[1] |
|
[2] |
FALHAMMAR H, TORPY D J. Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency presenting as adrenal incidentaloma:a systematic review and meta-analysis[J]. Endocr Pract, 2016, 22(6):736-752. DOI: 10.4158/EP151085.RA.
|
[3] |
|
[4] |
|
[5] |
|
[6] |
|
[7] |
|
[8] |
|
[9] |
|
[10] |
|
[11] |
NERMOEN I, RØRVIK J, HOLMEDAL S H,et al. High frequency of adrenal myelolipomas and testicular adrenal rest tumours in adult Norwegian patients with classical congenital adrenal hyperplasia because of 21-hydroxylase deficiency[J]. Clin Endocrinol (Oxf), 2011, 75(6):753-759. DOI: 10.1111/j.1365-2265.2011.04151.x.
|
[12] |
GERMAN-MENA E, ZIBARI G B, LEVINE S N. Adrenal myelolipomas in patients with congenital adrenal hyperplasia:review of the literature and a case report[J]. Endocr Pract, 2011, 17(3):441-447. DOI: 10.4158/EP10340.RA.
|
[13] |
JARESCH S, KORNELY E, KLEY H K,et al. Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia[J]. J Clin Endocrinol Metab, 1992, 74(3):685-689. DOI: 10.1210/jcem.74.3.1311000.
|
[14] |
BHATIA V, SHUKLA R, MISHRA S K,et al. Adrenal tumor complicating untreated 21-hydroxylase deficiency in a 5 1/2-year-old boy[J]. Am J Dis Child, 1993, 147(12):1321-1323. DOI: 10.1001/archpedi.1993.02160360063020.
|
[15] |
NERMOEN I, FALHAMMAR H. Prevalence and characteristics of adrenal tumors and myelolipomas in congenital adrenal hyperplasia:a systematic review and meta-analysis[J]. Endocr Pract, 2020, 26(11):1351-1365. DOI: 10.4158/EP-2020-0058.
|
[16] |
VARMA T, PANCHANI R, GOYAL A,et al. A case of androgen-secreting adrenal carcinoma with non-classical congenital adrenal hyperplasia[J]. Indian J Endocrinol Metab, 2013, 17(Suppl 1):S243-245. DOI: 10.4103/2230-8210.119585.
|
[17] |
LIBÉ R, ARLT W, LOUISET E,et al. A feminizing adrenocortical carcinoma in the context of a late onset 21-hydroxylase deficiency[J]. J Clin Endocrinol Metab, 2014, 99(6):1943-1944. DOI: 10.1210/jc.2014-1342.
|
[18] |
LEBEK-SZATANSKA A, NOWAK K M, SAMSEL R,et al. Adrenocortical carcinoma associated with giant bilateral myelolipomas in classic congenital adrenal hyperplasia[J]. Pol Arch Intern Med, 2019, 129(7/8):549-550. DOI: 10.20452/pamw.14788.
|
[19] |
PAKALNISKIS M G, ISHIGAMI K, PAKALNISKIS B L,et al. Adrenal collision tumour comprised of adrenocortical carcinoma and myelolipoma in a patient with congenital adrenal hyperplasia[J]. J Med Imaging Radiat Oncol, 2020, 64(1):67-68. DOI: 10.1111/1754-9485.12961.
|
[20] |
FALKE T H, VAN SETERS A P, SCHABERG A,et al. Computed tomography in untreated adults with virilizing congenital adrenal cortical hyperplasia[J]. Clin Radiol, 1986, 37(2):155-160. DOI: 10.1016/s0009-9260(86)80389-0.
|
[21] |
FASSNACHT M, ARLT W, BANCOS I,et al. Management of adrenal incidentalomas:European Society of Endocrinology clinical practice guideline in collaboration with the European network for the study of adrenal tumors[J]. Eur J Endocrinol, 2016, 175(2):G1-34. DOI: 10.1530/EJE-16-0467.
|
[22] |
|