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Test ID THSIF Thrombospondin Type 1 Domain Containing 7A (THSD7A), Immunofluorescence


Ordering Guidance


If additional interpretation/analysis is needed, request PATHC / Pathology Consultation along with this test and send the corresponding renal pathology light microscopy and immunofluorescence (IF) slides (or IF images on a CD), electron microscopy images (prints or CD), and the pathology report.

Necessary Information


A preliminary pathology report is required for testing to be performed. Send information with specimen. The laboratory will not reject testing if a reason for testing is not provided; however appropriate testing and interpretation may be compromised or delayed. If not provided, an appropriate indication for testing may be entered by Mayo Clinic Laboratories.



Specimen Required


Specimen Type: Kidney tissue

Preferred: 2 Unstained positively charged glass slide (25- x 75- x 1-mm) per test ordered; paraffin sections 3 to 4-microns thick

Acceptable: Formalin-fixed, paraffin-embedded (FFPE) kidney tissue block


Reporting Name

THSD7A Immunofluorescence

Specimen Type

Special

Specimen Stability Information

Specimen Type Temperature Time
Special Ambient (preferred)
  Frozen 
  Refrigerated 

Report Available

1 to 2 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

LOINC Code Information

Test ID Test Order Name Order LOINC Value
THSIF THSD7A Immunofluorescence 101116-2

 

Result ID Test Result Name Result LOINC Value
605245 Interpretation 50595-8
606383 Participated in the Interpretation No LOINC Needed
606384 Report electronically signed by 19139-5
606385 Addendum 35265-8
606386 Gross Description 22634-0
606387 Material Received 22633-2
606388 Disclaimer 62364-5
606389 Case Number 80398-1

Forms

If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:

-Kidney Transplant Test Request

-Renal Diagnostics Test Request (T830)

Useful For

Diagnosis of thrombospondin type 1 domain-containing 7A (THSD7A)-associated membranous nephropathy

Day(s) Performed

Monday through Friday

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

88346-Primary IF

88350-If additional IF

Specimen Minimum Volume

See Specimen Required

Method Name

Direct Immunofluorescence (DIF)