Accessory Parotid Gland Research Articles

Surgical treatment of accessory parotid gland tumours

An accessory parotid gland is located preauricular buccal area and it's duct is separated from main duct of parotid gland. Tumours arised from accessory parotid gland is not so often, however, we experienced five cases with tumours considered to develope from the accessory parotid gland from 1996 to 2010. All tumours were performed the surgical removal under the general anaesthesia. The skin-incision lines were used the sigmoid-like temporal-preauricular-submandibular incision lines according to the peripheral technique for the conservation of facial nerves.

Review of accessory parotid gland tumors: Pathologic incidence and surgical management

ObjectiveThe current study presents our experience with accessory parotid gland masses and reviews the literature on accessory parotid tumor incidence and surgical management. Based on our results, we advocate a standard parotidectomy approach with routine facial nerve dissection at the time of excision. Study DesignWe performed a retrospective chart review and comprehensive literature review on incidence of accessory parotid gland neoplasms. MethodsA retrospective chart review of all patients with mid-cheek masses treated by the senior author was conducted from January 2003 to January 2009. The tumor size at presentation, FNA biopsy, pathologic diagnosis, and surgical treatment were recorded for 13 patients. ResultsIn the case series, 54% of lesions were benign (n=7) and 46% were malignant (n=6) including benign pathologies of 4 pleomorphic adenomas, 2 lymphadenitis, 1 monomorphic adenoma and malignant pathologies of 2 mucoepidermoid carcinoma, 2 B-cell lymphomas, 1 adenocarcinoma, and 1 myofibrosarcoma. Surgical intervention was performed on all patients with standard parotidectomy incision for accessory parotid mass excision after identification and tracing of facial nerve and its branches. ConclusionThe present study provides support for a standard parotid incision with identification of the facial nerve at the time of surgical incision as this resulted in successful excision of accessory parotid tumors with favorable cosmetic results and without facial paralysis or tumor recurrence. Literature review of 152 cases of accessory parotid gland lesions, revealed a pooled incidence of 70% benign and 30% malignant.

Solitary fibrous tumor of the accessory parotid gland: a unique case

Solitary fibrous tumors are benign spindle-cell neoplasms, mostly originating from the visceral pleura. They are common in individuals aged 20-70 with no sex predilection. To our knowledge, this is the unique case of the solitary fibrous tumor originating from the accessory parotid gland in the literature.

Salivary Duct Carcinoma of the Accessory Parotid Gland

Objective: 1) Present a rare case of salivary duct carcinoma of the accessory parotid gland (APG). 2) Understand the current prevalence, diagnosis, and management of benign and malignant tumors of the APG.Method: This study includes a case presentation and literature review. The literature review included articles from October 1966 to January 2010 and included all cases of accessory parotid gland tumors in adults.Results: One hundred and nineteen cases with 19 different tumor types were reported in the accessory parotid gland (APG). Pleomorphic adenoma and mucoepidermoid carcinoma represented 50% and 23%, respectively. There were no previously reported salivary duct carcinomas of the APG. Forty percent of APG neoplasms were malignant. This malignancy rate was comparable to previous studies reporting a higher rate of malignant tumors in the APG compared with 15% to 20% in parotid tumors. A standard parotidectomy remains the preferred approach with less risk to the facial nerve compared with direct cheek re...

A case of myoepithelioma emerging in the buccal region: verification of the primary site based on magnetic resonance imaging, computed tomography, histopathological, and anatomical findings

A case of myoepithelioma presumed to have arisen from an accessory parotid gland is reported. Preoperative fine-needle aspiration cytological findings suggested a malignant tumor, possibly an adenoid cystic carcinoma, while histopathological findings acquired during surgical resection revealed a myoepithelioma. The tumor was located adjacent to the Stensen duct, suggesting an accessory parotid gland origin. The diagnostic potential of magnetic resonance imaging and contrast-enhanced computed tomography in diagnosing this disease is discussed.

Pleomorphic adenoma of the accessory parotid gland misdiagnosed as glomus tumour

Accessory parotid gland tumours are rare and should be included in the differential diagnosis of neoplasms in the midcheek region.

