Summary & Overview
HCPCS M1193: Surgical Pathology Report for MMR/MSI Testing
HCPCS Level II code M1193 denotes surgical pathology reports that include an impression or conclusion about mismatch repair (MMR) status by immunohistochemistry, microsatellite instability (MSI) status by DNA-based testing, or a recommendation to perform those tests. This code is important nationally as MMR and MSI testing guide cancer diagnosis, prognostication, and therapy selection, including immunotherapy decisions and hereditary cancer evaluations. Payers commonly engaged in coverage and reimbursement for these pathology services include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare.
Readers will find a concise overview of the clinical context for reporting MMR and MSI results, typical service settings, and which payers are relevant for coverage considerations. The publication summarizes coding use and documentation expectations for surgical pathology reports, presents payer coverage scope, and highlights how MMR/MSI status is positioned within diagnostic workflows and downstream care decisions. Data not available in the input will be identified as such where relevant.
Billing Code Overview
HCPCS Level II code M1193 describes surgical pathology reports that contain an impression or conclusion of, or a recommendation for testing of, MMR by immunohistochemistry, MSI by DNA-based testing status, or both. This code applies to pathology documentation that communicates results or advises molecular testing for mismatch repair (MMR) protein expression via immunohistochemistry and/or microsatellite instability (MSI) status determined by DNA-based methods.
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Service type: Pathology consultation and diagnostic reporting that interprets tumor testing for MMR and/or MSI status
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Typical site of service: Hospital pathology laboratories, independent pathology labs, and outpatient surgical pathology services
Clinical & Coding Specifications
Clinical Context
A 62-year-old patient undergoes surgical resection of a colorectal mass. The surgical pathology specimen is processed and the final pathology report includes a diagnostic impression recommending or reporting testing for mismatch repair (MMR) protein expression by immunohistochemistry (IHC) and/or microsatellite instability (MSI) status by DNA-based testing. This service typically occurs after grossing, histologic review, and pathologist interpretation of hematoxylin and eosin slides when features suggest possible Lynch syndrome, sporadic MMR deficiency, or when tumor features (e.g., high-grade histology, tumor-infiltrating lymphocytes, mucinous features) prompt reflex biomarker testing.
Workflow steps:
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Specimen accessioning and gross description by pathology staff.
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Tissue processing, embedding, sectioning, and H&E slide review by pathologist.
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Pathologist documents impression recommending or ordering
MMRtesting by IHC,MSItesting by DNA-based methods, or both in the surgical pathology report. -
If performed, laboratory runs IHC for MLH1, MSH2, MSH6, PMS2 and/or PCR/NGS-based MSI panel; results are incorporated into the final report or issued as an addendum.
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Final report containing the impression and MMR/MSI test results is released to the surgical team and the ordering clinician for treatment planning and genetic counseling as indicated.
Typical site of service: hospital outpatient pathology/laboratory, hospital inpatient pathology, independent reference laboratory, or integrated academic pathology department.
Typical patient scenario: adult with colorectal carcinoma, endometrial carcinoma, or other tumors where MMR deficiency impacts prognosis, immunotherapy eligibility, and hereditary cancer evaluation.