Malignant carcinoid tumor: Difference between revisions

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{{ICD10 transition status

| OldDxArticle =

| CurrentStatus = ~~freshly automatically generated article~~

| CurrentStatus = reconciled

| InitialEditorAssigned = Debbie Page-Newton

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~~{{ICD10 category|Neuro}}~~{{ICD10 category|Neoplastic}}

== Additional Info ==

*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.

**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]]

== ~~Additional Info ==~~

~~located anywhere~~; also code ~~Carcinoid syndrome if present~~

{{ICD10 nonstandard code

| exception_type = CA

| 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.

}}

== Alternate ICD10s to consider coding instead or in addition ==

~~(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)~~

* [[Carcinoid syndrome]]

== Candidate [[Combined ICD10 codes]] ==

== ~~Candidate [[Combined ICD10 codes]]~~ ==

== Related CCI Codes ==

~~(put links to likely candidates coded with this one, eg. a cause for a trauma.)~~

~~== Related CCI Codes ==~~

== Related Articles ==

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 {{ICD10 transition status
 | OldDxArticle =
-| CurrentStatus = freshly automatically generated article
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Debbie Page-Newton
 }}
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 | BugRequired=
 }}
-{{ICD10 category|Neuro}}{{ICD10 category|Neoplastic}}
+{{ICD10 category|Neoplastic}}
+== Additional Info ==
+*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.
+**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]]
-== Additional Info ==
-located anywhere; also code Carcinoid syndrome if present
+{{ICD10 nonstandard code
+| exception_type = CA
+| 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.
+}}
+{{ICD10 Guideline Cancer}}
 == Alternate ICD10s to consider coding instead or in addition ==
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+* [[Carcinoid syndrome]]
+== Candidate [[Combined ICD10 codes]] ==
-== Candidate [[Combined ICD10 codes]] ==
+== Related CCI Codes ==
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
-== Related  CCI Codes ==
+{{Data Integrity Check List}}
 == Related Articles ==
 {{Related Articles}}
 {{ICD10 footer}}
 {{EndPlaceHolder}}