Hypokalemia associated with a solitary pulmonary nodule A case report

被引:0
作者
Saeian, Samira [1 ]
Ghayumi, Seiyed Mohammad Ali [1 ]
Shams, Mesbah [2 ]
机构
[1] Shiraz Univ Med Sci, Dept Internal Med, Dept Internal Med, Shiraz, Iran
[2] Shiraz Univ Med Sci, Endocrine & Metab Res Ctr, Shiraz, Iran
关键词
ACTH syndrome; ectopic; carcinoid tumor; case report; cushing syndrome; hypokalemia; neuroendocrine tumors; solitary pulmonary nodule; CUSHINGS-SYNDROME; MANAGEMENT; DIAGNOSIS; FEATURES;
D O I
10.1097/MD.0000000000005046
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Differential diagnosis of hypokalemia and adrenocorticotropic hormone (ACTH)-dependent Cushing's syndrome often presents challenging in endocrinology and requires careful clinical, biochemical, radiological, and pathological investigations. Hypokalemia is a common abnormality and systematic approach is required to avoid delays in diagnosis of important underlying causes. Case Summary: A 49-year-old woman presented with moderate hypokalemia. Further evaluation showed hypercortisolism due to ectopic ACTH secretion. Chest computed tomography (CT) revealed a peripheral solitary pulmonary nodule. Excision biopsy of the nodule showed carcinoid tumor. After excision biopsy, all of the patient's symptoms improved and electrolytes and ACTH levels also became normal. Conclusion: Carciniod tumors should be considered as a differential diagnosis in patients presenting with hypokalemia and ectopic ACTH syndrome. Carcinoid tumor often present as solitary pulmonary nodule and excision biopsy can be curative.
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