do not explain the consistent anatomy of the MCC or the presence of skeletal muscle and glandular tissue .
Another hypothesis that does help to explain the histological findings is the abnormal development of the first branchial arch. On day 22 in the human embryo, the branchial arches are forming. The first arch is divided into maxillary and mandibular processes with a horizontal cleft dividing each side at the midline. The mandibular process merges on day 26. A delay in this could result in ectodermal cells with underlying mesodermal cells being deposited in the ventral aspect of the neck. These would continue to differentiate and form skeletal muscle (tongue derivative), salivary glandular tissue, and a mucosal surface, thus resulting in the MCC defect [3, 8]. This second theory explains the absence of hair follicles or sweat or sebaceous glands. It is concluded that the skin protuberance could be a vertical outgrowth of tongue muscle, since the fibrous cord is related to the fibrous median septum of the tongue base; salivary glands in the sinus tract and mucoid discharge contribute to the theory. Usually, MCC is associated with a spectrum of midline anomalies related to the branchial arches, including a median cleft of the lower lip and mandible, hypoplasia, or absence of other midline neck structures [2, 4].
MCC is diagnosed by clinical examination, and the main characteristic is a protruding lesion at the midline of the anterior region of the neck, between the chin and the suprasternal notch. This lesion extends caudally as a longitudinal cleft lined by a reddened epithelium that is most commonly desquamative. Usually, a mucus-secreting opening of the fistulous tract can be found in the most caudal portion of the cleft. Palpation reveals a subcutaneous fibrous cord that extends to the entire cleft or part of it, from the submentonian region to the suprasternal notch . The sinus should be probed and the blind end visualized by radiography. In addition, associated abnormalities of the thyroid gland and other related anomalies should be excluded by ultrasonographic examination. The regional site of the sinus tract is important in distinguishing the MCC from a thyroglossal fistula, since the tract extends caudally in the former and cranially in the latter .
On histological examination, the lesion consists of keratinized stratified squamous epithelium and fibrous tissue and is characterized by the absence of epithelial adnexa in the dermis. Salivary gland tissue and pseudostratified ciliated columnar epithelium are observed in the fistulous tract and in the cyst. In the area of the nipple-like protuberance, there is normal skin, but cartilage and muscle can also be found [3, 10].
Treatment of MCC involves surgical resection and proper reconstruction. Delay in treatment of MCC changes the growth of the lower third of the face and particularly affects mandibular development and extension of the neck . Reconstruction of the defect needs surgical maneuvers other than primary closure, as the primary closure would lead to an unsightly scar and a vertical scar band that would cause restriction of neck movements. Z-plasty is one of the surgical procedures used to close the defect . Single, double, or multiple Z-plasty is the treatment of choice for MCC .
Given the rarity of MCC, we decided to report this case. Our findings are consistent with the literature. Our patient has recovered uneventfully from the surgical treatment.
MCC is an unusual congenital defect that may be encountered by the otolaryngologist, pediatrician, pediatric surgeon, or other health care professional. Surgical excision and reconstruction of the entire defect with multiple Z-plasty reconstruction yields good cosmetic results while improving neck mobility and reducing the risk for long-term cervical tethering and mandibular defects.
No funding sources were used.
Availability of data and materials
All data and material are available for sharing if needed.
MÇ was the primary doctor who treated the patient. He also drafted the manuscript. EA participated throughout these processes. GD helped with the pathological examinations and drafting the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
This report was prepared in accordance with the ethical standards of the institutional ethics committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Informed consent was obtained from the individual participant included in this study.
Consent for publication
Written informed consent was obtained from the patient’s legal guardian(s) for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
The authors declare that they have no competing interests.
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