Acromegaly history and symptoms: Difference between revisions

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{{Acromegaly}}
{{Acromegaly}}
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==Symptoms==
==Overview==
==History and Symptoms==
Features that result from high level of hGH or expanding tumor include:
Features that result from high level of hGH or expanding tumor include:
* Soft tissue swelling of the hands and feet
* Soft tissue swelling of the hands and feet
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==Pituitary gigantism in children==
===Pituitary gigantism in children===
This condition of growth hormone excess is rare in children and is referred to as [[gigantism|pituitary gigantism]], because the excessive growth hormone produces excessive growth of bones and the child can achieve excessive height. As an affected child becomes an adult, many of the adult problems can gradually develop. The distinction between gigantism (occurring in children) and acromegaly (occurring in adults) can be made by the occurrence of the adenoma in relation to the closure of the [[Bone#Formation|epiphyses]]. If elevated growth hormone levels occur before the closure of the epiphyses (i.e. in prepubertal children), then gigantism ensues. If it occurs after the closure of the epiphyses (i.e., in adults) then acromegaly ensues.
This condition of growth hormone excess is rare in children and is referred to as [[gigantism|pituitary gigantism]], because the excessive growth hormone produces excessive growth of bones and the child can achieve excessive height. As an affected child becomes an adult, many of the adult problems can gradually develop. The distinction between gigantism (occurring in children) and acromegaly (occurring in adults) can be made by the occurrence of the adenoma in relation to the closure of the [[Bone#Formation|epiphyses]]. If elevated growth hormone levels occur before the closure of the epiphyses (i.e. in prepubertal children), then gigantism ensues. If it occurs after the closure of the epiphyses (i.e., in adults) then acromegaly ensues.
==References==
==References==


{{reflist|2}}
{{reflist|2}}
[[Category:neuroendocrinology]]
[[Category:Growth disorders]]
[[Category:Growth hormones]]
[[Category:Endocrinology]]
[[bg:Акромегалия]]
[[cs:Akromegalie]]
[[de:Akromegalie]]
[[es:Acromegalia]]
[[fr:Acromégalie]]
[[gl:Acromegalia]]
[[it:Acromegalia]]
[[he:אקרומגליה]]
[[nl:Acromegalie]]
[[ja:先端巨大症]]
[[no:Akromegali]]
[[pl:Akromegalia]]
[[pt:Acromegalia]]
[[sq:Akromegalia]]
[[sk:Akromegália]]
[[sr:Акромегалија]]
[[fi:Akromegalia]]
[[sv:Akromegali]]
[[tr:Akromegali]]
[[uk:Акромегалія]]
[[zh:肢端肥大症]]
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Revision as of 19:41, 31 August 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

History and Symptoms

Features that result from high level of hGH or expanding tumor include:


(Image courtesy of Charlie Goldberg, M.D., UCSD School of Medicine and VA Medical Center, San Diego, California)

Pituitary gigantism in children

This condition of growth hormone excess is rare in children and is referred to as pituitary gigantism, because the excessive growth hormone produces excessive growth of bones and the child can achieve excessive height. As an affected child becomes an adult, many of the adult problems can gradually develop. The distinction between gigantism (occurring in children) and acromegaly (occurring in adults) can be made by the occurrence of the adenoma in relation to the closure of the epiphyses. If elevated growth hormone levels occur before the closure of the epiphyses (i.e. in prepubertal children), then gigantism ensues. If it occurs after the closure of the epiphyses (i.e., in adults) then acromegaly ensues.

References

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