Test ID FGENC Fungal Culture, Spinal Fluid
Useful For
Diagnosing fungal infections from cerebrospinal fluid (separate tests are available for other specimen sites)
Method Name
Conventional agar culture technique with identification by macroscopy and microscopic morphology, nucleic acid hybridization probes, D2 rDNA gene sequencing, real-time polymerase chain reaction (rtPCR), or MALDI-TOF mass spectrometry. Dimorphic pathogen identification is confirmed using molecular methods (ie, D2 rDNA gene sequencing, rtPCR or MALDI-TOF mass spectrometry).
(PCR is utilized pursuant to a license agreement with Roche Molecular Systems, Inc.)
Reporting Name
Fungal Culture, CSFSpecimen Type
CSFOnly orderable as a reflex. For more information see LFACX / Crytpococcus Antigen with Reflex, LFA, Spinal Fluid.
Specimen should arrive within 24 hours of collection.
Specimen Type: Spinal fluid
Container/Tube: Sterile vial
Specimen Volume: 1 mL
Specimen Minimum Volume
0.1 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
CSF | Refrigerated (preferred) | 14 days |
Ambient | 14 days | |
Frozen | 14 days |
Clinical Information
Many fungi in the environment cause disease in severely compromised human hosts. Accordingly, the range of potential pathogenic fungi has increased as the number of immunosuppressed individuals (eg, persons with AIDS, patients receiving chemotherapy, or transplant rejection therapy) has increased.
Few fungal diseases can be diagnosed clinically; many are diagnosed by isolating and identifying the infecting fungus in the clinical laboratory.
Reference Values
Negative
If positive, fungus will be identified.
Cautions
For optimal recovery of organisms, sufficient specimen should be transported within 24 hours of collection.
Fungi can be pathogens, colonizers, or contaminants. Correlation of the patient clinical condition with culture results is necessary for optimal patient care.
Day(s) Performed
Monday through Sunday; Continuously
Report Available
24 days/Positive cultures reported when detected. Preliminary negative report generated at 7 and 14 days.Performing Laboratory

Test Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
87102-Fungal culture, routine
87106-Yeast identification panel C (if appropriate)
87106-Yeast identification panel D (if appropriate)
87106-Id MALDI-TOF Mass Spec Yeast (if appropriate)
87107-Id MALDI-TOF Mass Spec Fungi (if appropriate)
87107-Fungal identification panel A (if appropriate)
87107-Fungal identification panel B (if appropriate)
87107-Yeast identification panel A (if appropriate)
87107-Yeast identification panel B (if appropriate)
87150-Identification rapid PCR Coccidioides (if appropriate)
87150 x 2-Identification Histoplasma/Blastomyces, PCR (if appropriate)
87150-Microbial probe, fungus identification (if appropriate)
87153-D2 fungal sequencing identification (if appropriate)
87176-Tissue processing (if appropriate)