Paraneoplastic Antibody Expanded Evaluation w/Reflex to Titer and LB, Serum

Paraneoplastic Antibody Expanded Evaluation w/Reflex to Titer and LB, Serum

Test Code

94957
86255 (x19), 86052, 83519 (x2), 86596 (x2), 86341
94957
86255 (x19), 86052, 83519 (x2), 86596 (x2), 86341
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection is not available in your area through Quest Mobile.

Clinical Significance

Paraneoplastic Antibody Expanded Evaluation w/Reflex to Titer and LB, Serum - Detection of antineuronal autoantibodies aids the diagnosis of autoimmune paraneoplastic syndromes, encephalopathies, and other autoimmune neurological conditions. Identification of specific antineuronal autoantibodies may also help in the diagnostic workup for occult malignancies. Finally, knowledge of the specific identity of antineuronal autoantibodies aids greatly in making therapeutic decisions for patients. Antineuronal antibodies are detected and identified by indirect immunofluorescence, using multiple neuronal tissues, non-neuronal tissues, and transfected substrate cells, as well as radioimmunoassays. Line blot assays are used for confirmatory reflex testing.

Test Details

Includes

  • Initial panel consits of:Paraneoplastic Expanded Ab Screen Tissue IFA, AMPAR1, AMPAR2, Aquaporin 4, DPPX, GABAbR, NMDAR1, CASPAR2, LGI1, Ganglionic AChR, VGCC N-Type, VGCC P/Q type and VGKC

    If Paraneoplastic Expanded Ab Screen, Tissue IFA suggests one or more positive analytes, a line blot with 10 analytes will be performed: ANNA1 (Hu), ANNA2 (Ri), PCA1 (Yo), Ma2/Ta, CRMP5(CV2), Amphiphysin, AGNA1 (SOX1), GAD65, PCA Tr (DNER), and Zic4.

    If the Paraneoplastic Expanded Ab Screen, Tissue IFA suggests ANNA3, then titer will be performed.
    If the Paraneoplastic Expanded Ab Screen, Tissue IFA suggests PCA-2, then titer will be performed.

    If the Paraneoplastic Expanded Ab Screen, Tissue IFA suggests PCA-Tr (DNER) and Neurology Antibody Line Blot shows PCA Tr (DNER) negative and PCA1 (Yo) negative, then Purkinje Cell Cytoplasmic Antibody Type Tr (DNER), CBA, IFA will be performed at an additional charge (CPT code(s): 86255).
    ⁠⁠⁠⁠⁠⁠⁠If Purkinje Cell Cytoplasmic Antibody Type Tr (DNER), CBA, IFA is positive, then titer will be performed.

    If the Paraneoplastic Expanded Ab Screen, Tissue IFA for Myelin antibody is positive, then:
    a. Myelin antibody IFA titer will be performed at an additional charge (CPT code(s): 86256).
    b. Myelin Associated Glycoprotein (MAG) Antibody Western Blot will be performed at an additional charge (CPT code(s): 84182)
    c. If Myelin Associated Glycoprotein (MAG) Antibody Western Blot is positive, then Myelin Associated Glycoprotein (MAG)-SGPG Antibody and Myelin Associated Glycoprotein (MAG) Antibody (IgM) EIA will be performed at an additional charge (CPT code(s): 83520 x2).

    If the Neurology Antibody, CBA is positive for NMDAR1, AMPAR2, LGI-1, or CASPR2, then titers will be performed at an additional charge (CPT code(s): 86256 for each titer performed).

    If the Aquaporin 4 (AQP4) Ab, CBA is positive, then titer will be performed at an additional charge (CPT code(s): 86052).

    If the Neurology Antibody, CBA is positive for AMPAR1 or GABA-B Receptor, then titers will be performed.

    If the DPPX Receptor Antibody, CBA is positive, then titer will be performed.

Methodology

See individual tests

Assay Category

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

See Laboratory Report

Alternative Name(s)

Autoimmune Paraneoplastic Panel Reflex, Paraneoplastic Autoimmune Evaluation, PNS Expanded, Para Expanded Serum

LOINC® Codes, Performing Laboratory

Initial panel consits of:Paraneoplastic Expanded Ab Screen Tissue IFA, AMPAR1, AMPAR2, Aquaporin 4, DPPX, GABAbR, NMDAR1, CASPAR2, LGI1, Ganglionic AChR, VGCC N-Type, VGCC P/Q type and VGKC

If Paraneoplastic Expanded Ab Screen, Tissue IFA suggests one or more positive analytes, a line blot with 10 analytes will be performed: ANNA1 (Hu), ANNA2 (Ri), PCA1 (Yo), Ma2/Ta, CRMP5(CV2), Amphiphysin, AGNA1 (SOX1), GAD65, PCA Tr (DNER), and Zic4.

If the Paraneoplastic Expanded Ab Screen, Tissue IFA suggests ANNA3, then titer will be performed.
If the Paraneoplastic Expanded Ab Screen, Tissue IFA suggests PCA-2, then titer will be performed.

If the Paraneoplastic Expanded Ab Screen, Tissue IFA suggests PCA-Tr (DNER) and Neurology Antibody Line Blot shows PCA Tr (DNER) negative and PCA1 (Yo) negative, then Purkinje Cell Cytoplasmic Antibody Type Tr (DNER), CBA, IFA will be performed at an additional charge (CPT code(s): 86255).
⁠⁠⁠⁠⁠⁠⁠If Purkinje Cell Cytoplasmic Antibody Type Tr (DNER), CBA, IFA is positive, then titer will be performed.

If the Paraneoplastic Expanded Ab Screen, Tissue IFA for Myelin antibody is positive, then:
a. Myelin antibody IFA titer will be performed at an additional charge (CPT code(s): 86256).
b. Myelin Associated Glycoprotein (MAG) Antibody Western Blot will be performed at an additional charge (CPT code(s): 84182)
c. If Myelin Associated Glycoprotein (MAG) Antibody Western Blot is positive, then Myelin Associated Glycoprotein (MAG)-SGPG Antibody and Myelin Associated Glycoprotein (MAG) Antibody (IgM) EIA will be performed at an additional charge (CPT code(s): 83520 x2).

If the Neurology Antibody, CBA is positive for NMDAR1, AMPAR2, LGI-1, or CASPR2, then titers will be performed at an additional charge (CPT code(s): 86256 for each titer performed).

If the Aquaporin 4 (AQP4) Ab, CBA is positive, then titer will be performed at an additional charge (CPT code(s): 86052).

If the Neurology Antibody, CBA is positive for AMPAR1 or GABA-B Receptor, then titers will be performed.

If the DPPX Receptor Antibody, CBA is positive, then titer will be performed.

Methodology

See individual tests
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

See Laboratory Report

Alternative Name(s)

Autoimmune Paraneoplastic Panel Reflex, Paraneoplastic Autoimmune Evaluation, PNS Expanded, Para Expanded Serum

Preferred Specimen(s)

8 mL frozen serum

Minimum Volume

4 mL

Transport Container

Transport tube

Transport Temperature

Frozen

Specimen Stability

  • Room temperature: 24 hours
  • Refrigerated: 48 hours
  • Frozen: 21 days

Reject Criteria

Gross hemolysis • Lipemia • Received refrigerated • Received room temperature • Freeze/thaw >3 cycles

Setup Schedule

8 mL frozen serum
4 mL
Transport tube
Frozen
Room temperature: 24 hours
Refrigerated: 48 hours
Frozen: 21 days
Gross hemolysis • Lipemia • Received refrigerated • Received room temperature • Freeze/thaw >3 cycles
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection is not available in your area through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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