Sign in →

Test ID NBLD0543 Renal Pathology Consultation, Wet Tissue

Useful For

Evaluating and managing patients with kidney disease

 

Following the progression of known kidney disease or response to therapy

 

Determining the cause of dysfunction in the transplanted kidney (allograft)

Specimen Type

Kidney Biopsy


Ordering Guidance


This test is for a renal wet tissue consultation only. For a consultation on paraffin embedded renal tissue and slides, order PATHC / Pathology Consultation.



Shipping Instructions


1. Advise shipping specimens in Styrofoam transportation coolers to avoid extreme hot or cold temperatures and to ensure specimens are received at required specimen transport (stability) temperature.

2. Attach the green "Attention Pathology" address label (T498) to the outside of the transport container before putting into the courier mailer.



Necessary Information


All requisition and supporting information must be submitted in English.

 

The following information is required:

1. All requisitions must be labeled with:

-Patient name, date of birth, and medical record number

-Name and phone number of the referring nephrologist/pathologist or ordering provider

-Anatomic site and collection date

 

2. A brief patient history is essential to achieve a consultation fully relevant to the ordering provider’s needs.

 

3. Additional information needed:

-Recent nephrology consultation notes

-History and physical progress notes

-Recent laboratory test results, including serologies (eg, renal/kidney function panel, antinuclear antibodies, anti-glomerular basement membrane antibodies, C3/C4, serum or urine protein electrophoresis, serum albumin, hepatitis/HIV screen, urinalysis)



Specimen Required


Specimen Type: Kidney biopsy

Supplies: Renal Biopsy Kit (T231)

Specimen Volume: Entire specimen

Collection Instructions: Collect and prepare biopsy specimens per instructions in Renal Biopsy Procedure for Handling Tissue for Light Microscopy, Immunofluorescent Histology, and Electron Microscopy.

Additional Information: On Saturdays and holidays, RUSH (same day as receipt) interpretation is available for clinically emergent cases (eg, acute kidney failure, rapidly progressive glomerulonephritis, acute kidney allograft dysfunction) but requires advanced notification and approval by a Mayo Clinic Renal Pathologist (507-284-5677).

To request RUSH service outside of regular business hours, contact Mayo Clinic Laboratories at 800-533-1710.


Specimen Minimum Volume

See Specimen Required

Reject Due To

All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Specimen Stability Information

Specimen Type Temperature Time Special Container
Kidney Biopsy Ambient (preferred)
  Refrigerated 

Day(s) Performed

Monday through Saturday

Report Available

2 to 10 days; Cases requiring additional material or ancillary testing may require additional time.

Method Name

Pathology Consultation

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

88305 (If appropriate)

88348 (If appropriate)

88313 (If appropriate)

88346 (If appropriate)

88350 (If appropriate)

Forms

1. Renal Biopsy Patient Information

2. If not ordering electronically, complete, print, and send a Renal Diagnostics Test Request (T830) with the specimen.

Secondary ID

70591

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
EMR EM, Renal Biopsy No, (Bill Only) No
IFPCA IF Additional No, (Bill Only) No
IFPCI IF Initial No, (Bill Only) No
LV4RP Level 4 Gross and Microscopic, RB No, (Bill Only) No
SS2PC SpecStain, Grp II, other No, (Bill Only) No

Testing Algorithm

The Renal Pathology Consultation is performed by a Mayo Clinic renal pathologist and entails the performance of appropriate procedures and stains based on the material received, patient information, and specific findings on the case in order to determine a diagnosis. Optimal/standard diagnostic interpretation of a medical kidney biopsy requires integration of the light microscopy, immunofluorescence, and electron microscopy findings together with the clinical and laboratory data for the patient. Published standards by the Renal Pathology Society are followed for the diagnostic evaluation and reporting of non-neoplastic kidney disease.(1)

 

Light Microscopy:

Wet/unprocessed tissue submitted for light microscopy routinely includes the preparation of stains, which include hematoxylin and eosin, periodic acid Schiff, Masson trichrome, and Jones methenamine silver stains.

 

Immunofluorescence:

Wet/unprocessed tissue submitted for immunofluorescence may include the following stains to render an accurate diagnosis. These stains include IgA, IgG, IgM, C1q, C3, albumin, fibrinogen, kappa light chain, and lambda light chain stains with C4d added if the biopsy is an allograft.

 

The IgG subtypes (IgG1, IgG2, IgG3, IgG4) are typically only utilized if the biopsy shows features suspicious for a monoclonal/monotypic deposition process involving IgG.

 

Alport (collagen IV, alpha 2 and alpha 5) staining is performed in the setting of biopsy findings that are consistent with hereditary nephritis/Alport syndrome.

 

Phospholipase A2 receptor staining is performed in the setting of membranous nephropathy/glomerulonephritis to aid in determining whether it is most likely primary/idiopathic or secondary.

 

Paraffin-Based Immunofluorescence Stains:

The paraffin-based immunofluorescence stains listed above would only be utilized in the special circumstance when there is no tissue or inadequate tissue available for standard immunofluorescence or if there are findings that raise concern for so-called "masked deposits."

 

Electron Microscopy:

Wet/unprocessed tissue submitted for electron microscopy will be processed for transmission electron microscopy. A formal interpretive report is issued, incorporating the findings from all tests performed for diagnostic purposes.

 

For more information see Pathology Consultation Ordering Algorithm.

Reporting Name

Renal Pathology

Reference Values

Results of the consultation are reported in a formal pathology report, which may include a description of ancillary test results (if applicable) and an interpretive comment.

Test Classification

Not Applicable
Sanford Laboratories - Fargo Additional Information:

SANFORD INTERFACE BUILD INFORMATION

Result Code Result Code Description
22116 Interpretation
22117 Participated in the Interpretation
22118 Report Electronically Signed By
22119 Addendum
22120 Gross Description
22121 Material Received
22122 Disclaimer
22123 Case Number