Adenoid cystic carcinoma

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(Redirected from Adenoid cystic cancer)


Adenoid cystic carcinoma
Micrograph of 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 ==
File:Adenoid cystic carcinoma - intermed mag.jpg
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[edit]

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[edit]

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[edit]

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:

Histopathology[edit]

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

Treatment[edit]

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[edit]

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[edit]

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.

Related Pages[edit]

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