Differential diagnosis of hyperandrogenism

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Background: Androgen-producing tumors represent an extremely rare group of hormonally active adrenal neoplasms. Their clinical course is characterized by hirsutism, menstrual irregularities, acne, virilization and other manifestations of hyperandrogenism. This condition should be differentially diagnosed with diseases such as polycystic ovary syndrome (PCOS), congenital adrenal hyperplasia (CAH), Itsenko–Cushing syndrome and adrogen-producing ovarian tumors, which are also characterized by androgen excess.

Case report: The presented clinical case is an example of long-term observation of a reproductive-aged woman with a clinical picture of hyperandrogenism and reproductive dysfunction; she received ineffective treatment for CAH and PCOS at different periods of her life. Multisteroid hormone analysis of blood serum by high-performance liquid chromatography with tandem mass spectrometry (HPLC-MS/MS), genetic testing combined with high-precision imaging techniques made it possible to establish the diagnosis of androgen-producing adrenal mass as the underlying cause of the disease more than 20 years after the appearance of the first symptoms. After performing adrenalectomy for the tumor, the level of androgens and their metabolites became normal, and the menstrual cycle restored.

Conclusion: Patients with manifestations of hyperandrogenism should have laboratory evaluation of possible hormonal disorders, imaging of the adrenal glands and ovaries (pelvic MRI, MSCT of the retroperitoneal space), and genetic testing for CYP21A2 gene mutations, when necessary, to exclude the excessive androgen production or adrenocortical tumorigenesis. In order to identify the source of hyperandrogenism, multisteroid blood analysis may be performed as an additional method using HPLC-MS/MS.

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Sobre autores

Ksenia Ivashchenko

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: kseniya223@mail.ru
ORCID ID: 0000-0002-0786-7809

Endocrinologist, PhD Student

Rússia, Moscow

Natalya Molashenko

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: molashenko@mail.ru
ORCID ID: 0000-0001-6265-1210
Código SPIN: 5679-2808

PhD, Endocrinologist

Rússia, Moscow

Nadezhda Platonova

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: doc-platonova@inbox.ru
ORCID ID: 0000-0001-6388-1544
Código SPIN: 4053-3033

Dr. Med. Sci., Professor, Head of the Department of Therapeutic Endocrinology

Rússia, Moscow

Anna Roslyakova

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: aroslyakova12@gmail.com
ORCID ID: 0000-0003-1857-5083
Código SPIN: 5984-4175

Endocrinologist

Rússia, Moscow

Vitaly Ioutsi

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: vitalik_org@mail.ru
ORCID ID: 0000-0001-9002-1662
Código SPIN: 9734-0997

PhD, Head of the Laboratory of Metabolomic and Proteomic Studies

Rússia, Moscow

Maxim Ovcharov

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: ovcharov.maksim@endocrincentr.ru
ORCID ID: 0000-0001-7879-2034
Código SPIN: 6999-1893

PhD, Senior Researcher at the Laboratory of Metabolomic and Proteomic Studies

Rússia, Moscow

Maria Antsupova

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: masha_ancupova@mail.ru

Researcher at the Laboratory of Metabolomic and Proteomic Studies

Rússia, Moscow

Anastasia Lapshina

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: anastasya.lapshina@endocrincentr.ru
ORCID ID: 0000-0003-4353-6705

PhD, Pathologist

Rússia, Moscow

Svetlana Buryakina

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: sburyakina@yandex.ru
ORCID ID: 0000-0001-9065-7791
Código SPIN: 5675-0651

PhD, Radiologist

Rússia, Moscow

Dmitry Beltsevich

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: belts67@gmail.com
ORCID ID: 0000-0001-7098-4584

Dr. Med. Sci., Professor

Rússia, Moscow

Nikolay Kuznetsov

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: kuznetsov-enc@yandex.ru
ORCID ID: 0000-0002-9419-7013
Código SPIN: 8412-1098

Dr. Med. Sci., Professor

Rússia, Moscow

Elena Andreeva

National Medical Research Center for Endocrinology, Ministry of Health of Russia; Russian University of Medicine, Ministry of Health of Russia

Email: endogin@mail.ru
ORCID ID: 0000-0001-8425-0020
Código SPIN: 1239-2937

Dr. Med. Sci., Professor, Director of the Institute of Reproductive Medicine

Rússia, Moscow; Moscow

Ekaterina Troshina

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Email: troshina@inbox.ru
ORCID ID: 0000-0002-8520-8702
Código SPIN: 8821-8990

