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| Paraneoplastic Autoantibody Evaluation | ||
| Order Code: PNSER
Order Form: A-1a Miscellaneous Request or IPR Req |
Commercial "Mail-out" Laboratory 6240 RCP 356-3527 |
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Specimen |
Serum | |||||
Collection Medium: |
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Minimum: |
Adult minimum: 12 mls whole blood in two 6 ml red top tubes to yield (min: 4.0 mL serum) Pediatric minimum: 6 mls whole blood in one red top tube to yield (min: 2.0 mL serum) | |||||
Analytic Time: |
2 weeks | |||||
Reference Range: |
NEURONAL NUCLEAR ANTIBODIES Antineuronal Nuclear Antibody-Type 1 (ANNA-1) Negative at <1:240 Antineuronal Nuclear Antibody-Type 2 (ANNA-2) Negative at <1:240 Antineuronal Nuclear Antibody-Type 3 (ANNA-3) Negative at <1:240 NEURONAL AND MUSCLE CYTOPLASMIC ANTIBODIES Purkinje Cell Cytoplasmic Antibody, Type 1 (PCA-1) Negative at <1:240 Purkinje Cell Cytoplasmic Antibody, Type 2 (PCA-2) Negative at <1:240 Purkinje Cell Cytoplasmic Antibody, Type Tr (PCA-Tr) Negartive at <1:240 Amphiphysin Antibody Negative at <1:240 CRMP-5-IgG Negative at <1:240 Note: Titers lower than 1:240 are detectable by recombinant CRMP-5 Western blot analysis. CRMP-5 Western blot analysis will be done on request on stored serum (held 4 weeks). This supplemental testing is recommended in cases of chorea, vision loss, cranial neuropathy, and myelopathy. Call the Clinical Pathology Core Laboratory at 356-3527 to request CRMP-5 Western blot. Striational (Striated Muscle) Antibodies Negative at <1:60 CATION CHANNEL ANTIBODIES N-Type Calcium Channel Antibody < or = 0.03 nmol/L P/Q-Type Calcium Channel Antibody < or = 0.02 nmol/L ACh Receptor (Muscle) Binding Antibody < or = 0.02 nmol/L AChR Ganglionic Neuronal Antibody < or = 0.02 nmol/L Neuron-restricted patterns of IgG staining that do not fulfill criteria for amphiphysin, ANNA-1, ANNA-2, ANNA-3, PCA-1, PCA-2, PCA-Tr, or CRMP-5-IgG may be reported as "unclassified antineuronal IgG." Complex patterns that include non-neuronal elements may be reported as "uninterpretable." VGKC-Antibody: Neuronal voltage-gated potassium channel Less than or equal to 0.02 nmol/L | |||||
Comments: |
If IFA are indeterminate, paraneoplastic autoantibody Western blot is performed. If requested or if IFA suggests CRMP-5-IgG, CRMP-5-IgG Western blot is performed. If calcium channel P/Q-Type or N-Type is >20, paraneoplastic auto-antibody Western blot and CRMP-5-IgG Western blot are performed. If IFA suggests GAD65 antibody, GAD65 antibody radioimmuno-preciptation assay is performed. If ACh receptor binding antibody is >0.02 or if striational antibodies is >= 1:60, ACh receptor modulating antibodies, paraneoplastic autoantibody Western blot, and CRMP-5-IgG Western blot are performed. If ACh receptor modulating antibodies antibody is >= 40% loss, ACh receptor blocking antibodies radioimmunoassay is performed. CRMP-5-IgG Western blot is also performed by specific request for more sensitive detection of CRMP-5-IgG. Testing should be requested in cases of subacute basal ganglionic disorders (chorea, Parkinsonism), cranial neuropathies (especially loss of vision, taste or smell) and myelopathies. | |||||
Methodology: |
Indirect Immunofluorescence (IFA) Enzyme Immunoassay (EIA) Radioimmunoassay (RIA) Western Blot | |||||
CPT Code: |
83519 modifier 59 ACh Receptor (muscle) binding antibody
83519 modifier 59 AChR Ganglionic neuronal antibody
83519 modifier 59 N-type Calcium channel antibody
83519 modifier 59 P/Q-type Calcium channel antibody
83520 Striational (striated muscle) antibodies
86256 AGNA
86256 Amphiphysin
86256 ANNA-1
86256 ANNA-2
86256 ANNA-3
86256 CRMP-5-IgG
86256 PCA-1
86256 PCA-2
86256 PCA-Tr
83519 modifier 59 ACh receptor (muscle) blocking antibodies (if
appropriate)
83519 modifier 59 ACh receptor (muscle) modulating antibodies (if
appropriate)
84182 CRMP-5-IgG Western blot (if appropriate)
84182 Paraneoplastic autoantibody Western blot confirmation (if
appropriate)
86341 GAD65 antibody assay (if appropriate)
83519 VGKC-Antibody | |||||
See also: Paraneoplastic Autoantibody Evaluation, CSF |
Updated: 06/30/2008
Note: The information contained in this handbook is for use by personnel of University of Iowa Health Care. No other use is implied or intended.