What are the other Names for this Condition? (Also known as/Synonyms)

• Salivary Gland Juvenile Cellular Pleomorphic Adenoma

What is Juvenile Cellular Pleomorphic Adenoma of Salivary Gland? (Definition/Background Information)

• A pleomorphic adenoma of salivary gland is the most common benign tumor arising from the salivary tissue. It may be present in individuals of a wide age range, but typically adults are affected
• A Juvenile Cellular Pleomorphic Adenoma of Salivary Gland is an uncommon pleomorphic adenoma that occurs in young individuals (children and adolescents). The tumors mostly arise in the major salivary glands, and sometimes, in the minor salivary glands
• The cause of formation of the tumor is unknown, although a few genetic abnormalities have been identified. A prior history of radiation therapy to the region may be a contributing factor towards development of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland
• Most tumors are solitary, small, and asymptomatic. The larger tumors may compress the surrounding structures and cause related signs and symptoms. Sometimes, multiple tumors may be noted that either involve other salivary glands or the same gland
• The diagnosis of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland can be confirmed through a tissue biopsy. The treatment is a complete surgical removal of the tumor with adequate margins
• The prognosis of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland is generally excellent with adequate treatment (complete removal through surgery). However, tumor recurrences are not uncommon, and some are even known to undergo malignant transformations

Who gets Juvenile Cellular Pleomorphic Adenoma of Salivary Gland? (Age and Sex Distribution)

• Juvenile Cellular Pleomorphic Adenoma of Salivary Gland is generally uncommon
• The tumor is present in children and teens, usually up to age 18-20 years
• The condition is slightly more common in females, though both males and females are affected
• All races and ethnic groups may be affected

What are the Risk Factors for Juvenile Cellular Pleomorphic Adenoma of Salivary Gland? (Predisposing Factors)

• No clearly identified risk factors for Juvenile Cellular Pleomorphic Adenoma of Salivary Gland have been established to date
• A history of radiation therapy to the head and neck region may be a risk factor for the development of pleomorphic adenoma of salivary gland. The radiation treatment may have been undertaken even 15-20 years’ ago

It is important to note that having a risk factor does not mean that one will get the condition. A risk factor increases one’s chances of getting a condition compared to an individual without the risk factors. Some risk factors are more important than others.

Also, not having a risk factor does not mean that an individual will not get the condition. It is always important to discuss the effect of risk factors with your healthcare provider.

What are the Causes of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland? (Etiology)

Currently, the cause of formation of Juvenile Cellular Pleomorphic Adenomas of Salivary Gland is unknown.

• However, based on extensive studies, pleomorphic adenomas have shown chromosomal rearrangements, translocations, and other genetic abnormalities
• Some studies have also informed about the involvement of the cancer-causing virus SV40 (simian virus 40). It is researched that this virus may provoke the development of salivary gland pleomorphic adenoma

What are the Signs and Symptoms of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland?

The signs and symptoms of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland may include:

• Most tumors are confined to the major salivary glands; i.e., to the parotid glands, followed by the submandibular glands
• Some tumors may occur in the minor salivary glands. If tumors occur within the minor salivary gland of the oral mucosa, it is called intraoral pleomorphic adenoma
• When the minor salivary glands are involved, the presence of a tumor mass in the mouth, affecting the soft and hard palate, the inner cheek, or the lips, may be noted
• The mass may be smooth, firm, and mobile; the tumors may appear to be covered by a mucus-coated capsule (from the inside of the mouth)
• Tumors are typically solitary, but multiple lesions that arise from the same gland or from other salivary glands may be noted
• The tumors are well-defined and spherical or oval
• The size may average around 2 cm, although some can grow to very large sizes
• Small tumors usually do not cause any symptoms. Pain is generally not felt, unless the surrounding structures are compressed
• Large tumors may cause skin inflammation and redness

Large tumors may cause the following signs and symptoms:

• Difficulty in opening one’s mouth; pain while eating (pain may be felt in the mouth and face)
• Numbness of part of the face
• Dryness of mouth
• Inability to move one side of the face due to damage to the facial nerve, known as facial nerve palsy
• Facial pain
• Breathing difficulty

How is Juvenile Cellular Pleomorphic Adenoma of Salivary Gland Diagnosed?

The following exams and procedures may be used in the diagnosis of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland:

• Evaluation of the individual’s medical history and a through physical examination
• Plain X-ray of the head and neck region
• Ultrasound scan of the affected salivary gland
• CT or CAT scan with contrast of the head and neck may show a tumor mass. This radiological procedure creates detailed 3-dimensional images of structures inside the scanned region
• MRI scans of head and neck region: A magnetic field is used to create high-quality pictures of certain parts of the body, such as tissues, muscles, nerves, and bones. These high-quality pictures may reveal the presence of the tumor
• Fluorescence in situ hybridization (FISH): It is a test performed on the blood or bone marrow cells to detect chromosome changes (cytogenetic analysis). The test helps in identifying genetic abnormalities that may not be evident with an examination of cells under a microscope
• Polymerase chain reaction (PCR): It is used to measure the presence of certain biomarkers in blood or bone marrow cells. The test is ultrasensitive and detects extremely low amounts of biomarkers remaining in blood, which can be missed by cytogenetic methods, such as FISH, karyotype, or flow cytometry. PCR allows a more sensitive follow-up of patients in remission and can help determine whether additional treatment is necessary

