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Test Code RPCWT Renal Pathology Consultation, Wet Tissue


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.


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)

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.

Method Name

Pathology Consultation

Reporting Name

Renal Pathology

Specimen Type

Kidney Biopsy

Specimen Minimum Volume

See Specimen Required

Specimen Stability Information

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

Reject Due To

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

Clinical Information

The Mayo Renal Pathology service is staffed by board-certified pathologists who have a special interest in non-neoplastic diseases of the kidney.

 

Kidney biopsy has proven to be of value in the clinical evaluation and management of patients with kidney disease, including acute and chronic renal insufficiency, nephrotic syndrome, nephritic syndrome, proteinuria, and hematuria, and in the overall management of kidney transplant recipients.

 

Optimal interpretation of a kidney biopsy requires integration of clinical and laboratory results with light microscopic, immunofluorescent histology, and electron microscopy findings.

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.

Interpretation

Both a verbal report and a faxed report are provided to nephrologists for Mayo Clinic Laboratories cases.

 

Digital images for electron microscopy and immunofluorescent stains may be downloaded as needed using the digital imaging link provided in the final report.

 

In most cases, electron microscopy results are reported as an addendum, and a final report including these findings is issued. This final report is again faxed to the submitting nephrologist and mailed to the submitting pathology laboratory, along with a representative set of the light microscopy slides.

Cautions

Accurate and timely interpretation of a kidney biopsy requires integration of light microscopic, immunofluorescent histology, and electron microscopic findings with clinical and laboratory data. Failure to provide the relevant clinical history and laboratory results may result in a delay in the interpretation or the inability to adequately correlate the biopsy findings with the clinical picture.

Method Description

Gross and microscopic examination of tissue. Ancillary testing is ordered at the discretion of the Mayo Clinic pathologist. The results of all testing will be provided in the context of the final pathology report.(Unpublished Mayo method)

Day(s) Performed

Monday through Saturday

Report Available

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

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)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
RPCWT Renal Pathology 65757-7

 

Result ID Test Result Name Result LOINC Value
71219 Interpretation 60570-9
71220 Participated in the Interpretation No LOINC Needed
71221 Report electronically signed by 19139-5
71222 Addendum 35265-8
71223 Gross Description 22634-0
71224 Material Received 85298-8
71615 Disclaimer 62364-5
71846 Case Number 80398-1

Test Classification

Not Applicable