Literature DB >> 30882882

Testicular Adrenal Rest Tumors: Current Insights on Prevalence, Characteristics, Origin, and Treatment.

Manon Engels1,2, Paul N Span3, Antonius E van Herwaarden2, Fred C G J Sweep2, Nike M M L Stikkelbroeck4, Hedi L Claahsen-van der Grinten1.   

Abstract

This review provides the reader with current insights on testicular adrenal rest tumors (TARTs), a complication in male patients with congenital adrenal hyperplasia (CAH). In recent studies, an overall TART prevalence of 40% (range, 14% to 89%) in classic patients with CAH is found. Reported differences are mainly caused by the method of detection and the selected patient population. Biochemically, histologically, and molecularly, TARTs exhibit particular adrenal characteristics and were therefore thought to originate from aberrant adrenal cells. More recently, TARTs have been found to also exhibit testicular characteristics. This has led to the hypothesis of pluripotent cells as the origin of TARTs. High concentrations of ACTH could cause hyperplasia of these pluripotent cells, as TARTs appear to be associated with poor hormonal control with concomitant elevated ACTH. Unfortunately, as yet there are no methods to prevent the development of TARTs, nor are there guidelines to treat patients with TARTs. Intensified glucocorticoid treatment could improve fertility status in some cases, although studies report contradicting results. TARTs can also lead to irreversible testicular damage, and therefore semen cryopreservation could be offered to patients with TARTs. Further research should focus on the etiology and pharmacological treatment to prevent TART development or to treat TARTs and improve the fertility status of patients with TARTs.
Copyright © 2019 Endocrine Society.

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Mesh:

Year:  2019        PMID: 30882882     DOI: 10.1210/er.2018-00258

Source DB:  PubMed          Journal:  Endocr Rev        ISSN: 0163-769X            Impact factor:   19.871


  31 in total

1.  Absence of Testicular Adrenal Rest Tumors in Newborns, Infants, and Toddlers with Classical Congenital Adrenal Hyperplasia.

Authors:  Mimi S Kim; Christina M Koppin; Pankhuri Mohan; Fariba Goodarzian; Heather M Ross; Mitchell E Geffner; Roger De Filippo; Paul Kokorowski
Journal:  Horm Res Paediatr       Date:  2019-11-20       Impact factor: 2.852

Review 2.  Clinical and biochemical footprints of inherited metabolic diseases. VIII. Neoplasias.

Authors:  Teodoro Jerves; Nenad Blau; Carlos R Ferreira
Journal:  Mol Genet Metab       Date:  2022-03-28       Impact factor: 4.204

3.  Testicular Adrenal Rest Tumour (TART) or Testicular Malignancy: A Clinical Dilemma.

Authors:  Moni Roy; Ashish Kumar Roy; Tulika Chatterjee; Saurabh Bansal
Journal:  Eur J Case Rep Intern Med       Date:  2020-05-08

Review 4.  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

Review 5.  Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.

Authors:  Hedi L Claahsen-van der Grinten; Phyllis W Speiser; S Faisal Ahmed; Wiebke Arlt; Richard J Auchus; Henrik Falhammar; Christa E Flück; Leonardo Guasti; Angela Huebner; Barbara B M Kortmann; Nils Krone; Deborah P Merke; Walter L Miller; Anna Nordenström; Nicole Reisch; David E Sandberg; Nike M M L Stikkelbroeck; Philippe Touraine; Agustini Utari; Stefan A Wudy; Perrin C White
Journal:  Endocr Rev       Date:  2022-01-12       Impact factor: 19.871

6.  Pituitary corticotroph tumour with adrenocortical cells: A distinct clinicopathologic entity with unique morphology and methylation profile.

Authors:  Richard A Hickman; John T Gionco; Phyllis L Faust; Michael L Miller; Jeffrey Bruce; Gabrielle Page-Wilson; Marc K Rosenblum; Sylvia L Asa
Journal:  Neuropathol Appl Neurobiol       Date:  2021-08-09       Impact factor: 6.250

Review 7.  Management challenges and therapeutic advances in congenital adrenal hyperplasia.

Authors:  Ashwini Mallappa; Deborah P Merke
Journal:  Nat Rev Endocrinol       Date:  2022-04-11       Impact factor: 47.564

8.  Long-term outcome of partial P450 side-chain cleavage enzyme deficiency in three brothers: the importance of early diagnosis.

Authors:  Wafa Kallali; Ewan Gray; Muhammad Zain Mehdi; Robert Lindsay; Louise A Metherell; Federica Buonocore; Jenifer P Suntharalingham; John C Achermann; Malcolm Donaldson
Journal:  Eur J Endocrinol       Date:  2020-03       Impact factor: 6.664

Review 9.  Identifying the deceiver: the non-neoplastic mimickers of genital system neoplasms.

Authors:  Omer Onder; Ali Devrim Karaosmanoglu; Jessica Kraeft; Aycan Uysal; Musturay Karcaaltincaba; Deniz Akata; Mustafa Nasuh Ozmen; Peter F Hahn
Journal:  Insights Imaging       Date:  2021-07-07

10.  Residual Corticosteroid Production in Autoimmune Addison Disease.

Authors:  Åse Bjorvatn Sævik; Anna-Karin Åkerman; Paal Methlie; Marcus Quinkler; Anders Palmstrøm Jørgensen; Charlotte Höybye; Aleksandra J Debowska; Bjørn Gunnar Nedrebø; Anne Lise Dahle; Siri Carlsen; Aneta Tomkowicz; Stina Therese Sollid; Ingrid Nermoen; Kaja Grønning; Per Dahlqvist; Guri Grimnes; Jakob Skov; Trine Finnes; Susanna F Valland; Jeanette Wahlberg; Synnøve Emblem Holte; Katerina Simunkova; Olle Kämpe; Eystein Sverre Husebye; Sophie Bensing; Marianne Øksnes
Journal:  J Clin Endocrinol Metab       Date:  2020-07-01       Impact factor: 5.958

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