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Test ID KIPM Ki-67(MIB-1), Pulmonary, Quantitative Immunohistochemistry, Manual


Shipping Instructions


Attach the green pathology address label included in the kit to the outside of the transport container.



Necessary Information


1. Pathologist's name, address, and phone number are required.

2. Include accompanying pathology report stating the final diagnosis. If not available, a preliminary diagnosis is acceptable.



Specimen Required


Only orderable as a reflex. For more information see KI67P / Ki-67 (MIB-1), Pulmonary, Quantitative Immunohistochemistry, Automated.

 

Supplies: Pathology Packaging Kit (T554)

Specimen Type:

Preferred: Formalin-fixed, paraffin-embedded tissue block containing carcinoid/atypical carcinoid of the lung including metastases.

Acceptable: 2 Unstained sections on charged slides cut at 4 microns <1 month ago. Tissue on the slides should have been fixed in 10% neutral buffered formalin.

Container/Tube: Pathology Packaging Kit

Collection Instructions:

1. Submit formalin-fixed, paraffin-embedded tissue block.

2. Attach the green pathology address label included in the kit to the outside of the transport container.

Additional Information: Paraffin block will be returned with the final report.


Useful For

Determining proliferation of tumor cells in paraffin-embedded tissue blocks from patients diagnosed with carcinoid or atypical carcinoid of the lung including metastases, using a manual method

Method Name

Only orderable as a reflex. For more information see KI67P / Ki-67 (MIB-1), Pulmonary, Quantitative Immunohistochemistry, Automated.

 

Immunohistochemistry, Semi- Quantitation, Hot-Spot Technique

Reporting Name

Ki67 Pulmonary IHC Manual

Specimen Type

Special

Specimen Stability Information

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

Reference Values

Only orderable as a reflex. For more information see KI67P / Ki-67 (MIB-1), Pulmonary, Quantitative Immunohistochemistry, Automated.

 

Varies by tumor type; values reported from 0% to 100%

Day(s) Performed

Monday through Friday

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

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

CPT Code Information

88360

LOINC Code Information

Test ID Test Order Name Order LOINC Value
KIPM Ki67 Pulmonary IHC Manual In Process

 

Result ID Test Result Name Result LOINC Value
72138 Interpretation 29593-1
72139 Participated in the Interpretation No LOINC Needed
72140 Report electronically signed by 19139-5
72141 Material Received 81178-6
72142 Disclaimer 62364-5
72143 Case Number 80398-1

NY State Approved

Yes