Tumor testicular de remanescente adrenal em homem infértil com hiperplasia adrenal congênita
relato de caso e revisão de literatura
Palavras-chave:
Hiperplasia supra-renal congênita, Tumor de resto supra-renal, Infertilidade, Testículo, MicrocirurgiaResumo
CONTEXTO: Pacientes com hiperplasia adrenal congênita (HAC) por deficiência da 21-hidroxilase podem ter a síntese de cortisol e de aldosterona prejudicada. Homens com HAC têm baixas taxas de fertilidade em comparação com a população normal, e isso está relacionado a tumores testiculares de remanescente adrenal. A associação de azoospermia e tumor testicular sugere uma causa mecânica, principalmente quando o tumor é encontrado no mediastino testicular. O método preferencial de tratamento consiste na corticoterapia intensa. No entanto, quando o tumor não é responsivo à terapia com esteroides, o tratamento cirúrgico deve ser considerado. RELATO DE CASO: Apresentamos o caso de um paciente do sexo masculino com HAC por deficiência da 21-hidroxilase, portador de tumor testicular e azoospermia. Em consulta prévia com endocrinologista, o paciente começou tratamento com baixas doses diárias de corticoide, porém, após 12 meses de tratamento, não houve mudança significativa no espermograma. Embora os níveis de hormônio adrenocortitrófico e 17-hidroxiprogesterona tenham se normalizado, os níveis séricos de hormônio folículoestimulante, hormônio luteinizante e testosterona não se alteraram. Exame ultrassonográfico confirmou testículos bilateralmente diminuídos e heterogêneos, além de área em mosaico na projeção da rede testis bilateralmente. Ressonância nuclear magnética confirmou o achado. Biópsia testicular revelou espermatogênese e espermiogênese preservadas em 20% dos túbulos seminíferos no testículo direito. O paciente foi submetido a cirurgia poupadora testicular, com ressecção tumoral. Após 12 meses de acompanhamento, não houve recorrência tumoral, mas o paciente ainda apresentava azoospermia, sendo integrado no programa de injeção intracitoplasmática de espermatozoides.
Downloads
Referências
Claahsen-van der Grinten HL, Stikkelbroeck NM, Sweep CG, Hermus AR, Otten BJ. Fertility in patients with congenital adrenal hyperplasia. J Pediatr Endocrinol Metab. 2006;19(5):677-85.
Claahsen-van der Grinten HL, Otten BJ, Takahashi S, et al. Testicular adrenal rest tumors in adult males with congenital adrenal hyperplasia: evaluation of pituitary-gonadal function before and after successful testis-sparing surgery in eight patients. J Clin Endocrinol Metab. 2007;92(2):612-5.
Barwick TD, Malhotra A, Webb JA, Savage MO, Reznek RH. Embryology of the adrenal glands and its relevance to diagnostic imaging. Clin Radiol. 2005;60(9):953-9.
Cabrera MS, Vogiatzi MG, New MI. Long term outcome in adult males with classic congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2001;86(7):3070-8.
Stikkelbroeck NM, Otten BJ, Pasic A, et al. High prevalence of testicular adrenal rest tumors, impaired spermatogenesis, and Leydig cell failure in adolescent and adult males with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2001;86(12):5721-8.
Stikkelbroeck NM, Hermus AR, Suliman HM, Jager GJ, Otten BJ. Asymptomatic testicular adrenal rest tumours in adolescent and adult males with congenital adrenal hyperplasia: basal and follow-up investigation after 2.6 years. J Pediatr Endocrinol Metab. 2004;17(4):645-53.
Urban MD, Lee PA, Migeon CJ. Adult height and fertility in men with congenital virilizing adrenal hyperplasia. N Engl J Med. 1978;299(25):1392-6.
Willi U, Atares M, Prader A, Zachmann M. Testicular adrenal-like tissue (TALT) in congenital adrenal hyperplasia: detection by ultrasonography. Pediatr Radiol. 1991;21(4):284-7.
Vanzulli A, DelMaschio A, Paesano P, et al. Testicular masses in association with adrenogenital syndrome: US findings. Radiology. 1992;183(2):425-9.
Avila NA, Premkumar A, Shawker TH, et al. Testicular adrenal rest tissue in congenital adrenal hyperplasia: findings at Gray-scale and color Doppler US. Radiology. 1996;198(1):99-104.
Wilkins L, Fleishmann W, Howard JE. Macrogenitosomia precox associated with hyperplasia of the androgenic tissue of the adrenal and death from corticoadrenal insufficiency case report. Endocrinology. 1940;26(3):385-95. Available from: http://endo.endojournals.org/cgi/content/abstract/26/3/385. Accessed in 2011 (Feb 21).
