Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Carcinoid tumor with ectopic Cushing syndrome
- Radiologic Findings
- Abdomen CT shows diffuse thickening of adrenal glands suggesting adrenal hyperplasia. A well-defined nodule with strong enhancement (HU=160) was noted in the left lower lobe. An endocrine evaluation showed a corticotropin-dependent hypercortisolism, which was not suppressed with the administration of high-dose dexamethasone and could not be stimulated with the administration of corticotropin-releasing hormone, a finding that suggested a diagnosis of Cushing's syndrome resulting from the ectopic secretion of corticotropin. There was no evidence of pituitary adenoma on brain MR and inferior petrosal sinus sampling was negative. The nodule in the left lower lobe assumed to be an ACTH producing carcinoid tumor and was resected. Final pathology was an atypical carcinoid tumor.
- Brief Review
- Many bronchopulmonary (BP)-carcinoids are detected incidentally on chest radiographs. Plain radiographs are nonspecific, although BP-carcinoids often appear as an isolated, well-defined hilar or perihilar mass. Once a suspicious lesion is detected on chest radiograph, CT of the chest and upper abdomen should be undertaken to determine the size, characteristics, extent of the primary tumor, involvement of mediastinal lymph nodes, and presence of distant metastases. Typical carcinoid tumor shows a well-defined, spherical or ovoid mass that narrow, deform, and/or obstruct airways. They tend to be vascular and are located close to central bronchi, often near the bifurcation area, whereas atypical carcinoid tumors usually are located peripherally in the lung. Calcification is evident in up to 30% of tumors and manifests in a punctuate or diffuse pattern. Typical as well as atypical carcinoid tumors may be associated with hilar or malignant lymphadenopathy. Cushing syndrome (ectopic production and secretion of ACTH) may occur in ~2% of BP-carcinoids, whereas <1% of individuals with Cushing syndrome have a BP carcinoid. Other, rare endocrine conditions associated with carcinoids include acromegaly, hypercalcemia, and hypoglycemia.
- References
- 1. Limper AH,Carpenter PC,Scheithauer B, et al. The Cushing syndrome induced by bronchial carcinoid tumors. Ann Intern Med. 1992; 117: 209-214
2.Chong S, Lee KS, Chung MJ, Han J, Kwon OJ, Kim TS. Neuroendocrine tumors of the lung: clinical, pathologic, and imaging findings. Radiographics. 2006; 26:41-57
- Keywords
- Lung, Benign tumor,