ICD-10 Specific code C31: Malignant neoplasm of accessory sinuses

Specific codes in ICD-10 are unique alphanumeric designations used to identify and categorize diseases, disorders, and conditions. They consist of 3-5 characters, including both letters and numbers, that provide a high level of detail and specificity.

Translations

Language Translation
Flag for English language  English Malignant neoplasm of accessory sinuses
Flag for French language  French Tumeur maligne des sinus de la face

Hierarchical position

Level Code Title
1 II Neoplasms
2 C00-C97 Malignant neoplasms
3 C30-C39 Malignant neoplasms of respiratory and intrathoracic organs
4 C31 Malignant neoplasm of accessory sinuses

Contents

Code Title
C31.0 Malignant neoplasm: Maxillary sinus
C31.1 Malignant neoplasm: Ethmoidal sinus
C31.2 Malignant neoplasm: Frontal sinus
C31.3 Malignant neoplasm: Sphenoidal sinus
C31.8 Malignant neoplasm: Overlapping lesion of accessory sinuses
C31.9 Malignant neoplasm: Accessory sinus, unspecified

Indicated medicines

Active Ingredient Description
Ifosfamide

Ifosfamide is an antineoplastic, a cytotoxic alkylating agent. It is a prodrug and shows no in vitro cytotoxic activity until activated by microsomal enzymes. The cytotoxic activity of ifosfamide (alkylation of the nucleophilic centres in the cells) is associated with the activated oxazaphosphorine ring hydroxylated at the C4 atom which interacts with DNA-DNA cross linking. This activity manifests itself by blocking the late S and early G2 phases of the cell cycle.

Ipilimumab

Ipilimumab is a CTLA-4 immune checkpoint inhibitor that blocks T-cell inhibitory signals induced by the CTLA-4 pathway, increasing the number of reactive T-effector cells which mobilize to mount a direct T-cell immune attack against tumour cells.

Pembrolizumab

Pembrolizumab is a humanised monoclonal antibody which binds to the programmed cell death-1 (PD-1) receptor and blocks its interaction with ligands PD-L1 and PD-L2. The PD-1 receptor is a negative regulator of T-cell activity that has been shown to be involved in the control of T-cell immune responses.