Rich MA, Keating MA. Leydig cell tumors and tumors associated with congenital adrenal hyperplasia. Urol Clin North Am. 2000;27(3):519-28, x.
Knudsen JL, Savage A, Mobb GE. The testicular‘tumor’of adrenogenital syndrome--a persistent diagnostic pitfall. Histopathology. 1991;19(5):468-70.
Kim I, Young RH, Scully RE. Leydig cell tumors of the testis. A clinicopathological analysis of 40 cases and review of the literature. Am J Surg Pathol. 1985;9(3):177-92.
Witchel SF, Nayak S, Suda-Hartman M, Lee PA. Newborn screening for 21-hydroxylase deficiency: results of CYP21 molecular genetic analysis. J Pediatr. 1997;131(2):328-31.
Allen DB, Hoffman GL, Fitzpatrick P, et al. Improved precision of newborn screening for congenital adrenal hyperplasia using weight-adjusted criteria for 17-hydroxyprogesterone levels. J Pediatr. 1997;130(1):128-33.
Gruñeiro-Papendieck L, Prieto L, Chiesa A, et al. Neonatal screening program for congenital adrenal hyperplasia: adjustments to the recall protocol. Horm Res. 2001;55(6):271-7.
Merke DP, Bornstein SR. Congenital adrenal hyperplasia. Lancet. 2005;365(9477):2125-36.
Joint LWPES/ESPE CAH Working Group. Consensus statement on 21- hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. J Clin Endocrinol Metab. 2002;87(9):4048-53.
Speiser PW. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Endocrinol Metab Clin North Am. 2001;30(1):31-59, vi.
Mesino S, Jaffe RB. Developmental and functional biology of the primate fetal adrenal cortex. Endocr Rev. 1997;18(3):378-403.
Fujieda K, Tajima T. Molecular basis of adrenal insufficiency. Pediatr Res. 2005;57(5 Pt 2):62R-69R.
Graham LS. Celiac accessory adrenal glands. Cancer. 1953;6:149-52. Available from: http://onlinelibrary.wiley.com/doi/10.1002/1097-0142(195301)6:1%3C149::AID-CNCR2820060115%3E3.0.CO;2-8/pdf. Accessed in 2011 (Feb 21).
Falls JL. Accessory adrenal cortex in the broad ligament: incidence and functional significance. Cancer. 1955;8(1):143-50.
Dahl EV, Bahn RC. Aberrant adrenal contical tissue near the testis in human infants. Am J Pathol. 1962;40:587-98.
Symonds DA, Driscoll SG. An adrenal cortical rest within the fetal ovary: report of a case. Am J Clin Pathol. 1973;60(4):562-4.
Rutgers JL, Young RH, Scully RE. The testicular “tumor” of the adrenogenital syndrome. A report of six cases and review of the literature on testicular masses in patients with adrenocortical disorders. Am J Surg Pathol. 1988;12(7):503-13.
Cutfield RG, Bateman JM, Odell WD. Infertility caused by bilateral testicular masses secondary to congenital adrenal hyperplasia (21- hydroxylase deficiency). Fertil Steril. 1983;40(6):809-14.
Cunnah D, Perry L, Dacie JA, et al. Bilateral testicular tumours in congenital adrenal hyperplasia: a continuing diagnostic and therapeutic dilemma. Clin Endocrinol (Oxf ). 1989;30(2):141-7.
Blumberg-Tick J, Boudou P, Nahoul K, Schaison G. Testicular tumors in congenital adrenal hyperplasia: steroid measurements from adrenal and spermatic veins. J Clin Endocrinol Metab. 1991;73(5):1129-33.
Combes-Moukhovsky ME, Kottler ML, Valensi P, et al. Gonadal and adrenal catheterization during adrenal suppression and gonadal stimulation in a patient with bilateral testicular tumors and congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1994;79(5):1390-4.
Srikanth MS, West BR, Ishitani M, et al. Benign testicular tumors in children with congenital adrenal hyperplasia. J Pediatr Surg. 1992;27(5):639-41.
Clark RV, Albertson BD, Munabi A, et al. Steroidogenic enzyme activities, morphology, and receptor studies of a testicular adrenal rest in a patient with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1990;70(5):1408-13.
Moore GW, Lacroix A, Rabin D, McKenna TJ. Gonadal dysfunction in adult men with congenital adrenal hyperplasia. Acta Endocrinol (Copenh). 1980;95(2):185-93.
Radfar N, Bartter FC, Easley R, et al. Evidence for endogenous LH suppression in a man with bilateral testicular tumors and congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1977;45(6):1194-204.