Minor Salivary Gland Neoplasm in Children

In this article, we present a review of the literature, and we focus on 2 particular cases of cancer of the salivary glands accessory in pediatric patients The accessory parotid is the site of congenital and acquired lesions. In adults, the acquired lesions are often neoplastic and are usually similar to those seen in the main parotid gland. The disorders in children are less well defined, as only a few cases have been reported.The accessory parotid gland, or accessory parotid, is a nodule of normal salivary tissue separated from the main parotid gland, located on the masseter muscle, to which it is bound by an extension of the masseteric fascia and connected to the Stensen duct at that level. In contrast to the extensive literature on acquired lesions of the accessory parotid in adults, very few cases of malignant or benign lesions of the accessory parotid in children could be found in the literature. A review of several articles reporting lesions of the accessory parotid in adult patients, reporting 3 or more cases each for a total of 71 patients, showed 24 malignant neoplasms, 39 benign neoplasms, and 8 nonneoplastic lesions. Lesions of the accessory parotid are quite rare in children but should be considered when facing mass located in the cheek.

Coincidental Tumors in the Main and an Accessory Parotid Gland

Introduction. We are presenting a rare case of a patient who developed simultaneous tumors in the main parotid gland (MPG) and an accessory parotid gland (APG). The APG tumor was not recognized when the more prominent MPG tumor was excised. We will discuss the clinical features of this case. Case presentation. A 66-year-old woman was referred to our department with a painless right cheek mass. Her past medical history was notable for a right MPG tumor excision at the age of 62. A retrospective review of the original MRI films revealed that a small APG tumor was present prior to the removal of the MPG tumor. Conclusion. Although the coincidental presence of the MPG and APG tumors is quite rare, this case shows the importance of iden- tifying the smaller and potentially more sinister lesion involving the APG when it is present while preparing for the MPG tumor excision.

S-shaped Incision Approach for a Pleomorphic Adenoma Arising from the Accessory Parotid Gland

S-shaped Incision Approach for a Pleomorphic Adenoma Arising from the Accessory Parotid Gland

Unilateral Parotid Agenesis Associated with Pleomorphic Adenoma of Ipsilateral Accessory Parotid Gland

Congenital agenesis of the parotid gland is rare, and its association with accessory parotid tissue is even rarer. We report an unusual case of unilateral agenesis of the left parotid gland associated with pleomorphic adenoma of the left accessory parotid gland. To best of our knowledge, this is only the second such published case in the literature.

副耳下腺腫瘍の臨床的検討

Accessory parotid gland tumors are relatively rare; hence, adequately detailed clinical analyses of these tumors are difficult to perform at a single institution. In this report, we describe the findings for 65 patients [29 men, 36 women; median age, 51 (9-81) years] with accessory parotid gland tumors, consisting of 4 cases documented by us and 61 cases previously reported by other Japanese authors. Approximately 50% of the patients were treated in an otolaryngology department, while the remaining patients were treated in plastic surgery, oral surgery, or dermatology departments. In 4 patients, the results of preoperative fine-needle aspiration cytology indicated that the tumor was benign; however, the postoperative histopathology results revealed malignant tumors. The frequencies of malignant and benign tumors were 44.6% (n = 29) and 55.4% (n = 36), respectively. Mucoepidermoid carcinoma and pleomorphic adenoma were the most frequent types of malignant and benign accessory parotid gland tumors, respectively. Among the various surgical methods that were used, such as direct cheek and intraoral incisions, a standard parotidectomy incision was the most preferred treatment approach for these tumors. Recently, an endoscopic approach has also been found to yield satisfactory results. An optimal approach should be selected after evaluating the advantages and disadvantages of these methods. No definite guidelines are available regarding the choice of elective neck dissection and postoperative radiation therapy for malignant accessory parotid gland tumors. Although tumor resection (plus elective neck dissection) and postoperative radiation therapy have been frequently performed for various kinds of malignant accessory parotid gland tumors to date, additional studies are needed regarding the criteria for selecting elective neck dissection and postoperative radiation therapy. Since the malignancy rate for accessory parotid gland tumors is higher than that for parotid gland tumors, the possibility of malignancy (especially mucoepidermoid carcinoma and carcinoma ex pleomorphic adenoma) should be considered when resecting accessory parotid gland tumors, even if the results of preoperative fine-needle aspiration cytology indicate that the tumor is benign.

