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DOI 10.26442/00403660.2021.10.201102

Медицинская библиотека · Terapevticheskii arkhiv · 2021

[Clinical and laboratory characteristics and results of treatment of patients with ACTH-producing neuroendocrine tumors of various localization].

Golounina O O, Belaya Z E, Rozhinskaya L Y, Marova E I, Pikunov M Y, Khandaeva P M, Arapova S D, Dzeranova L K, Kuznetsov N S, Fadeev V V, Melnichenko G A, Dedov I I

Аннотация на английскомСтатьяПеревод в очереди

Аннотация

AIM: To study the clinical, biochemical characteristics, treatment results and follow-up of patients with ectopic ACTH syndrome EAS (ACTH adrenocorticotropic hormone ).

MATERIALS AND

METHODS

A retrospective, observational, single-center study of 130 patients with EAS. Demographic information of patients, medical history, results of laboratory and instrumental investigations at the pre- and postoperative stages and follow-up of EAS were analyzed.

RESULTS

The mean age at the diagnosis ranged from 12 to 74 years (Me 40 years [28; 54]). The duration of the disease from the onset of symptoms to the verification of the diagnosis varied from 2 to 168 months (Me 17.5 months [7; 46]). Eighty-one (62,3%) patients had bronchopulmonary NET, 9 thymic carcinoid, 7 pancreatic NET, 5 pheochromocytoma, 1 cecum NET, 1 appendix carcinoid tumor, 1 medullary thyroid cancer and 25 (19.2%) had an occult source of ACTH. The median follow-up period of patients was 27 months [9.75; 61.0] with a maximum follow-up of 372 months. Currently, primary tumor was removed in 82 (63.1%) patients, bilateral adrenalectomy was performed in 23 (18%) patients, in 16 of them there was an occult source of ACTH-producing NET and in 7 patients in order to control hypercortisolism after non-successful surgical treatment. Regional and distant metastases were revealed in 25 (19.2%) patients. At the time of the last observation 59 (72%) patients were exhibited a full recovery, 12 (14.6%) had relapse of the disease and 26 (20%) died from multiple organ failure (n=18), pulmonary embolism (n=4), surgical complications (n=2), disseminated intravascular coagulation syndrome (n=1) or COVID-19 (n=1).

CONCLUSION

In our cohort of patients bronchopulmonary NET are the most frequent cause of EAS (62.3%). Surgical treatment leads to remission of hypercortisolism in 72% cases; the proportion of relapse (14.6%) and fatal outcome (20%) remains frequent in EAS.

Для цитирования: Golounina O O, Belaya Z E, Rozhinskaya L Y, Marova E I, Pikunov M Y, Khandaeva P M, Arapova S D, Dzeranova L K, Kuznetsov N S, Fadeev V V, Melnichenko G A, Dedov I I. [Clinical and laboratory characteristics and results of treatment of patients with ACTH-producing neuroendocrine tumors of various localization].. Terapevticheskii arkhiv. 2021. DOI: 10.26442/00403660.2021.10.201102.

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