Avila NA, Shawker TS, Jones JV, Cutler GB Jr, Merke DP. Testicular adrenal rest tissue in congenital adrenal hyperplasia: serial sonographic and clinical findings. AJR Am J Roentgenol. 1999;172(5):1235-8.
Peggy P, Francois D, Francois T, et al. Adrenal rest tissue in gonads in 70 French patients with classical congenital adrenal hyperplasia (21 hydroxylase deficiency). European Congress of Endocrinology; 2007. Budapest, Hungary, 28 April – 02 May 2007. Endocrine Abstracts. 2007;14:P632. Available from: http://www.endocrine-abstracts.org/ea/0014/ea0014p632.htm. Accessed in 2011 (Feb 21).
Jensen TK, Andersson AM, Hjollund NH, et al. Inhibin B as a serum marker of spermatogenesis: correlation to differences in sperm concentration and follicle-stimulating hormone levels. A study of 349 Danish men. J Clin Endocrinol Metab. 1997;82(12):4059-63.
Anawalt BD, Bebb RA, Matsumoto AM, et al. Serum inhibin B levels reflect Sertoli cell function in normal men and men with testicular dysfunction. J Clin Endocrinol Metab. 1996;81(9):3341-5.
Andersson AM, Petersen JH, Jørgensen N, Jensen TK, Skakkebaek NE. Serum inhibin B and follicle-stimulating hormone levels as tools in the evaluation of infertile men: significance of adequate reference values from proven fertile men. J Clin Endocrinol Metab. 2004;89(6):2873-9.
Lee MM, Donahoe PK, Silverman BL, et al. Measurements of serum müllerian inhibiting substance in the evaluation of children with nonpalpable gonads. N Engl J Med. 1997;336(21):1480-6.
Martinez-Aguayo A, Rocha A, Rojas N, et al. Testicular adrenal rest tumors and Leydig and Sertoli cell function in boys with classical congenital adrenal hyperplasia. J Clin Endocrin Metab. 2007;92(12):4583-9.
Claahsen-van der Grinten HL, Otten BJ, Sweep FC, et al. Testicular tumors in patients with congenital adrenal hyperplasia due to 21- hydroxylase deficiency show functional features of adrenocortical tissue. J Clin Endocrinol Metab. 2007;92(9):3674-80.
Stikkelbroeck NM, Hoefsloot LH, de Wijs IJ, et al. CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations. J Clin Endocrinol Metab. 2003;88(8):3852-9.
Walker BR, Skoog SJ, Winslow BH, Canning DA, Tank ES. Testis sparing surgery for steroid unresponsive testicular tumors of the adrenogenital syndrome. J Urol. 1997;157(4):1460-3.
Bonaccorsi AC, Adler I, Figueiredo JG. Male infertility due to congenital adrenal hyperplasia: testicular biopsy findings, hormonal evaluation, and therapeutic results in three patients. Fertil Steril. 1987;47(4):664-70.
Augarten A, Weissenberg R, Pariente C, Sack J. Reversible male infertility in late onset congenital adrenal hyperplasia. J Endocrinol Invest. 1991;14(3):237-40.
New MI, Wilson RC. Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess. Proc Natl Acad Sci U S A. 1999;96(22):12790-7.
Murphy H, George C, de Kretser D, Judd S. Successful treatment with ICSI of infertility caused by azoospermia associated with adrenal rests in the testes: case report. Hum Reprod. 2001;16(2):263-7.
Sugino Y, Usui T, Okubo K, et al. Genotyping of congenital adrenal hyperplasia due to 21-hydroxylase deficiency presenting as male infertility: case report and literature review. J Assist Reprod Genet. 2006;23(9-10):377-80.
Kalachanis I, Rousso D, Kourtis A, et al. Reversible infertility, pharmaceutical and spontaneous, in a male with late onset congenital adrenal hyperplasia, due to 21-hydroxylase deficiency. Arch Androl. 2002;48(1):37-41.
Iwamoto T, Yajima M, Tanaka H, Minagawa N, Osada T. [A case report: reversible male infertility due to congenital adrenal hyperplasia]. Nippon Hinyokika Gakkai Zasshi. 1993;84(11):2031-4.
Yang RM, Fefferman RA, Shapiro CE. Reversible infertility in a man with 21-hydroxylase deficiency congenital adrenal hyperplasia. Fertil Steril. 2005;83(1):223-5.
Fernandes VO, Barros AI, Quidute AR, et al. Tumores testiculares bilaterais por hiperplasia congênita de restos adrenais [Bilateral testicular tumors caused by congenital adrenal rest hyperplasia]. Arq Bras Endocrinol Metabol. 2009;53(8):1052-8.
Downloads
Publicado
Como Citar
Edição
Seção
Licença

Este trabalho está licenciado sob uma licença Creative Commons Attribution 4.0 International License.