Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review

CONTEXT: Synthesis of cortisol and aldosterone is impaired in patients with congenital adrenal hyperplasia (CAH) because of 21-hydroxylase deficiency. Men with CAH have low fertility rates compared with the normal population, and this is related to testicular adrenal rest tumors. Findings of azoospermia in combination with a testicular tumor on ultrasound are likely to have a mechanical cause, especially when in the testicular mediastinum. The preferred treatment method consists of intensive corticoid therapy. However, when the tumor is unresponsive to steroid therapy, surgical treatment should be considered. CASE REPORT: We present the case of a male patient with CAH due to 21-hydroxylase deficiency who presented a testicular tumor and azoospermia. Treatment with low daily corticoid doses had previously been started by an endocrinologist, but after 12 months, no significant change in sperm count was found. Although the adrenocorticotrophic hormone and 17-hydroxyprogesterone levels returned to normal values, the follicle-stimulating hormone (FSH), luteinizing hormone and testosterone levels remained unchanged. Ultrasound examination confirmed that the testicles were small and heterogenous bilaterally, and revealed a mosaic area at the projection of the testis network bilaterally. Magnetic resonance imaging confirmed the finding. Testicular biopsy revealed the presence of preserved spermatogenesis and spermiogenesis in 20% of the seminiferous tubules in the right testicle. The patient underwent testis-sparing tumor resection. After 12 months of follow-up, there was no tumor recurrence but the patient still presented azoospermia and joined an intracytoplasmic sperm injection program.

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Main Authors: Marchini,Giovanni Scala, Cocuzza,Marcello, Pagani,Rodrigo, Torricelli,Fábio César, Hallak,Jorge, Srougi,Miguel
Format: Digital revista
Language:English
Published: Associação Paulista de Medicina - APM 2011
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802011000500010
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spelling oai:scielo:S1516-318020110005000102011-11-07Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature reviewMarchini,Giovanni ScalaCocuzza,MarcelloPagani,RodrigoTorricelli,Fábio CésarHallak,JorgeSrougi,Miguel Adrenal hyperplasia, congenital Adrenal rest tumor Infertility Testis Microsurgery CONTEXT: Synthesis of cortisol and aldosterone is impaired in patients with congenital adrenal hyperplasia (CAH) because of 21-hydroxylase deficiency. Men with CAH have low fertility rates compared with the normal population, and this is related to testicular adrenal rest tumors. Findings of azoospermia in combination with a testicular tumor on ultrasound are likely to have a mechanical cause, especially when in the testicular mediastinum. The preferred treatment method consists of intensive corticoid therapy. However, when the tumor is unresponsive to steroid therapy, surgical treatment should be considered. CASE REPORT: We present the case of a male patient with CAH due to 21-hydroxylase deficiency who presented a testicular tumor and azoospermia. Treatment with low daily corticoid doses had previously been started by an endocrinologist, but after 12 months, no significant change in sperm count was found. Although the adrenocorticotrophic hormone and 17-hydroxyprogesterone levels returned to normal values, the follicle-stimulating hormone (FSH), luteinizing hormone and testosterone levels remained unchanged. Ultrasound examination confirmed that the testicles were small and heterogenous bilaterally, and revealed a mosaic area at the projection of the testis network bilaterally. Magnetic resonance imaging confirmed the finding. Testicular biopsy revealed the presence of preserved spermatogenesis and spermiogenesis in 20% of the seminiferous tubules in the right testicle. The patient underwent testis-sparing tumor resection. After 12 months of follow-up, there was no tumor recurrence but the patient still presented azoospermia and joined an intracytoplasmic sperm injection program.info:eu-repo/semantics/openAccessAssociação Paulista de Medicina - APMSao Paulo Medical Journal v.129 n.5 20112011-01-01info:eu-repo/semantics/reporttext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802011000500010en10.1590/S1516-31802011000500010
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countrycode BR
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libraryname SciELO
language English
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author Marchini,Giovanni Scala
Cocuzza,Marcello
Pagani,Rodrigo
Torricelli,Fábio César
Hallak,Jorge
Srougi,Miguel
spellingShingle Marchini,Giovanni Scala
Cocuzza,Marcello
Pagani,Rodrigo
Torricelli,Fábio César
Hallak,Jorge
Srougi,Miguel
Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review
author_facet Marchini,Giovanni Scala
Cocuzza,Marcello
Pagani,Rodrigo
Torricelli,Fábio César
Hallak,Jorge
Srougi,Miguel
author_sort Marchini,Giovanni Scala
title Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review
title_short Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review
title_full Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review
title_fullStr Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review
title_full_unstemmed Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review
title_sort testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review
description CONTEXT: Synthesis of cortisol and aldosterone is impaired in patients with congenital adrenal hyperplasia (CAH) because of 21-hydroxylase deficiency. Men with CAH have low fertility rates compared with the normal population, and this is related to testicular adrenal rest tumors. Findings of azoospermia in combination with a testicular tumor on ultrasound are likely to have a mechanical cause, especially when in the testicular mediastinum. The preferred treatment method consists of intensive corticoid therapy. However, when the tumor is unresponsive to steroid therapy, surgical treatment should be considered. CASE REPORT: We present the case of a male patient with CAH due to 21-hydroxylase deficiency who presented a testicular tumor and azoospermia. Treatment with low daily corticoid doses had previously been started by an endocrinologist, but after 12 months, no significant change in sperm count was found. Although the adrenocorticotrophic hormone and 17-hydroxyprogesterone levels returned to normal values, the follicle-stimulating hormone (FSH), luteinizing hormone and testosterone levels remained unchanged. Ultrasound examination confirmed that the testicles were small and heterogenous bilaterally, and revealed a mosaic area at the projection of the testis network bilaterally. Magnetic resonance imaging confirmed the finding. Testicular biopsy revealed the presence of preserved spermatogenesis and spermiogenesis in 20% of the seminiferous tubules in the right testicle. The patient underwent testis-sparing tumor resection. After 12 months of follow-up, there was no tumor recurrence but the patient still presented azoospermia and joined an intracytoplasmic sperm injection program.
publisher Associação Paulista de Medicina - APM
publishDate 2011
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802011000500010
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