Back to HomeBeta

ICD-10 Coding for Pancreatic Neuroendocrine Tumor(C25.4, C7A.094)

Complete ICD-10-CM coding and documentation guide for Pancreatic Neuroendocrine Tumor. Includes clinical validation requirements, documentation requirements, and coding pitfalls.

Also known as:

PNETIslet Cell TumorPancreatic NETpancreatic carcinoid

Related ICD-10 Code Ranges

Complete code families applicable to Pancreatic Neuroendocrine Tumor

C25.0-C25.9Primary Range

Malignant neoplasm of pancreas

Primary range for pancreatic neuroendocrine tumors, specifying site-specific malignancies.

Malignant neuroendocrine tumor of foregut

Used for foregut neuroendocrine tumors when pancreatic origin is not confirmed.

Code Comparison: When to Use Each Code

Compare key differences between these codes to ensure accurate selection

CodeDescriptionWhen to UseKey Documentation
C25.4Malignant neoplasm of endocrine pancreasUse for nonfunctional pancreatic neuroendocrine tumors with confirmed pancreatic origin.
  • Nonfunctional tumors, incidental findings on imaging, elevated chromogranin A/synaptophysin
C7A.094Malignant neuroendocrine tumor of foregutUse for foregut neuroendocrine tumors when pancreatic origin is not confirmed.
  • Tumor involves foregut structures, pancreatic origin not confirmed.

Clinical Decision Support

Always review the patient's clinical documentation thoroughly. When in doubt, choose the more specific code and ensure documentation supports it.

Key Information: ICD-10 code for pancreatic neuroendocrine tumor

Essential facts and insights about Pancreatic Neuroendocrine Tumor

The ICD-10 code for a pancreatic neuroendocrine tumor is C25.4 for nonfunctional tumors with confirmed pancreatic origin.

Primary ICD-10-CM Codes for pancreatic neuroendocrine tumor

Malignant neoplasm of endocrine pancreas
Billable Code

Decision Criteria

clinical Criteria

  • Nonfunctional tumor with confirmed pancreatic origin.

Applicable To

  • Nonfunctional pancreatic neuroendocrine tumors

Excludes

  • Functional pancreatic neuroendocrine tumors

Clinical Validation Requirements

  • Nonfunctional tumors, incidental findings on imaging, elevated chromogranin A/synaptophysin

Code-Specific Risks

  • Incorrectly coding functional tumors under this code.

Coding Notes

  • Ensure documentation specifies nonfunctional status and pancreatic origin.

Ancillary Codes

Additional codes that should be used in conjunction with the main diagnosis codes when applicable.

Carcinoid syndrome

E34.0
Use when carcinoid syndrome is present alongside the primary tumor.

Differential Codes

Alternative codes to consider when ruling out similar conditions to the primary diagnosis.

Malignant neuroendocrine tumor of foregut

C7A.094
Use when tumor involves foregut structures and pancreatic origin cannot be confirmed.

Malignant neoplasm of endocrine pancreas

C25.4
Use for confirmed pancreatic origin tumors.

Documentation & Coding Risks

Avoid these common documentation and coding issues when documenting Pancreatic Neuroendocrine Tumor to ensure proper reimbursement, maintain compliance, and reduce audit risk. These guidelines are particularly important when using ICD-10 code C25.4.

Impact

Clinical: Impacts treatment decisions and prognosis., Regulatory: Non-compliance with documentation standards., Financial: Potential for denied claims due to insufficient documentation.

Mitigation Strategy

Ensure pathology reports include tumor grade and Ki-67 index., Educate staff on documentation standards.

Impact

Reimbursement: Incorrect coding can lead to denied claims., Compliance: Non-compliance with coding guidelines., Data Quality: Inaccurate clinical data reporting.

Mitigation Strategy

Use C25.4 for pancreatic-origin NETs, not C7A.094.

Impact

Risk of selecting incorrect primary code for pancreatic NETs.

Mitigation Strategy

Regular training on code differentiation and documentation requirements.

Documentation errors, coding pitfalls, and audit risks are interconnected aspects of medical coding and billing. Addressing all three areas helps ensure accurate coding, optimal reimbursement, and regulatory compliance.

Frequently Asked Questions

Common questions about ICD-10 coding for Pancreatic Neuroendocrine Tumor, with expert answers to help guide accurate code selection and documentation.

Documentation Templates for Pancreatic Neuroendocrine Tumor

Use these documentation templates to ensure complete and accurate documentation for Pancreatic Neuroendocrine Tumor. These templates include all required elements for proper coding and billing.

Pathology Report for Nonfunctional PNET

Specialty: Pathology

Required Elements

  • Tumor size
  • Histological grade
  • Functionality status
  • Immunohistochemistry results

Examples: Poor vs. Good Documentation

Poor Documentation Example
Pancreatic neuroendocrine tumor
Good Documentation Example
4.2 cm well-differentiated pancreatic neuroendocrine tumor (G2, Ki-67 8%) in body of pancreas, nonfunctional, chromogranin A positive, synaptophysin positive.
Explanation
The good example provides specific details necessary for accurate coding and billing.

Need help with ICD-10 coding for Pancreatic Neuroendocrine Tumor? Ask your questions below.

Ask about any ICD-10 CM code, or paste a medical note

We build tools for
clinician happiness.

Learn More at Freed.ai
Back to HomeBeta

Built by Freed

Try Freed for free for 7 days.

Learn more