A Rare Case of Metastatic Adrenocorticotrophic Hormone – Secreting Pancreatic Neuroendocrine Tumor Causing Ectopic Cushing Syndrome in a 46-Year-Old Woman

Jessica Y. Huang; Nikitha A. Cherayil; Paul Boyd; Maher Ali; Shazia Samanani

doi:10.12659/AJCR.945653

03 April 2025 : Case report USA

A Rare Case of Metastatic Adrenocorticotrophic Hormone – Secreting Pancreatic Neuroendocrine Tumor Causing Ectopic Cushing Syndrome in a 46-Year-Old Woman

Challenging differential diagnosis, Rare disease

Jessica Y. Huang^1ABCDEF, Nikitha A. Cherayil

^2CDEF, Paul Boyd

^1ACE, Maher Ali^3BCD, Shazia Samanani^1ABCDEF*

DOI: 10.12659/AJCR.945653

Am J Case Rep 2025; 26:e945653

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Figure 3. Axial view from an abdominal MRI with and without contrast, that revealed a 3.0×2.3×2.3 cm mass in the pancreatic head causing obstruction and significant dilation of the main pancreatic duct, which was concerning for malignancy. MRI, magnetic resonance imaging.

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A Rare Case of Metastatic Adrenocorticotrophic Hormone – Secreting Pancreatic Neuroendocrine Tumor Causing Ectopic Cushing Syndrome in a 46-Year-Old Woman

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