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IgG4, IHC with Interpretation
Test Code91315
CPT Codes
88342
Preferred Specimen
1 formalin-fixed, paraffin-embedded tissue block
Minimum Volume
1 Block
Other Acceptable Specimens
3 unstained, (+) charged slides, submitted in IHC Specimen Transport Kit
Instructions
Please include surgical pathology report.
Transport Container
IHC Specimen Transport Kit
Transport Temperature
Room temperature
Specimen Stability
Room temperature: Indefinite
Refrigerated: Indefinite
Frozen: Unacceptable
Refrigerated: Indefinite
Frozen: Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Received frozen
Methodology
Immunohistochemistry (IHC)
Setup Schedule
Setup: Mon-Fri a.m.; Report available: 3 days
Reference Range
See Laboratory Report
Clinical Significance
IgG4-related sclerosing disease is a clinicopathologically-defined immune disorder that can present in lymph node or other tissues. An increased number of IgG4+ plasma cells detected by this antibody can help establish the diagnosis, with cases showing histologic features of cutaneous pseudolymphomas and/or intra-germinal center and interfollicular plasmacytosis. Although the presence of increased numbers of IgG4+ plasma cells is not specific for this disease it can help differentiate it from inflammatory myofibroblastic tumor which typically shows absent or rare IgG4+ plasma cells.
Performing Laboratory
Quest Diagnostics Nichols Institute |
14225 Newbrook Drive |
Chantilly, VA 20153 |