Cavernous hemangioma of the parotid gland
Ravi Hari Phulware; Amrita Talwar; Arvind Ahuja
Abstract
Cavernous hemangioma (CH), or cavernoma, is a type of benign tumor occurring mostly in the brain, liver, skin, and retina.
CH is more commonly found in women than men and typically occur between the ages of 40 and 60. Their precise incidence needs to be well-established; however, they account for 2-4% of all parotid gland tumors.
CH is typically diagnosed by imaging tests such as MRI or CT scans. The location, size, symptoms, and general health of the patient are among the variables that affect how cavernous hemangiomas are treated. Treatment options in symptomatic cases with functional impairment and high risk of bleeding, include medical (steroid or interferon), embolization, surgery, or radiosurgery.
Parotid gland tumors can be either benign or malignant. CH of the parotid gland is a relatively rare but well-documented entity in the medical literature. There is currently not enough knowledge on the prevalence of CH in the parotid gland; there were roughly 50 cases reported worldwide, most of which were individual case reports. Overall, the literature suggests that cavernous hemangioma of the parotid gland is a rare benign entity more common in females and typically presents as a painless mass in the parotid gland area. Surgical removal is the primary treatment, and this entity has a good prognosis and a low recurrence risk.
A hemangioma's histopathological appearance can help determine the appropriate management and treatment options. Capillary hemangiomas may be treated with topical or oral medications, while surgical removal may be necessary for cavernous hemangiomas, depending on their size and location.
Treatment options for parotid gland cavernous hemangiomas depend on the lesion’s size and location, the patient's symptoms and overall health status. In some cases, surgical removal of the tumor may be necessary, which can be challenging due to the proximity of the facial nerve and the risk of its injury. In other cases, observation or radiation therapy may be recommended.
Cavernous hemangioma is a type of vascular malformation, but other types of vascular malformations can present with similar symptoms or imaging findings. The differential diagnosis of vascular malformation with cavernous hemangioma includes (i) Venous malformation: a type of vascular malformation that affects veins, and it can look similar to cavernous hemangioma on imaging studies. However, venous malformations typically have a more uniform appearance, while cavernous hemangiomas have a characteristic “popcorn” appearance due to multiple blood-filled spaces; (ii) Capillary malformation: a type of vascular malformation that affects small blood vessels called capillaries. Capillary malformations can present as flat, red, or pink marks on the skin and can sometimes be mistaken for cavernous hemangioma; (iii) arteriovenous malformation: a type of vascular malformation that involves abnormal connections between arteries and veins. Arteriovenous malformations can cause symptoms such as headaches, seizures, and neurological deficits and can be mistaken for cavernous hemangioma on imaging studies; (iv) Lymphatic malformation: a type of vascular malformation that affects the lymphatic vessels and can cause swelling or abnormal growths. Lymphatic malformations can sometimes be mistaken for cavernous hemangioma in imaging studies.
Keywords
References
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Submitted date:
04/21/2023
Accepted date:
05/12/2023
Publication date:
06/12/2023