AJR Women's Imaging Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Avila, N. A.
Right arrow Articles by Merke, D. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Avila, N. A.
Right arrow Articles by Merke, D. P.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

American Journal of Roentgenology, Vol 172, 1235-1238, Copyright © 1999 by American Roentgen Ray Society


ARTICLES

Testicular adrenal rest tissue in congenital adrenal hyperplasia: serial sonographic and clinical findings

NA Avila, TS Shawker, JV Jones, GB Cutler Jr and DP Merke
Diagnostic Radiology Department, Warren Grant Magnuson Clinical Center, National Institutes of Health, Bethesda, MD 20892-1182, USA.

OBJECTIVE: The purpose of this study was to describe the serial sonographic findings and clinical and laboratory data obtained during follow-up of patients with congenital adrenal hyperplasia in whom testicular adrenal rest tissue develops. MATERIALS AND METHODS: We retrospectively reviewed testicular sonography and laboratory data for 12 patients with congenital adrenal hyperplasia who also had intratesticular masses consistent with adrenal rest tissue. The studies were done during follow-up that ranged from 7 months to 10 years. RESULTS: During follow-up of 11 of the 12 patients after the initial sonographic diagnosis, the testicular adrenal rest tissue either remained stable in size (n = 1), grew larger or smaller (n = 9), disappeared (n = 4), or reappeared after disappearing (n = 3). In one patient, the testicular adrenal rest tissue grew very rapidly in a 1- month interval. Discordant changes in the testicular adrenal rest tissue were noted in 10 patients with bilateral masses. We found no relationship between the change in size of the masses and clinical control (based on 17-hydroxyprogesterone level) at the time of sonography. CONCLUSION: In patients with congenital adrenal hyperplasia who have testicular masses detected sonographically, testicular adrenal rest tissue is the most likely diagnosis. Testicular adrenal rest tissue may remain stable in size, grow larger or smaller, or disappear during sonographic follow-up. The change in size may be marked, may occur very rapidly, and, in our study cohort, was not related to short- term clinical control based on 17-hydroxyprogesterone level at the time of sonography.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Journal of Diagnostic Medical SonographyHome page
N. Kopecky and K. Michael
Testicular Adrenal Rest Tumors Associated With Congenital Adrenal Hyperplasia
Journal of Diagnostic Medical Sonography, January 1, 2008; 24(1): 16 - 19.
[Abstract] [PDF]


Home page
J Ultrasound MedHome page
W. H. Nagamine, S. V. Mehta, and A. Vade
Testicular Adrenal Rest Tumors in a Patient With Congenital Adrenal Hyperplasia: Sonographic and Magnetic Resonance Imaging Findings
J. Ultrasound Med., December 1, 2005; 24(12): 1717 - 1720.
[Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
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., September 1, 2002; 87(9): 4048 - 4053.
[Full Text] [PDF]


Home page
ANN INTERN MEDHome page
D. P. Merke, S. R. Bornstein, N. A. Avila, and G. P. Chrousos
Future Directions in the Study and Management of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Ann Intern Med, February 19, 2002; 136(4): 320 - 334.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
N. M. M. L. Stikkelbroeck, B. J. Otten, A. Pasic, G. J. Jager, C. G. J. F. Sweep, K. Noordam, and A. R. M. M. Hermus
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., December 1, 2001; 86(12): 5721 - 5728.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
M. S. Cabrera, M. G. Vogiatzi, and M. I. New
Long Term Outcome in Adult Males with Classic Congenital Adrenal Hyperplasia
J. Clin. Endocrinol. Metab., July 1, 2001; 86(7): 3070 - 3078.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
P. C. White and P. W. Speiser
Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Endocr. Rev., June 1, 2000; 21(3): 245 - 291.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the American Roentgen Ray Society.