Malignant carcinoid tumor: Difference between revisions
Ttenbergen (talk | contribs) m Text replacement - "== Alternate ICD10s to consider coding instead or in addition ==" to "{{ICD10 Guideline Cancer}} == Alternate ICD10s to consider coding instead or in addition ==" |
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| explanation = there is no Canadian code for carcinoid tumor and so we used this US code; this is also the reason why this code has a letter in it. | | explanation = there is no Canadian code for carcinoid tumor and so we used this US code; this is also the reason why this code has a letter in it. | ||
}} | }} | ||
*Carcinoid tumors are of neuroendocrine origin. They are usually slow-growing. They may secrete one or another substance that leads to a variety of symptoms, of which the most common is [[Carcinoid syndrome]]. But not all carcinoids secrete. Also, carcinoid tumors may be malignant (this code) or benign. They can arise in any organ, though the GI tract is the most common source. | |||
*This is for a carcincoid located anywhere; also code [[Carcinoid syndrome]] if present | **As of January 2021 we have not included a specific code for benign carcinoid tumors --- to code one use the appropriate benign neoplasm code and IF the person also has [[Carcinoid syndrome]], link it to that code. | ||
*This code is for a carcincoid located anywhere; also code [[Carcinoid syndrome]] if present | |||
* | *IF it is known, you can link this code with the origin of the carcinoid tumor --- e.g. if it is a carcinoid originating in the lung, link this code with [[Lung and/or bronchus, primary malignancy]] | ||
{{ICD10 Guideline Cancer}} | {{ICD10 Guideline Cancer}} | ||