Dr. Med. Sci., Professor, Corresponding Member of the RAS

Rússia, Moscow

Galina Melnichenko

National Medical Research Center for Endocrinology, Ministry of Health of Russia

Autor responsável pela correspondência
Email: teofrast2000@mail.ru
ORCID ID: 0000-0002-5634-7877
Código SPIN: 8615-0038

Dr. Med. Sci., Professor, Corresponding Member of the RAS, Deputy Director for Scientific Work

Rússia, Moscow

Bibliografia

  1. Tong A., Jiang J., Wang F., Li C., Zhang Y., Wu X. Pure androgen-producing adrenal tumor: clinical features and pathogenesis. Endocr. Pract. 2017; 23(4): 399-407. https://dx.doi.org/10.4158/EP161580.OR.
  2. Conway G., Dewailly D., Diamanti-Kandarakis E., Escobar-Morreale H.F., Franks S., Gambineri A. et al.; ESE PCOS Special Interest Group. The polycystic ovary syndrome: a position statement from the European Society of Endocrinology. Eur. J. Endocrinol. 2014; 171(4): P1-P29. https:// dx.doi.org/10.1530/EJE-14-0253.
  3. Carmina E. Diagnosis of polycystic ovary syndrome: from NIH criteria to ESHRE-ASRM guidelines. Minerva Ginecol. 2004; 56(1): 1-6.
  4. Wong F.C.K., Chan A.Z., Wong W.S., Kwan A.H.W., Law T.S.M., Chung J.P.W. et al. Hyperandrogenism, elevated 17-hydroxyprogesterone and its urinary metabolites in a young woman with ovarian steroid cell tumor, not otherwise specified case report and review of the literature. Case Rep. Endocrinol. 2019; 2019: 9237459. https://dx.doi.org/10.1155/2019/9237459.
  5. Молашенко Н.В., Сазонова А.И., Трошина Е.А. Врожденная дисфункция коры надпочечников у взрослых пациентов: алгоритм диагностики и лечения. Consilium Medicum. 2017; 19(4): 70-4. [Molashenko N.V., Sazonova A.I., Troshina E.A. Congenital adrenal hyperplasia (21-hydroxylase deficiency) in adulthood patients: diagnosis and treatment. Consilium Medicum. 2017; 19(4): 70-4. (in Russian)].
  6. Ebbehoj A., Li D., Kaur R.J., Zhang C., Singh S., Li T. et al. Epidemiology of adrenal tumours in Olmsted County, Minnesota, USA: a population-based cohort study. Lancet Diabetes Endocrinol. 2020; 8(11): 894-902. https:// dx.doi.org/10.1016/S2213-8587(20)30314-4.
  7. Moreno S., Montoya G., Armstrong J., Leteurtre E., Aubert S., Vantyghem M.C. et al. Profile and outcome of pure androgen-secreting adrenal tumors in women: experience of 21 cases. Surgery. 2004; 136(6): 1192-8. https://dx.doi.org/10.1016/j.surg.2004.06.046.
  8. Elhassan Y.S., Idkowiak J., Smith K., Asia M., Gleeson H., Webster R. et al. Causes, patterns, and severity of androgen excess in 1205 consecutively recruited women. J. Clin. Endocrinol. Metab. 2018; 103(3): 1214-23. https:// dx.doi.org/10.1210/jc.2017-02426.
  9. Liao Z., Gao Y., Zhao Y., Wang Z., Wang X., Zhou J. et al. Pure androgen-secreting adrenal tumor (PASAT): a rare case report of bilateral PASATs and a systematic review. Front. Endocrinol. (Lausanne). 2023; 14: 1138114. https://dx.doi.org/10.3389/fendo.2023.1138114.
  10. Cordera F., Grant C., Van Heerden J., Thompson G., Young W. Androgen-secreting adrenal tumors. Surgery. 2003; 134(6): 874-80; discussion 880. https://dx.doi.org/10.1016/S0039-6060(03)00410-0.
  11. Sciarra F., Tosti-Croce C., Toscano V. Androgen-secreting adrenal tumors. Minerva Endocrinol. 1995; 20(1): 63-8.
  12. Kotidis E., Bitsianis S., Galanos-Demiris K., Christidis P., Mantzoros I., Ioannidis O. et al. Case report: a virilizing adrenal oncocytoma. Front. Surg. 2021; 8: 646459. https://dx.doi.org/10.3389/fsurg.2021.646459.
  13. Speiser P.W., Arlt W., Auchus R.J., Baskin L.S., Conway G.S., Merke D.P. et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. J. Clin. Endocrinol. Metab. 2018; 103(11): 4043-8. https://dx.doi.org/10.1210/jc.2018-01865.
