Association of endogenous hypercortisolism with hepatic hemangiomas in cushing’s disease: a retrospective cohort study - Report - MDSpire

Association of endogenous hypercortisolism with hepatic hemangiomas in cushing’s disease: a retrospective cohort study

  • By

  • Lanlan Zhao

  • Jiao Liu

  • Na Li

  • Ying Wei

  • Pin Wang

  • Jie Li

  • Songyun Zhang

  • June 22, 2026

  • 0 min

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Link Between Endogenous Hypercortisolism and Hepatic Hemangiomas in Cushing's Disease

Overview

This study investigates the prevalence of hepatic hemangiomas (HH) in patients with Cushing's disease (CD) and identifies associated risk factors.

Background

Cushing's disease, caused by ACTH-secreting pituitary tumors, leads to excessive cortisol levels and various complications, including cardiovascular risks. Hepatic hemangiomas are the most common benign liver tumors, often asymptomatic but potentially serious when large. Understanding the relationship between endogenous hypercortisolism and HH is crucial for managing patients with CD.

Data Highlights

This study included 315 patients with ACTH-PitNETs, with 96 diagnosed with Cushing's disease. Among these, 18 patients had hepatic hemangiomas, indicating a significant prevalence in this cohort.

Key Findings

  • The study identified 18 out of 96 patients with Cushing's disease having hepatic hemangiomas.
  • Previous case reports suggest that exogenous glucocorticoids may promote HH progression.
  • Risk factors for HH in CD patients were analyzed using various statistical methods, including logistic regression.
  • The relationship between endogenous cortisol levels and HH has not been systematically investigated prior to this study.

Clinical Implications

The findings highlight the need for clinicians to consider the potential presence of hepatic hemangiomas in patients with Cushing's disease. Early identification and management of HH may be necessary to prevent complications.

Conclusion

This study provides evidence of a significant prevalence of hepatic hemangiomas in patients with Cushing's disease, emphasizing the importance of monitoring for this condition in clinical practice.

Related Resources & Content

  1. The Journal of Clinical Endocrinology & Metabolism, 2023 -- The Development of Fatty Liver Disease in Patients with Cushing Syndrome
  2. The Journal of Clinical Endocrinology & Metabolism, 2023 -- Increased Cancer Risk Linked to Cushing Syndrome: Findings from a Nationwide Cohort Analysis
  3. The Journal of Clinical Endocrinology & Metabolism, 2023 -- Altered Microbiome Signature in Cushing's Syndrome Persists Beyond Remission
  4. Consensus on the diagnosis of Cushing’s disease: a collaborative statement from the Korean Endocrine Society and Japan Endocrine Society, 2026
  5. Journal of Neuro-Oncology (Springer) — Unsupervised clustering analysis reveals distinct postoperative cortisol trajectories following pituitary adenoma resection in Cushing’s disease
  6. Consensus on the diagnosis of Cushing’s disease: a collaborative statement from the Korean Endocrine Society and Japan Endocrine Society - PMC
  7. Efficacy and safety of relacorilant for the treatment of patients with Cushing's syndrome (GRACE): a multicentre, phase 3, double-blind, placebo-controlled, randomised-withdrawal study - PubMed
  8. EASL Clinical Practice Guidelines on the management of benign liver tumours

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