What is the ICD-10 (International Classification of Diseases, 10th Revision) code for a Primary Care Physician (PCP) referral to endocrinology due to a history of parathyroid adenoma?

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ICD-10 Code for PCP Referral to Endocrinology for Parathyroid Adenoma History

The appropriate ICD-10 code for a PCP referral to endocrinology due to a history of parathyroid adenoma is D35.1 (Benign neoplasm of parathyroid gland).

Coding Rationale and Clinical Context

  • Parathyroid adenomas are the most common cause of primary hyperparathyroidism (PHPT), accounting for 80-85% of PHPT cases 1, 2
  • When coding for a referral to endocrinology for a patient with history of parathyroid adenoma, the underlying condition (the adenoma itself) should be coded, not just the referral reason 1

Clinical Significance of Parathyroid Adenomas

  • Parathyroid adenomas cause autonomous overproduction of parathyroid hormone (PTH), typically resulting in hypercalcemia 1
  • PHPT is more common in women, with an incidence of 66 per 100,000 person-years versus 25 per 100,000 person-years in men 1
  • Most cases are sporadic, although hereditary causes exist, including multiple endocrine neoplasia (MEN) types 1 and 2A, as well as familial hyperparathyroidism 1

Indications for Specialist Referral

Referral to endocrinology is particularly important in patients with:

  • Parathyroid adenoma diagnosed at age <30 1
  • Parathyroid adenoma with multiple glands involved 1
  • Parathyroid adenoma and thymic or bronchial carcinoid, pancreatic neuroendocrine tumor, pituitary tumor, or adrenal tumor in the same person 1
  • Parathyroid adenoma and a family history of hyperparathyroidism, pituitary adenoma, pancreatic islet cell tumor, or foregut carcinoid tumor 1

Genetic Considerations

  • Patients with parathyroid adenomas meeting certain criteria should be considered for genetic counseling for potential MEN1 (OMIM 131100) or MEN2 (OMIM 171400,155240,162300) syndromes 1
  • Genetic testing is particularly important when parathyroid adenomas occur at a young age or in the context of other endocrine tumors 1

Clinical Course and Management

  • Treatment of PHPT is typically surgical excision of the abnormally functioning parathyroid tissue 1
  • Surgery is indicated even when asymptomatic, given potential negative effects of long-term hypercalcemia 1
  • Two accepted curative operative strategies exist: bilateral neck exploration (BNE) and minimally invasive parathyroidectomy (MIP) 1
  • Persistent or recurrent PHPT may occur, requiring additional imaging and potential reoperation 1

Coding Pitfalls to Avoid

  • Do not use symptom codes (such as hypercalcemia) when the underlying condition (parathyroid adenoma) is known 1
  • Avoid using general endocrine disorder codes when a specific code for the parathyroid neoplasm exists 1
  • If the patient has a genetic syndrome associated with parathyroid adenoma (such as MEN1 or MEN2), consider additional coding to reflect this underlying condition 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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