A Giant Pleomorphic Adenoma of the Submandibular Salivary Gland: A Case Report

Abstract

The most common benign salivary gland tumor is the pleomorphic adenoma (PA). They can attain grotesque proportions and weigh several kilograms. They can cause facial disfigurement and, if untreated, could lead to airway compromise. We report a case of a large PA arising from the left submandibular salivary gland in a 20-year-old black female. The lesion measured ~16 × 15 × 12 cm.

Pleomorphic adenoma (PA) is the most common salivary gland tumor in both the major and minor salivary glands. They are also referred to as “benign mixed tumors.” They represent 60 to 80% of all benign tumors in major salivary glands and 40 to 70% of minor salivary glands [1].

These tumors are slow-growing and painless. However, failure to seek early treatment can result in grotesque facial deformity [2]. They are also reported to occur in the main bronchus, columella, larynx, pharynx, trachea, lacrimal gland, sinonasal tract, and maxillary sinus, albeit less commonly [3]. Neck lymphadenopathy and nerve compromise are generally absent [2]. The purpose of this article is to emphasize that although the PA is a well-reported entity, they can attain very large sizes and, if left untreated, could also lead to the airways being compromised. We report a case, which to the best of the author’s knowledge is the largest PA of the submandibular gland.

Case Report

A 20-year-old black woman of cross-border nationality, presented to our maxillofacial and oral surgery department seeking medical attention for a large swelling on the left side of her jaw (Figure 1A,B). The swelling was painless with a history of having increased in size over an 8-year period. She noticed the swelling for the first time at the age of 12. The patient was otherwise healthy with no other significant medical history or findings.

On examination, the weight of the swelling tilted the patient’s head to the left. The swelling was multinodular, nontender, hard, and mobile. Movement of the tumor mass could be elicited and palpated bimanually both intraorally (in the region of the left submandibular salivary gland) and extraorally over the mass simultaneously.

The advancing “apex” of the tumor had ulcerations and scars suggestive of previous biopsies having been done in her country of origin (Figure 2C). The patient confirmed having had an unreported previous biopsy. Submandibular lymph nodes could not be palpated due to the tumor mass. No other supraclavicular nodes were palpable. The lesion was diagnosed clinically as a PA.

Micrograph of the incisional biopsy that was done showed features of a myxochondroid and cellular PA. The cartilage and myxoid areas grew in nodules with cellular areas in between. No mitotic activity was present and the tumor capsule could not be identified (Figure 2B). The diagnosis of PA was confirmed.

Imaging studies included an orthopantomograph, PA mandible, and computed tomography (CT; Figure 1A,D and Figure 2A). CT showed a large homogenous mass involving the left submandibular space and left anterior cervical space with superior abutment of the left parotid gland. Diffuse calcifications were found within the lesion. The epicenter of the tumor was within the submandibular gland. There was medial extension to the left parapharyngeal space. Bony elements of the maxilla and mandible were within normal limits.

An en bloc resection of the tumor was done with preservation of the overlying nonulcerated skin (Figure 2D and Figure 3A–D).

The patient recovered well and was discharged on day 4 postoperatively. Patient review was uneventful and the incision wound healed well (Figure 4D).

Discussion

There is consistency in published reports showing the PA to be the commonest of the salivary gland tumors. Certainly in one of the largest studies involving 6982 primary salivary gland tumors in a Chinese population by Tian et al., PA was the most common tumor (69%) of which only 20% were located in minor salivary glands [4]. They have been reported to be as large as 28 × 20 × 16 cm in the parotid gland [5]. Gupta et al. reported weights of PAs ranging from 1 kg to 27 kg [6]. The occurrence of very large PAs in the submandibular gland are rare and reports of 8 × 6 × 4 cm have been documented [6]. Our case measured 16 × 15 × 12 cm.

They are epithelially derived and typically present as a cytologically benign circumscribed mass with variable encapsulation. Histomorphologically, it is characterized by a variegated architecture comprising epithelial elements admixed with a mucoid, myxoid, fibrohyaline, or chondroid stoma. Historically, the main clinical problems with PA have been the risk of recurrence and progression to a clinically or histologically based malignancy [7].

The rate of tumor recurrence seems to depend on surgical techniques used as this could contribute to intrasurgical rupture and tumor spillage with resultant seeding of tumor cells. Histopathologic features may also impact on the rate of recurrence. In a study of 225 patients with PA, Henriksson et al. found 56% of the PAs that had recurred showed fingerlike tumor extensions or pseudopodia outside the pseudocapsule microscopically as compared with the 25% of recurrences in patients who had intraoperative rupture of the tumor [8].

Over recent years, there has emerged a rare but nonetheless well-documented subgroup of PA entities that require additional awareness and precise recognition in terms of their propensity for future aggressiveness. These include features of vascular invasion, focal dysplasia, and noninvasive (intracapsular) carcinoma ex pleomorphic adenoma [7].

Generally, malignant transformation can be suspected with a sudden increase in size accompanied by local signs of malignancy, pain, ulceration, spontaneous bleeding, and superficial and deep tissue invasion. Furthermore, multiple recurrences and the size of the tumor may play a role in the malignant transformation of the PA. The clinical characteristics of malignant transformation have been reported in the literature as (1) a long history of PA, (2) advanced age, (3) location in a major salivary gland, and (4) history of rapid growth associated with pain or ulceration [7]. Age in our case was to the patient’s advantage. Representative microscopic sampling of large PAs is important to rule out malignant change, which could increase in frequency with large tumors as malignant sites could be missed.

Reporting a case of this nature has significance as delayed intervention allows for rapid tumor growth (believed by some to be due to mutated ras genes [9]), poor aesthetics, psychological trauma, and a possible threat to life especially with the presence of tumor pressure over the parapharyngeal space and oropharynx, which could be compounded by infection thus threatening the airway. The expanding mass could further distort the anatomy thus displacing vital structures and making the dissection more challenging. The possible location of nerves and blood vessels are depicted in (Figure 5). The presentation of cases such as the one being reported highlights the plight of many patients especially in the developing nations. Whatever the reasons; such disease progression should never be condoned, certainly not in the twenty-first century.