  14. Spaulding S.W., Masuda T., Osawa Y. Increased 17 beta-hydroxysteroid dehydrogenase activity in a masculinizing adrenal adenoma in a patient with isolated testosterone overproduction. J. Clin. Endocrinol. Metab. 1980; 50(3): 537-40. https://dx.doi.org/10.1210/jcem-50-3-537.
  15. Tsai W.H., Wong C.H., Dai S.H., Tsai C.H., Zeng Y.H. Adrenal tumor mimicking non-classic congenital adrenal hyperplasia. Front. Endocrinol. (Lausanne). 2020; 11: 526287. https://dx.doi.org/10.3389/fendo.2020.526287.
  16. LaVoie M., Constantinides V., Robin N., Kyriacou A. Florid hyperandrogenism due to a benign adrenocortical adenoma. BMJ Case Rep. 2018; 2018: bcr2018224804. https://dx.doi.org/10.1136/bcr-2018-224804.
  17. Micić D., Zorić S., Popović V., Janković R., Jancić M., Han R. et al. Androgen-producing bilateral large cortical adrenal adenomas associated with polycystic ovaries in a young female. Postgrad. Med. J. 1992; 68(797): 219-22. https://dx.doi.org/10.1136/pgmj.68.797.219.
  18. Mattox J.H., Phelan S. The evaluation of adult females with testosterone producing neoplasms of the adrenal cortex. Surg. Gynecol. Obstet. 1987; 164(2): 98-101.
  19. Nermoen I., Falhammar H. Prevalence and characteristics of adrenal tumors and myelolipomas in congenital adrenal hyperplasia: a systematic review and meta-analysis. Endocr. Pract. 2020; 26(11): 1351-65. https://dx.doi.org/10.4158/EP-2020-0058.
  20. Jaresch S., Kornely E., Kley H.K., Schlaghecke R. Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia. J. Clin. Endocrinol. Metab. 1992; 74(3): 685-9. https://dx.doi.org/10.1210/jcem.74.3.1311000.
  21. Falhammar H., Torpy D.J. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency presenting as adrenal incidentaloma: a systematic review and meta-analysis. Endocr. Pract. 2016; 22(6): 736-52. https://dx.doi.org/10.4158/EP151085.RA.
  22. Иващенко К.В., Комшилова К.А., Молашенко Н.В., Лавренюк А.А., Лапшина А.М., Ким И.В., Иоутси В.А., Анцупова М.А., Уткина М.В., Платонова Н.М., Трошина Е.А., Мокрышева Н.Г. Образование надпочечника, продуцирующее метаболиты стероидогенеза: клинический случай и краткий обзор. Ожирение и метаболизм. 2023; 20(4): 363-70. [Ivashchenko K.V., Komshilova K.A., Molashenko N.V., Lavrenyuk A.A., Lapshina A.M., Kim I.V., Ioutsi V.A., Antsupova M.A., Utkina M.V., Platonova N.M., Troshina E.A., Mokrysheva N.G. Steroid metabolites producing adenoma: a case report. Obesity and Metabolism. 2023; 20(4): 363-70. (in Russian)]. https://dx.doi.org/10.14341/omet13050.
  23. Kamilaris T.C., DeBold C.R., Manolas K.J., Hoursanidis A., Panageas S., Yiannatos J. Testosterone-secreting adrenal adenoma in a peripubertal girl. JAMA. 1987; 258(18): 2558-61.
  24. Witchel S.F., Pinto B., Burghard A.C., Oberfield S.E. Update on adrenarche. Curr. Opin. Pediatr. 2020; 32(4): 574-81. https://dx.doi.org/10.1097/MOP.0000000000000928.

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1. JATS XML
2. Fig. 1. Adrenal MSCT: A. Native phase. B. Arterial phase. В. Venous phase. D. Delayed phase

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3. Fig. 2. Pathomorphological findings of the adrenal gland. Diffuse tumour growth (3.6 cm in size) of the right adrenal gland tissue is determined, mainly of solid structure consisting of large irregularly shaped cells with granular eosinophilic cytoplasm and polymorphic nuclei. There are focal haemorrhages in the thickness of the tumour tissue. No signs of invasion of its own capsule and/or vessels were revealed. Haematoxylin and eosin staining. A - x300. B - x400

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4. Fig. 3. Disorders of synthesis of steroidogenesis enzymes

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