Literature DB >> 17222630

Clinical and pathological features associated with the testicular tumor of the adrenogenital syndrome.

Richard A Ashley1, Shawn M McGee, Philip A Isotaolo, Stephen A Kramer, John C Cheville.   

Abstract

PURPOSE: Testicular tumor of the adrenogenital syndrome is a rare clinical entity found in young men with endocrine disorders. Histologically it resembles Leydig cell tumor. We 1) reviewed the clinical features of testicular tumor of the adrenogenital syndrome and 2) determined if special histopathological features of the tumor and synaptophysin reactivity could distinguish testicular tumor of the adrenogenital syndrome from Leydig cell tumor.
MATERIALS AND METHODS: We reviewed the medical and pathological records for all patients with testicular tumor of the adrenogenital syndrome seen at our institution from 1978 to 2004. These tumors were examined by histological and immunophenotypic methods for comparison to Leydig cell tumor.
RESULTS: A total of 14 males with an endocrine disorder had pathological evidence of testicular tumor of the adrenogenital syndrome. These tumors were often bilateral (93% or 13 of 14 cases), associated with pain (92% or 12 of 13) and refractory to medical management with high dose exogenous steroids (93% or 13 of 14). Testicular tumor of the adrenogenital syndrome was managed by tumor enucleation in 7 patients (54%) and by radical orchiectomy in 6 (46%). All patients had resolution of pain at 3-month followup. Upon histological review features found to be more common to testicular tumor of the adrenogenital syndrome compared with Leydig cell tumor were nuclear pleiomorphism, low mitotic activity, extensive fibrosis, lymphoid aggregates, adipose metaplasia and prominent lipochrome pigment. Synaptophysin (ICN, Costa Mesa, California) reactivity was strong in testicular tumor of the adrenogenital syndrome but rarely observed in Leydig cell tumor.
CONCLUSIONS: In our series medical treatment failed in patients with testicular tumor of the adrenogenital syndrome and conservative surgical therapy was possible in select individuals. We identified special histopathological and immunophenotypic features, including synaptophysin staining, which distinguish testicular tumor of the adrenogenital syndrome from Leydig cell tumor.

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Year:  2007        PMID: 17222630     DOI: 10.1016/j.juro.2006.09.041

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  13 in total

Review 1.  Adrenal steroidogenesis and congenital adrenal hyperplasia.

Authors:  Adina F Turcu; Richard J Auchus
Journal:  Endocrinol Metab Clin North Am       Date:  2015-06       Impact factor: 4.741

2.  Leydig cell tumor in two brothers with congenital adrenal hyperplasia due to 11-β hydroxylase deficiency: a case report.

Authors:  Pegah Entezari; Abdol Mohammad Kajbafzadeh; Fatemeh Mahjoub; Mohammad Vasei
Journal:  Int Urol Nephrol       Date:  2011-01-23       Impact factor: 2.370

3.  Congenital adrenal hyperplasia presented with bilateral testicular tumor: A case report.

Authors:  Abazar Akbarzadeh Pasha; Hamid Shafi; Mohamad Teimorian; Ghasem Rostami; Khatereh Nasirimehr; Emadoddin Moudi
Journal:  Caspian J Intern Med       Date:  2021

Review 4.  [New 2022 WHO classification of testicular tumours].

Authors:  Alexander Fichtner; Philipp Ströbel; Felix Bremmer
Journal:  Pathologie (Heidelb)       Date:  2022-09-21

5.  Immunophenotypic differences between neoplastic and non-neoplastic androgen-producing cells containing and lacking Reinke crystals.

Authors:  Hector Mesa; Scott Gilles; Milton W Datta; Paari Murugan; Wendy Larson; Susan Dachel; Carlos Manivel
Journal:  Virchows Arch       Date:  2016-10-01       Impact factor: 4.064

6.  Testicular adrenal rest tumors in a patient with congenital adrenal hyperplasia.

Authors:  Jeffrey Dee Olpin; Benjamin Witt
Journal:  J Radiol Case Rep       Date:  2014-02-01

Review 7.  Bilateral testicular masses and adrenal insufficiency: is congenital adrenal hyperplasia the only possible diagnosis? First two cases of TARTS described in Addison-only X-linked adrenoleukodystrophy and a brief review of literature.

Authors:  A S Tresoldi; N Betella; V Hasenmajer; C Pozza; W Vena; B Fiamengo; L Negri; M Cappa; A G A Lania; A Lenzi; A M Isidori; A Pizzocaro
Journal:  J Endocrinol Invest       Date:  2020-07-20       Impact factor: 4.256

8.  BILATERAL ADRENAL AND TESTICULAR MASS IN A PATIENT WITH CONGENITAL ADRENAL HYPERPLASIA.

Authors:  H Piskinpasa; S Ciftci Dogansen; F Kusku Cabuk; D Guzey; N A Sahbaz; Y S Akdeniz; M Mert
Journal:  Acta Endocrinol (Buchar)       Date:  2019 Jan-Mar       Impact factor: 0.877

9.  Testicular adrenal rest "tumor" or Leydig cell tumor? A report of a challenging case with literature review.

Authors:  Hiba Hassan Ali; Alaa Samkari; Haitham Arabi
Journal:  Avicenna J Med       Date:  2013-01

10.  Metachronous Bilateral Testicular Leydig-Like Tumors Leading to the Diagnosis of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome).

Authors:  Josip Vukina; David D Chism; Julie L Sharpless; Mathew C Raynor; Matthew I Milowsky; William K Funkhouser
Journal:  Case Rep Pathol       Date:  2015-08-16
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