21-hydroxylase deficiency differential diagnosis: Difference between revisions
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{| class="wikitable" | {| class="wikitable" | ||
!Disease name | !Disease name | ||
! | !Steroid status | ||
!Other laboratory | |||
! | |||
!Important distinguishing findings | !Important distinguishing findings | ||
|- | |- | ||
|Classic type of 21-hydroxylase deficiency | |Classic type of 21-hydroxylase deficiency | ||
|17-OHP | |Increased: | ||
Progesterone | * 17-OHP | ||
Androstenedione | * Progesterone | ||
DHEA | * Androstenedione | ||
* DHEA | |||
Corticosterone (salt-wasting) | Decreased: | ||
Cortisol (simple virilizing) | * Aldosterone | ||
* Corticosterone (salt-wasting) | |||
* Cortisol (simple virilizing) | |||
| | | | ||
|- | |- | ||
|[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | |[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | ||
|DOC | |Increased: | ||
11-Deoxy- | * DOC | ||
cortisol | * 11-Deoxy- | ||
* cortisol | |||
Corticosterone | Decreased: | ||
Aldosterone | * Cortisol | ||
* Corticosterone | |||
* Aldosterone | |||
| | | | ||
|- | |- | ||
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | |[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | ||
|DOC | |Increased: | ||
Corticosterone | * DOC | ||
Progesterone | * Corticosterone | ||
* Progesterone | |||
Aldosterone | Decreased: | ||
*Cortisol | |||
* Aldosterone | |||
| | | | ||
|- | |- | ||
|3β-Hydroxysteroid Dehydrogenase | |3β-Hydroxysteroid Dehydrogenase | ||
|DHEA | |Increased: | ||
17-OH pregneno-lone | * DHEA | ||
Pregnenolone | * 17-OH pregneno-lone | ||
* Pregnenolone | |||
Aldosterone | Decreased: | ||
* Cortisol | |||
* Aldosterone | |||
| | | | ||
|- | |- | ||
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|- | |- | ||
|Non-classic type of 21-hydroxylase deficiency | |Non-classic type of 21-hydroxylase deficiency | ||
|17-OHP | |Increased: | ||
Exaggerated androstene-dione, DHEA, and 17-OHP | * 17-OHP | ||
response | * Exaggerated androstene-dione, DHEA, and 17-OHP | ||
to ACTH | response to ACTH | ||
| | | | ||
|- | |- | ||
|[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | |[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | ||
|DOC | |Increased: | ||
11-Deoxy- | * DOC | ||
cortisol | * 11-Deoxy- | ||
* cortisol | |||
Corticosterone | Decreased: | ||
Aldosterone | * Cortisol | ||
* Corticosterone | |||
* Aldosterone | |||
| | | | ||
|- | |- | ||
|[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | |[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | ||
|DOC | |Increased: | ||
Corticosterone | * DOC | ||
Progesterone | * Corticosterone | ||
* Progesterone | |||
Aldosterone | Decreased: | ||
*Cortisol | |||
* Aldosterone | |||
| | | | ||
|- | |- | ||
|3β-Hydroxysteroid Dehydrogenase | |3β-Hydroxysteroid Dehydrogenase | ||
|DHEA | |Increased: | ||
17-OH pregneno-lone | * DHEA | ||
Pregnenolone | * 17-OH pregneno-lone | ||
* Pregnenolone | |||
Aldosterone | Decreased: | ||
* Cortisol | |||
* Aldosterone | |||
| | | | ||
|- | |- | ||
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* Polycystic ovaries in sonography | * Polycystic ovaries in sonography | ||
* Obesity | * Obesity | ||
* PCOS is the most common cause of hirsutism in women | |||
* No evidence another diagnosis | |||
|- | |- | ||
|Adrenal tumors | |Adrenal tumors | ||
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| | | | ||
| | | | ||
| | |||
* Older age | |||
* Rapidly progressive symptoms | |||
|- | |- | ||
|Ovarian virilizing tumor | |Ovarian virilizing tumor | ||
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| | | | ||
| | | | ||
| | |||
* Older age | |||
* Rapidly progressive symptoms | |||
|- | |- | ||
|Cushing's syndrome. | |Cushing's syndrome. | ||
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|- | |- | ||
|hyperprolactinemia | |hyperprolactinemia | ||
| | |||
| | | | ||
| | | | ||
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== References == | == References == | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 19:44, 14 July 2017
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters |
Differentiating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
21-hydroxylase deficiency differential diagnosis On the Web |
American Roentgen Ray Society Images of 21-hydroxylase deficiency differential diagnosis |
21-hydroxylase deficiency differential diagnosis in the news |
Directions to Hospitals Treating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
Risk calculators and risk factors for 21-hydroxylase deficiency differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency must be differentiated from 11-β hydroxylase deficiency, 17-α hydroxylase deficiency, androgen insensitivity syndrome, polycystic ovarian syndrome, and adrenal tumor.
Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency classic type must be differentiated from diseases that cause ambiguous genitalia:
Disease name | Steroid status | Other laboratory | Important distinguishing findings |
---|---|---|---|
Classic type of 21-hydroxylase deficiency | Increased:
Decreased:
|
||
11-β hydroxylase deficiency | Increased:
Decreased:
|
||
17-α hydroxylase deficiency | Increased:
Decreased:
|
||
3β-Hydroxysteroid Dehydrogenase | Increased:
Decreased:
|
||
Gestational hyperandrogenism | |||
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Non-classic type must be differentiated from diseases that cause virilization and hirsutism in female:
Disease name | Elevated
Steroids |
Decreased steroids | Androgen status | Important distinguishing findings |
---|---|---|---|---|
Non-classic type of 21-hydroxylase deficiency | Increased:
response to ACTH |
|||
11-β hydroxylase deficiency | Increased:
Decreased:
|
|||
17-α hydroxylase deficiency | Increased:
Decreased:
|
|||
3β-Hydroxysteroid Dehydrogenase | Increased:
Decreased:
|
|||
Polycystic ovary syndrome |
| |||
Adrenal tumors |
| |||
Ovarian virilizing tumor |
| |||
Cushing's syndrome. | ||||
hyperprolactinemia | ||||
Ovarian hyperthecosis | ||||
Syndromes of severe insulin resistance |