Accessory parotid gland tumor: A report of six cases

Accessory parotid gland tumor: A report of six cases

The salivary ducts of Wharton and Stenson: Analysis of normal variant sialographic morphometry and a historical review

Submandibular and parotid salivary glands acquire lengthy ducts as they migrate during development. No conclusive reports exist on clinically important anatomical normal variants and morphometry of the submandibular duct of Wharton and the parotid duct of Stenson. We retrospectively analyzed 67 normal digital subtraction sialograms on patients ranging from 16 to 85 years of age (M:F=15:52). In 43 sialograms, the mean parotid duct length was 50 mm. The mean width of the proximal, mid, and distal segments of the parotid duct were 1.8 mm, 1.1 mm, and 1.6 mm, respectively. An accessory parotid gland was present in 68% of patients, with a mean angle of confluence of its tributary duct with the parotid duct of 53°. In 24 sialograms the mean length of the submandibular duct was 58 mm. The mean width of the proximal, mid, and distal segments of the submandibular duct were 2.0 mm, 2.7 mm, and 2.1 mm, respectively. The submandibular duct genu had a mean angle of 115°. The effect of independent variables (age, gender, and side) was statistically tested on the dependent variables (length, mean calibre, and angle) using regression analysis. None of the independent variables affected variations in length, size and angulation. These reported comprehensive and detailed morphometrics are useful for therapeutic planning of luminal procedures on the salivary ducts, including sialography, sialoendoscopy, interventional therapies, and lithotripsy.

Congenital sialoblastoma of the accessory parotid gland

Sialoblastomas are rare, locally aggressive, perinatal or congenital salivary gland tumours that mostly originate in the parotid gland. Significant variability in histological range and clinical course exists. This report is of a case of congenital sialoblastoma of the accessory parotid gland.

Congenital sialoblastoma of the accessory parotid gland

Sialoblastomas are rare, locally aggressive, perinatal or congenital salivary gland tumours that mostly originate in the parotid gland. Significant variability in histological range and clinical course exists. This report is of a case of congenital sialoblastoma of the accessory parotid gland.

Minimally invasive endoscopic resection of benign tumours of the accessory parotid gland: an updated approach

The most common conventional approaches for the resection of benign tumours in the accessory parotid gland are a standard parotidectomy incision, a modified standard parotidectomy incision, or a face-lift incision. The resulting scars may severely affect the patient's postoperative appearance. The previously reported endoscopically assisted approach offers a less aesthetically invasive technique, but it may still leave a visible preauricular scar 4–5cm long. We have used a modified endoscopic approach with minimal, and concealed, incisions for the resection of benign tumours in the accessory parotid gland. Five patients were diagnosed by physical examination, imaging, and preoperative fine-needle aspiration biopsy. They had endoscopically assisted resections using our modified approach, and we evaluated its feasibility. All the resections were successful. The mean operating time was 108min (range 90–130). The postoperative scars were concealed and aesthetically satisfactory. There were no facial paralyses, salivary fistulas, or recurrences in the short term. Using endoscopically assisted resection we completely removed benign tumours from the accessory parotid gland and obtained good aesthetic results. Our updated endoscopic approach for these resections is successful with shorter, concealed incisions. It is a viable alternative to conventional approaches.

