Abstract
Despite the rapid development and improvement of diagnostic capabilities in oncology and endocrinology, the diagnosis of neoplastic hypercorticism syndrome remains one of the most complex and unresolved issue of modern medicine. The aim — to find out the possibility of dependence of the level of adrenocorticotropic hormone of the peripheral blood on the localization and spread of neuroendocrine tumors of the chest accompanied by ectopic
Cushing’s syndrome at an early, pre-visual stage of diagnosis. Material and methods. The literature data, which contained information about the change in the level of adrenocorticotropic hormone and the degree of spread of the tumor process of 71 patients with neuroendocrine tumors of the chest, were analyzed. According to the localization of tumors, patients were divided into 3 clinical groups. The first group (bronchopulmonary carcinoid) consisted of 30 patients, including 23 patients with a local tumor process; second group (small cell lung cancer) — 4 patients, all with spread process; the third group (carcinoid/thymus carcinoma) — 37 patients, including 17 patients with local process. The indicator of the level of adrenocorticotropic hormone in the peripheral blood of patients is presented as the ratio: the level of adrenocorticotropic hormone of the patient / value of the upper limit of normal. Results. The highest level of adrenocorticotropic hormone was identified in the group of small cell lung cancer — an increase of 11.2±9.89 times, on the contrary, in the group of thymomas — 7.4±7.7 times (p <0.05), while in the subgroup of the local stage thymomas the level is slightly higher than in the group of spread stage thymomas — an increase of 8.6±8.43 and 6.38±7.08 times, respectively (p<0.05). In the group of bronchopulmonary carcinoid with an average increase in the level of adrenocorticotropic hormone in 3.28±2.54 times in the general group as well as in the subgroup with local tumor process the average level of adrenocorticotropic hormone is higher than in the group with the spread process — an increase of 3.45±2,78 and 2.72±1.53 times, respectively (p<0.05). Conclusion. Based on the results of the data obtained, it became possible to modify the diagnostic algorithm on a case-by-case basis for patients with this
pathology, which made it possible to make an economically and radiologically reasonable choice of a further diagnostic step.
References
Hernández I, Espinosa-de-los-Monteros A, Mendoza V et al. Ectopic ACTH-Secreting Syndrome: A Single Center Experience Report with a High Prevalence of Occult Tumor. Archives of Medical Research. 2006;37(8):976-980. doi:10.1016/j.arcmed.2006.05.015.
Findling J, Raff H. DIAGNOSIS OF ENDOCRINE DISEASE: Differentiation of pathologic/neoplastic hypercortisolism (Cushing’s syndrome) from physiologic/non-neoplastic hypercortisolism (formerly known as pseudo-Cushing’s syndrome). European Journal of Endocrinology. 2017;176(5): R205-R216. doi:10.1530/eje‑16-0946.
Wagner-Bartak N, Baiomy A, Habra M et al. Cushing Syndrome: Diagnostic Workup and Imaging Features, With Clinical and Pathologic Correlation. American Journal of Roentgenology. 2017;209(1):19-32. doi:10.2214/ajr.16.17290.
Findling J, Raff H. DIAGNOSIS OF ENDOCRINE DISEASE: Differentiation of pathologic/neoplastic hypercortisolism (Cushing’s syndrome) from physiologic/non-neoplastic hypercortisolism (formerly known as pseudo-Cushing’s syndrome). European Journal of Endocrinology. 2017;176(5): R205-R216. doi:10.1530/eje‑16-0946.
Barbot M, Trementino L, Zilio M et al. Second-line tests in the differential diagnosis of ACTH-dependent Cushing’s syndrome. Pituitary. 2016;19(5):488-495. doi:10.1007/s11102-016-0729-y.
Hall W. Pituitary Magnetic Resonance Imaging in Normal Human Volunteers: Occult Adenomas in the General Population. Annals of Internal Medicine. 1994;120(10):817. doi:10.7326/0003-4819-120-10-199405150-00001.
Benveniste M, Rosado-de-Christenson M, Sabloff B, Moran C, Swisher S, Marom E. Role of Imaging in the Diagnosis, Staging, and Treatment of Thymoma. RadioGraphics. 2011;31(7):1847- 1861. doi:10.1148/rg.317115505.
Isidori A, Sbardella E, Zatelli M et al. Conventional and Nuclear Medicine Imaging in Ectopic Cushing’s Syndrome: A Systematic Review. The Journal of Clinical Endocrinology & Metabolism. 2015;100(9):3231-3244. doi:10.1210/jc.2015-1589.
Kuznetsov N, Marova E, Latkina N, Lanshchakov K, Dobreva E, Krylov V. Difficulties in the Diagnosis of ACTH-ectopic Tumors. Case Report. Endocrine Surgery. 2014;8(2):9. doi:10.14341/serg201429-13.
Penezic Z, Savic S, Vujovic S, Tatic S, Ercegovac M, Drezgic M. Ectopic corticotroph syndrome. Srpski arhiv za celokupno lekarstvo. 2004;132(1-2):28-32. doi:10.2298/sarh0402028p.
Dobreva E, Krylov V, Marova E, Kuznetsov N, Latkina N. ACTHproducingneuroendocrine tumor of thymus with recurrences. Clinical case. Endocrine Surgery. 2015;9(2):31. doi:10.14341/ serg2015231-34.
Gupta R, Sharma A, Dinda A, Arora R. Primary neuroendocrine carcinoma of thymus: A rare cause of Cushing’s syndrome. Indian Journal of Pathology and Microbiology. 2010;53(1):148. doi:10.4103/0377-4929.59210.
Mandaliya R, Hughes L, Auerbach H, LePar F. Small Cell Lung Cancer Presenting as Severe Thrombocytopenia and Refractory Hypokalemia. Case Reports in Oncological Medicine. 2014;2014:1-4. doi:10.1155/2014/874831.
https://endojournals.ru/index.php/omet/article/view/5246/3064
Menezes Nunes J, Pinho E, Camões I et al. A Challenging Case of an Ectopic Cushing Syndrome. Case Reports in Medicine. 2014;2014:1-8. doi:10.1155/2014/413136.
Dzeranova L, Skuridina D, Voronkova I et al. ACTH overexpressing pituitary hyperplasia in a patient with ectopic ACTH-syndrome due to carcinoid of the lung. Obesity and metabolism. 2015;12(1):52. doi:10.14341/omet2015152-59.
Thomas N, Sudeep K, Korula A, Asha H, Alexander M, Gnanamuthu B. Cushing’s syndrome in a case of thymic carcinoma. Indian Journal of Endocrinology and Metabolism. 2011;15(4):346. doi:10.4103/2230-8210.85601.
Kenchaiah M, Hyer S. Cushing’s Syndrome due to Ectopic ACTH from Bronchial Carcinoid: A Case Report and Review. Case Reports in Endocrinology. 2012;2012:1-4. doi:10.1155/2012/215038.
Salgado L, Fragoso M, Knoepfelmacher M et al. Ectopic ACTH syndrome: our experience with 25 cases. European Journal of Endocrinology. 2006;155(5):725-733. doi:10.1530/eje.1.02278.
Coates P, Doniach I, Howlett T, Rees L, Besser G. Immunocytochemical study of 18 tumours causing ectopic Cushing’s syndrome. Journal of Clinical Pathology. 1986;39(9):955-960. doi:10.1136/jcp.39.9.955.