STERNOCLEIDOMASTOID (SCM) MUSCLE FLAP AFTER PAROTIDECTOMY
Journal Title: Journal of Evolution of Medical and Dental Sciences - Year 2018, Vol 7, Issue 6
Abstract
BACKGROUND Parotidectomy1 is a routinely undertaken procedure by general surgeons and ENT surgeons; however, the risk of facial nerve injury and further deformity is a scare of the patient and nightmare of the operating surgeon, thus obtaining consent for the surgery is a difficult task of the surgeon. Most patients are happy after surgery; however, a depressed facial contour is a point of significant dissatisfaction for the patient. Another point of concern after superficial or total parotidectomy is Frey syndrome, 2 which is seen in almost 80%, 2 but becomes noticed or symptomatic only in about 10% - 12%.2 Many a number of attempts have been made with fascia lata, dermal fat, platysma, temporalis fascia, sternocleidomastoid muscle and submuscular aponeurotic sheath of the face to overcome these disabling issues. The sternocleidomastoid muscle flap with its superiorly based perfusion from occipital artery and superior thyroid artery is an effective tool in preventing Frey syndrome and avoiding a pitted deformity in the periauricular region, thus achieving facial symmetry. The advantage of this muscle over the other alternatives described is that it has lower chance of necrosis and it provides cover over a larger area and its design is easier. The objective of the study was to assess the cosmetic and functional outcome of primary sternocleidomastoid muscle flap undertaken on post parotidectomy patients with reference to the cosmetic outcome, occurrence of Frey syndrome and sensation to the ear lobe. MATERIALS AND METHODS This descriptive study was undertaken on 22 patients, among whom 14 underwent superficial parotidectomy and 8 total conservative parotidectomy. RESULTS Among the 22 patients who underwent the procedure after parotidectomy, 4 were males and 18 were females. There were 14 superficial parotidectomy and 8 total conservative parotidectomy. The histopathology report was malignancy in 6 patients, pleomorphic adenoma in 14 patients and Warthin’s tumour in 2. Satisfactory cosmetic outcome was possible in 21 patients. One patient had marginal necrosis of the flap and a pitted scar (post radiation patient) requiring PMMC (pectoralis major myocutaneous flap) cover. Frey syndrome occurred in one patient in spite of the flap. Ear lobule sensation was preserved in 20/22 patients. CONCLUSION Partial thickness superiorly based on sternocleidomastoid flap3,4 provides exemplary cosmetic outcome following either superficial or total conservative parotidectomy and it significantly lowers the incidence of Frey syndrome.
Authors and Affiliations
Ramraj R, Vishnu M. L
PLEOMORPHIC XANTHOASTROCYTOMA WITH ANAPLASTIC FEATURES- A RARE CASE REPORT AND REVIEW OF LITERATURE
PRESENTATION OF CASE A 42-year-old healthy woman complained of headache, imbalance while walking with slurring of speech with weakness in right upper and lower limbs with deviation of mouth evolving over 15 days. CT brai...
SEX DIFFERENCES IN THE CONGENITAL ANOMALIES: A HOSPITAL BASED CROSS SECTIONAL STUDY
BACKGROUND The present study was conducted with an aim to study the sex differences in various congenital anomalies, overall and by subtype. MATERIAL AND METHOD This cross sectional study was carried out in...
PRIMARY TRANSITIONAL CELL CARCINOMA OF THE OVARY: A CASE REPORT
A 38-year-old female presented with a history of progressively enlarging abdominal mass. Abdominal computed tomography showed a pelvic mass involving both the ovaries and omentum. CA-125 was normal. Staging surge...
IMPACT OF NUCHAL CORD ON INTRAPARTUM COMPLICATIONS, MODE OF DELIVERY AND PERINATAL OUTCOME
BACKGROUND Umbilical cord forms the connecting link between foetus and placenta through which blood flows to and from the placenta and is the lifeline of foetus. Cord accidents lead to 5-18% of all fatal foetal asphyxia...
TAR (THROMBOCYTOPENIA WITH ABSENT RADIUS) SYNDROME WITH CONGENITAL ACYANOTIC HEART DISEASE: A RARE CASE REPORT
It is a rare genetic disorder characterized by the absence of the radius bone in the forearm and a dramatically reduced platelet count. This syndrome may occur as a part of the 1q21.1 deletion syndrome. Symptoms...