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Order Code BILAO Biliary Tract Malignancy, FISH, Varies


Specimen Required


Supplies: PreservCyt Vial (T536)

Specimen Type: Bile duct brushing, bile duct aspirate, hepatobiliary brushing, or hepatobiliary aspirate (fine-needle aspiration is not acceptable)

Container/Tube: Separate ThinPrep vial, containing 20 mL PreservCyt or CytoLyt solution for each specimen

Specimen Volume: Entire collection

Collection Instructions:

1. If performing local cytology in addition to fluorescence in situ hybridization testing, aliquot half of the specimen into another ThinPrep vial before processing the specimen.

2. Submission of residual specimen (after processing other testing) may compromise the sensitivity of the test.

3. Label each specimen with specific source (eg, right hepatic duct or common bile duct).


Useful For

Assessing bile duct brushing or hepatobiliary brushing specimens for biliary tract malignancy

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
BILOB Biliary Tract Malignancy, FISH No No
BILOC Biliary Tract Malignancy, FISH No No
BILOD Biliary Tract Malignancy, FISH No No
BILOE Biliary Tract Malignancy, FISH No No
BILOF Biliary Tract Malignancy, FISH No No

Testing Algorithm

When this test is ordered, fluorescence in situ hybridization testing will be performed. When additional specimens are received, the laboratory will add BILOB to the second specimen, BILOC to the third specimen, and so on.

Special Instructions

Method Name

Fluorescence In Situ Hybridization (FISH)

Reporting Name

Biliary Tract Malignancy, FISH

Specimen Type

Varies

Specimen Minimum Volume

See Specimen Required

Specimen Stability Information

Specimen Type Temperature Time Special Container
Varies Refrigerated (preferred)
  Ambient 

Reject Due To

Pancreatic mass
Pancreatic cyst
Pancreatic fine-needle aspiration (FNA)  		 Reject

Reference Values

No abnormality detected by fluorescence in situ hybridization

Method Description

Biliary cells are harvested, fixed, and placed on a slide. Fluorescently labeled DNA probes to 1q21 (MCL1), 7p12 (EGFR), 8q24 (MYC), and 9p21 (CDKN2A) (Abbott Molecular, Inc) are hybridized to the cells on the slide. The slide is then washed and stained with DAPI (4',6-diamidine-2'-phenylindole dihydrochloride, a nuclear counterstain). Fluorescence microscopy with unique band filters is used to assess 100 consecutive epithelial cells for gains and losses of probe signals (chromosomal loci). Specimens are considered abnormal if cell counts exceed predetermined cutoff values for one or more of the following abnormalities: polysomy, homozygous 9p21 loss, single locus gain, single locus gain with 9p21 loss in the same cells, and/or tetrasomy. If the cutoff for polysomy is not attained in the 100-cell enumeration, then the remainder of the slide is assessed for polysomy until the cutoff is reached or the slide is exhausted.(Unpublished Mayo method)

Day(s) Performed

Monday through Friday

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

88377