Salivary Duct Carcinoma of the Accessory Parotid Gland

Objective: 1) Present a rare case of salivary duct carcinoma of the accessory parotid gland (APG). 2) Understand the current prevalence, diagnosis, and management of benign and malignant tumors of the APG. Method: This study includes a case presentation and literature review. The literature review included articles from October 1966 to January 2010 and included all cases of accessory parotid gland tumors in adults. Results: One hundred and nineteen cases with 19 different tumor types were reported in the accessory parotid gland (APG). Pleomorphic adenoma and mucoepidermoid carcinoma represented 50% and 23%, respectively. There were no previously reported salivary duct carcinomas of the APG. Forty percent of APG neoplasms were malignant. This malignancy rate was comparable to previous studies reporting a higher rate of malignant tumors in the APG compared with 15% to 20% in parotid tumors. A standard parotidectomy remains the preferred approach with less risk to the facial nerve compared with direct cheek resection and transoral approaches. Conclusion: Most tumor types that have been identified in the parotid gland have also been found in the APG, including this latest finding of salivary duct carcinoma in the accessory gland. The rate of malignant tumors of the APG appears to be higher than that of the main parotid gland.

Aspiration biopsy of mammary analogue secretory carcinoma of accessory parotid gland: Another diagnostic dilemma in matrix‐containing tumors of the salivary glands

Mammary analogue secretory carcinoma (MASC) is a newly described rare salivary gland tumor, which shares morphologic features with acinic cell carcinoma, low-grade cystadenocarcinoma, and secretory carcinoma of the breast. This is the first reported case of MASC of an accessory parotid gland detected by aspiration biopsy with radiologic and histologic correlation in a 34-year-old patient. Sonographically-guided aspiration biopsy showed cytologic features mimicking those of low-grade mucoepidermoid carcinoma, including sheets of bland epithelial cells, dissociated histiocytoid cells with intracytoplasmic mucinous material, and spindle cells lying in a web-like matrix. Histologic sections showed a circumscribed tumor with microcystic spaces lined by bland uniform epithelial cells and containing secretory material. The tumor cells expressed mammaglobin and BRST-2. The cytologic features, differential diagnosis, and pitfalls are discussed. The pathologic stage was pT1N0. The patient showed no evidence of disease at 1 year follow-up.

A Rare Case of Chronic Sialadenitis of Accessory Parotid Gland

The accessory parotid gland is salivary tissue adjacent to stenson's duct that is separated from the main parotid gland and lying on masseter muscle. It has secondary duct empting into the stenson's duct. The differential diagnosis of mid-cheek masses include pathology arising from normal anatomic structures or from variations of normal accessory parotid gland tissue. Surgical resection is the treatment of choice for the accessory parotid gland tumor. We report a case of accessory parotid gland with chronic sialadenitis in a 26years old male with the diagnosis and treatment. Accessory parotid gland pathologies should be included in the differential diagnosis of a patient presently with a mid-cheek mass.

Wide Excision of Accessory Parotid Gland With Anterior Approach

Accessory parotid gland tissue has been described as salivary tissue adjacent to the Stensen duct that is distinctly separate from the main body of the parotid gland. Of all parotid gland tumors, 1% to 8% arise from the accessory parotid gland. Little is known about the accessory parotid gland, and it is seldom mentioned in the literature. Between 1999 and 2010, we have treated and followed 8 patients with tumors of the accessory parotid gland. There were 5 males and 3 females with a mean age of 35 years. They all presented with an asymptomatic cheek mass, and 4 of them underwent fine-needle aspiration. Ultrasound or computed tomographic scan was used in all patients. All the patients underwent surgical intervention with standard parotidectomy incision and anterior extension. The mean follow-up time was 44 months (range, 6-120 months). Seven patients had benign disease. Four cases were pleomorphic adenoma, and the remaining 3 benign cases were parotid cyst, basal cell adenoma, and hemangioma. Only 1 patient had a malignant tumor that was a lymphoepithelioma-like carcinoma. In 7 cases, wide excision (excision of mass and accessory lobe of the parotid gland) was done because of the intra-accessory parotid gland lesion. One patient had concomitant superficial parotidectomy because the tumor was located very close to and has involved the parotid gland proper. There was no serious postoperative complication and recurrence. Prudent preoperative diagnostic evaluation and meticulous surgical approach are the keys to successful management of midcheek lesions. A wide excision of the accessory lobe of the parotid gland can be a definitive surgery in case of solitary tumor with an intact parotid fascia, and wide excision with anterior approach through a standard parotidectomy incision is preferred to a direct incision over the mass.