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Updated: Jun 7, 2026

Teratoma Generation in the Testis Capsule
Published on: November 7, 2011
[Bilateral testicular tumor in a young man with congenital 11β-hydroxylase deficiency]
Zsolt Vajda1, Gergo Borbély, Zsuzsa Jakab
1Fovárosi Önkormányzat Heim Pál Kórház Budapest Üllői út 86. 1089. zsvajda@heimpalkorhaz.hu
Abstract:
Adrenal rest tumor presenting as palpable testicular mass has been well described in boys and adult males with congenital adrenal hyperplasia. It develops most commonly in patients with 21- hydroxylase deficiency, but the entity may also occur in rare forms of congenital adrenal hyperplasia, including 11β-hydroxylase deficiency. Because the management of testicular adrenal rest tumors is substantially different from that applied in benign and malignant testicular tumors, an accurate differentiation between these entities is particularly important. Authors present the history of a young adult male with 11β-hydroxylase deficiency who developed adrenal rest tumors presenting as palpable bilateral testicular masses during treatment with glucocorticoids, then testicular masses showed a rapid regression after an adequate glucocorticoid treatment. Considering lessons obtained from this case, authors review the pathomechanism, symptoms, as well as current diagnostic and treatment modalities of testicular adrenal rest tumors.
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