Progressive Multifocal Leukoencephalopathy (PML): Difference between revisions
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{{ICD10 dx | |||
|ICD10 Code=A81.2 | |||
}} | |||
{{ICD10 category|Infectious disease}} | |||
{{ICD10 category|Neuro}} | |||
{{ICD10 category|Virus}} | |||
{{ICD10 category|Potential infection}} | |||
{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =| CurrentStatus = | | OldDxArticle =Neurologic Other | ||
| CurrentStatus = reconciled | |||
| InitialEditorAssigned = Allyson Alcudia | | InitialEditorAssigned = Allyson Alcudia | ||
}} | }} | ||
== Additional Info == | == Additional Info == | ||
*PML is a rare and often fatal neurologic disease marked by progressive, immune-mediated, multifocal damage to the white matter of the brain. | |||
* also known as vanishing white matter disease (VWM) | |||
*Most cases are caused by JC virus, however, an increasing other cause is new immune-modifying drugs. | |||
== Alternate ICD10s to consider coding instead or in addition == | |||
== | == Candidate [[Combined ICD10 codes]] == | ||
{{ICD10 Guideline Infection}} | |||
== Related CCI Codes == | |||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | |||
{{ICD10 footer}} | |||
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