Adenoid cystic carcinoma

Adenoid cystic carcinoma
Synonyms	ACC
Pronounce	N/A
Specialty	N/A
Symptoms	Pain, swelling, numbness, facial nerve paralysis
Complications	Metastasis, recurrence
Onset	Middle age
Duration	Long-term
Types	Cribriform, tubular, solid
Causes	Unknown
Risks	Radiation exposure, genetic predisposition
Diagnosis	Biopsy, imaging studies
Differential diagnosis	Pleomorphic adenoma, mucoepidermoid carcinoma
Prevention	None
Treatment	Surgery, radiation therapy, chemotherapy
Medication	Cisplatin, doxorubicin
Prognosis	Variable, often poor in advanced stages
Frequency	Rare
Deaths	Varies

== Adenoid Cystic Carcinoma ==

Histological image of adenoid cystic carcinoma

Adenoid cystic carcinoma (ACC) is a rare type of cancer that most commonly arises in the salivary glands. It is known for its slow growth, tendency to invade surrounding nerves, and potential for distant metastasis.

Pathophysiology

Adenoid cystic carcinoma is characterized by its unique histological appearance, which includes cribriform, tubular, and solid patterns. The tumor is composed of small, basaloid cells that form pseudocystic spaces filled with hyaline material. ACC is notorious for its perineural invasion, which can lead to significant neurological symptoms.

Clinical Presentation

Patients with adenoid cystic carcinoma often present with a painless mass in the affected gland, most commonly the parotid gland or submandibular gland. Due to its propensity for perineural invasion, patients may also experience facial nerve paralysis or other cranial nerve deficits.

Diagnosis

Diagnosis of ACC is typically made through a combination of imaging studies and biopsy. MRI is particularly useful for assessing perineural spread, as seen in the images below:

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  Coronal MRI showing right parotid adenoid cystic carcinoma with perineural spread.

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  MRI showing perineural spread of adenoid cystic carcinoma along the facial nerve.

Histopathology

Histological examination reveals the characteristic cribriform pattern of ACC. Immunohistochemical staining, such as S-100, can aid in diagnosis:

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  Histological section of adenoid cystic carcinoma.

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  S-100 staining of adenoid cystic carcinoma.

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  Cytological image of adenoid cystic carcinoma.

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  Adenoid cystic carcinoma with comedonecrosis.

Treatment

The primary treatment for adenoid cystic carcinoma is surgical resection with clear margins. Due to the high risk of perineural invasion, adjuvant radiation therapy is often recommended. Chemotherapy is generally reserved for metastatic disease.

Prognosis

The prognosis for patients with adenoid cystic carcinoma varies depending on the stage and location of the tumor. While the tumor is slow-growing, it has a high rate of local recurrence and distant metastasis, particularly to the lungs.

Epidemiology

Adenoid cystic carcinoma accounts for approximately 1% of all head and neck malignancies. It is more common in women and typically presents in middle-aged adults.

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  Relative incidence of submandibular tumors.

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  Relative incidence of parotid tumors.

Related Pages

• Salivary gland tumors
• Perineural invasion
• Parotid gland
• Submandibular gland

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  Adenoid cystic carcinoma - intermediate magnification

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  Coronal MRI showing right parotid adenoid cystic carcinoma with perineural spread of tumor

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  MRI showing perineural spread of adenoid cystic carcinoma along the facial nerve

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  Adenoid cystic carcinoma

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  Adenoid cystic carcinoma (S-100)

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  Adenoid cystic carcinoma cytology

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  Adenoid cystic carcinoma with comedonecrosis

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  Relative incidence of submandibular tumors

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  Relative incidence of parotid tumors