Literature DB >> 3698500

Computed tomography in untreated adults with virilizing congenital adrenal cortical hyperplasia.

T H Falke, A P van Seters, A Schaberg, A J Moolenaar.   

Abstract

Thirteen adult patients with biochemically proven congenital adrenal hyperplasia (CAH) were examined by computed tomography (CT). Six patients had never received glucocorticoid therapy. In three of those six patients, CT revealed a tumorous transformation in one of the hyperplastic adrenal glands. In the seven patients with CAH who were treated since childhood, no mass could be demonstrated on CT. The development of an adrenocortical tumour due to chronic adrenal cortical stimulation by excessive adreno-cortico-trophic hormone (ACTH) production in adult patients with untreated CAH may not be a rare occurrence, as is demonstrated in this series. It is important not to confuse this entity with a primary virilizing adrenal tumour which requires a different form of treatment. In case of tumorous transformation in untreated adults with CAH, suppressive therapy with CT control should be favoured over surgery, as long as the tumour is ACTH-dependent. Moreover, these observations illustrate the desirability of lifelong glucocorticoid therapy in patients with CAH, including adult males who biochemically may not require suppression of steroid androgen excess.

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Year:  1986        PMID: 3698500     DOI: 10.1016/s0009-9260(86)80389-0

Source DB:  PubMed          Journal:  Clin Radiol        ISSN: 0009-9260            Impact factor:   2.350


  8 in total

1.  Computed tomography in untreated congenital adrenal hyperplasia.

Authors:  C V Harinarayana; G Renu; A C Ammini; M L Khurana; P Ved; M G Karmarkar; M M Ahuja; M Berry
Journal:  Pediatr Radiol       Date:  1991

2.  Imaging of congenital lipoid adrenal hyperplasia.

Authors:  Ehiichi Kohda; Hiroya Yamazaki; Hiromi Hisazumi; Yoshiyuki Tutumi; Tsutomu Ogata; Nobuyuki Shiraga
Journal:  Radiat Med       Date:  2006-04

3.  Clinical manifestations and hormonal profile of two women with Cushing's disease and mild deficiency of 21-hydroxylase.

Authors:  M Boronat; A Carrillo; A Ojeda; J Estrada; B Ezquieta; F Marín; F J Nóvoa
Journal:  J Endocrinol Invest       Date:  2004-06       Impact factor: 4.256

4.  Adrenal mass with virilisation: importance of endocrine investigation.

Authors:  J Nasir; C Walton
Journal:  BMJ       Date:  1996-10-05

Review 5.  Prostate gland development and adrenal tumor in a female with congenital adrenal hyperplasia: a case report and review from radiology perspective.

Authors:  Benjamin Fang; Francis Cho; Wendy Lam
Journal:  J Radiol Case Rep       Date:  2013-12-01

6.  Macronodular congenital adrenal hyperplasia in an adult with female pseudohermaphroditism.

Authors:  A M Norris; J B O'Driscoll; H Mamtora
Journal:  Eur Radiol       Date:  1996       Impact factor: 5.315

7.  NONCLASSICAL 21-HYDROXYLASE DEFICIENCY PRESENTED AS ADDISON'S DISEASE AND BILATERAL ADRENAL INCIDENTALOMAS.

Authors:  X Meng; Y Yu
Journal:  Acta Endocrinol (Buchar)       Date:  2017 Apr-Jun       Impact factor: 0.877

8.  Untreated Congenital Adrenal Hyperplasia with 17-α Hydroxylase/17,20-Lyase Deficiency Presenting as Massive Adrenocortical Tumor.

Authors:  Su Jin Lee; Je Eun Song; Sena Hwang; Ji Yeon Lee; Hye Sun Park; Seunghee Han; Yumie Rhee
Journal:  Endocrinol Metab (Seoul)       Date:  2015-08-04
  8 in total

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