Although the above modalities can be used to make an initial diagnosis, a tissue biopsy of the tumor is necessary to make a definitive diagnosis to begin treatment. The tissue for diagnosis can be procured in multiple different ways which include:

• Fine needle aspiration (FNA) biopsy of the tumor: A FNA biopsy may not be helpful, because one may not be able to visualize the different morphological areas of the tumor. Hence, a FNA biopsy as a diagnostic tool has certain limitations, and an open surgical biopsy may be recommended.  
• Salivary gland core biopsy of the tumor
• Salivary gland open biopsy of the tumor

Tissue biopsy:

• A tissue biopsy of the tumor is performed and sent to a laboratory for a pathological examination. A pathologist examines the biopsy under a microscope. After putting together clinical findings, special studies on tissues (if needed) and with microscope findings, the pathologist arrives at a definitive diagnosis. Examination of the biopsy under a microscope by a pathologist is considered to be gold standard in arriving at a conclusive diagnosis
• Biopsy specimens are studied initially using Hematoxylin and Eosin staining. The pathologist then decides on additional studies depending on the clinical situation
• Sometimes, the pathologist may perform special studies, which may include immunohistochemical stains, molecular testing, and very rarely, electron microscopic studies to assist in the diagnosis

Apart from ruling out other salivary gland tumors, a differential diagnosis to eliminate the following tumors/conditions are often considered, before arriving at a definitive diagnosis:

• Adenoid cystic carcinoma
• Buccal space abscess
• Dermoid cyst
• Fibroma
• Foreign body reaction
• Lipoma
• Mucocele
• Mucoepidermoid carcinoma (MEC)
• Neurofibroma
• Oncocytoma
• Rhabdomyosarcoma

Note:

• The stroma of the tumor, when examined under a microscope by a pathologist, displays cellular features. Hence, it is known as cellular pleomorphic adenoma
• Since Juvenile Cellular Pleomorphic Adenoma of Salivary Gland arises in younger individuals, it can be misdiagnosed, because it is an uncommon tumor

Many clinical conditions may have similar signs and symptoms. Your healthcare provider may perform additional tests to rule out other clinical conditions to arrive at a definitive diagnosis.

What are the possible Complications of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland?

The following complications due to Juvenile Cellular Pleomorphic Adenoma of Salivary Gland may be observed:

• Severe emotional stress and cosmetic concerns (facial disfigurement)
• Large tumors may show the presence of multiple tiny satellite nodules around the main mass
• Even though rare, the tumors are known to recur following surgery to remove them, particularly in younger individuals. Also, long-term recurrences (even after 10 years) have been observed
• Tumors that recur are known to appear widespread in the oral cavity; they are usually multifocal (arising simultaneously at many locations). The treatment in such cases may be difficult or complicated
• Occasionally, pleomorphic adenomas are known to transform into malignant tumors. Although, this may take place over 10-15 years
• Surgery to remove the tumor mass may result in facial nerve palsy (surgical complication)
• Post-surgical wound infection

How is Juvenile Cellular Pleomorphic Adenoma of Salivary Gland Treated?

• A complete surgical excision with clear or wide margins is the preferred mode of treatment of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland. When tumors involve the parotid gland, a superficial parotidectomy is the treatment of choice
• Tumor recurrence may lead to a need for multiple surgeries and more extensive therapies
• Post-operative care is important: One must maintain minimum activity levels, until the surgical wound heals
• Long-term follow-up is required, because recurrence at the site of surgery have been reported many years (even decades) after surgery

How can Juvenile Cellular Pleomorphic Adenoma of Salivary Gland be Prevented?

• Current medical research has not established a method of preventing the formation of Juvenile Cellular Pleomorphic Adenoma of Salivary Glands
• Regular medical screening at periodic intervals with blood tests, radiological scans, and physical examinations, for those who have already endured the tumor, are helpful

What is the Prognosis of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland? (Outcomes/Resolutions)

• The prognosis of Juvenile Cellular Pleomorphic Adenoma of Salivary Gland is generally excellent with surgical intervention and complete removal, since it is a benign tumor
• However, some tumors are known to recur and recurrent tumors may be disseminated across the oral cavity affecting adjoining structures/regions. It is typically difficult and challenging to remove them in such cases
• Besides recurrence, malignant transformations have been infrequently noted. In such cases, the prognosis is based on several factors, including on the stage of the tumor

Additional and Relevant Useful Information for Juvenile Cellular Pleomorphic Adenoma of Salivary Gland:

There are 3 major types of salivary glands and these include the following:

• Parotid glands, found on the sides of the face
• Submandibular glands located at the back of mouth, on both sides of the jaw
• Sublingual glands that are seen under the floor of the mouth

The salivary glands produce saliva that helps in:

• Lubricating the mouth
• Swallowing
• Protects the teeth against bacteria
• Digestion of food