Test Code LAB20001-FNA Fine Needle Aspirate Cytology - Liquid Based (Non-Gyn)
Department
CYTOLOGY
Collection Requirements
FNA specimens may be collected in a container of Cytorich Red, a fixative specifically indicated for use with automated technology. Specimen maybe ejected from needle hub directly into the properly labeled container of fixative solution and sent with accompanying requisition to cytology. If lymphoma is suspected or if the FNA is of a lymph node, submit additional specimen in a container of RPMI solution for flow cytometry studies if warranted.
GENERAL REQUIREMENTS:
All cytology specimens submitted for testing should have the following information included on the requisition. Vials must be clearly labeled with patient identifier and contain collection device. Specimens accepted only from physician’s or designee.
-Patient Name
-Date of Birth
-Date of Specimen Collection
-Source of Cytologic Material
-Submitting Clinician’s Name
-MRN
-Pertinent Clinical Information
-Diagnosis Code
Primary Collection Container
Cytorich-Red (Autocyte Red)
Transport
Ambient
Stability
Refrigerate residual specimen, if applicable, until final report issued.
Minimum Testing Volume
5 mL (including fixative)
Reference Range
By report
Methodology
SurePath Prep Stain Processor
Performed
Monday – Friday
Reported
Varies
CPT Codes
88112
Unacceptable Conditions
Any of the above listed conditions under general requirements is omitted. Specimen received without patient identifier on container. Name on container does not match name on requisition. Excessive container leakage.