Acromegaly associated with GIST, non-small cell lung cancer, clear cell renal cancer, myeloma multiplex, medulla oblongata tumor, adrenal adenoma and follicular thyroid nodules

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Published on Wednesday, 13 February 2019

Abstract

BACKGROUND: Acromegaly is associated with increased growth hormone (GH) and insulin-like growth factor-I (IGF-I) secretion which may support tumor development and growth.

CASE PRESENTATION: A 68-year old woman was diagnosed with acromegaly due to typical clinical and hormonal characteristics. While a contrast-enhanced MRI at diagnosis did not reveal a pituitary adenoma, a 5 mm lesion was identified on repeat scanning 13 months later. Abdominal and chest CT showed tumors of the stomach, right adrenal gland and right lung. The CT also showed a hypodense lesion in the liver and heterogeneous echostructure of thyroid gland with left lobe solid-cystic tumor. Somatostatin receptor scintigraphy revealed increased tracer accumulation in the right thyroid lobe. No tracer accumulation was noted at the location of the other tumors. The resected stomach, adrenal, chest and thyroid lesions did not show GH secretion. Patient refused pituitary surgery, and her acromegaly is currently well-controlled with somatostatin analogue therapy. A CT scan 19 months later revealed a contrast enhancing left kidney tumor which was a G1-grade clear cell carcinoma. Four years after the acromegaly diagnosis multiple myeloma was diagnosed with secondary renal amyloidosis. Genetic screening for a paraganglioma gene panel, AIP, MEN1 and CDKN1B mutations were negative. Next-generation cancer panel containing 94 cancer genes did not identify possible unifying gene abnormality in her germline DNA.

CONCLUSIONS: Coexistence of acromegaly and numerous other tumors suggests a common etiology of these disorders. However, no genetic abnormality could be identified with the tests that have been performed.

 

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