Malignant neoplasm of sublingual gland
ICD-10 C08.1 is a billable code used to indicate a diagnosis of malignant neoplasm of sublingual gland.
Malignant neoplasms of the sublingual gland are rare tumors that arise from the salivary gland tissue located beneath the tongue. These tumors can be aggressive and may present with symptoms such as swelling, pain, or difficulty swallowing. Imaging studies, including MRI and CT scans, are crucial for diagnosis, as they help delineate the tumor's size, extent, and involvement of surrounding structures. Histopathological examination following biopsy is essential for definitive diagnosis, as these tumors can exhibit various histological types, including adenoid cystic carcinoma and mucoepidermoid carcinoma. Treatment typically involves surgical excision, which may be challenging due to the gland's location and proximity to vital structures. In some cases, adjuvant therapies such as radiation may be indicated, especially if there is a high risk of recurrence. Early detection and appropriate management are critical for improving patient outcomes.
Detailed pathology reports, imaging studies, and treatment plans.
Diagnosis and management of malignant salivary gland tumors, including staging and treatment planning.
Ensure accurate coding of tumor type and treatment modalities.
Operative reports, pre-operative assessments, and post-operative follow-ups.
Surgical excision of sublingual gland tumors and management of complications.
Document the extent of surgical resection and any reconstructive procedures performed.
Used when a malignant neoplasm of the sublingual gland is surgically excised.
Operative report detailing the procedure and findings.
Otolaryngology specialists should ensure accurate coding of the surgical approach and any complications.
Common symptoms include swelling under the tongue, pain, difficulty swallowing, and changes in taste. Patients may also experience numbness or tingling if the tumor affects nearby nerves.
Diagnosis typically involves imaging studies such as MRI or CT scans, followed by a biopsy to confirm malignancy through histopathological examination.
Treatment usually involves surgical excision of the tumor, and in some cases, radiation therapy may be recommended, especially if there is a risk of recurrence.
