C15.8
ICD-10-CMThis code signifies a primary malignant tumor that originates in, or extends across, two or more contiguous sub-sites of the esophagus, making it impossible to assign the neoplasm to a single specific sub-site. This includes cases where the tumor's epicenter is unclear due to its extensive spread within the esophagus.
Apply this code when documentation clearly indicates a primary esophageal malignancy involving multiple adjacent anatomical regions of the esophagus (e.g., cervicothoracic, thoracoabdominal). This code is appropriate when the medical record explicitly states "overlapping sites" or describes a tumor spanning boundaries that prevent more specific sub-site assignment.
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