Parotid cleft cyst is a congenital condition that is usually slow-growing and usually occurs in people in their 30s. There are no clear criteria for the size of the masses, which can vary in size and can be single or multiple. The size of the masses is not clearly defined and can be single or multiple. They occur in the head, face, and neck and are often combined with fistulas, resulting in secondary infections and fever, pain, and other discomforts. The bursa of a cheek cleft cyst may appear as a clear, bright yellow plasma, or in some cases as a white emulsion or a yellowish-brown viscous fluid. Depending on the site of onset, they can be classified as first and second cheek cleft cysts, and third and fourth cheek cleft cysts. The most common cyst is the second cheek cleft cyst in the upper neck, while the first cheek cleft cyst is less common and the third cheek cleft cyst is the least common. If the patient has similar symptoms, it is recommended to go to the hospital for examination as soon as possible. In addition, the disease is prone to recurrent infections, so timely treatment at regular hospitals is needed.