A rare cause of acromegaly: McCune-Albright syndrome
McCune-Albright syndrome is characterized by polyostatic fibrous dysplasia, brown spots on the skin (café au lait pigmentation) and autonomous endocrine hyperfunction. Early puberty and other endocrinological manifestations, such as acromegaly, gigantism and hypercortisolism are widely observed in...
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Dicle University Medical School
2015-06-01
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doaj-ccb45a68da324c01b0bf768e97a9a7962020-11-24T23:44:23ZengDicle University Medical SchoolDicle Medical Journal 1300-29451308-98892015-06-0142224224410.5798/diclemedj.0921.2015.02.0564A rare cause of acromegaly: McCune-Albright syndromeErdal Bodakçi 0Mazhar Müslüm Tuna 1Faruk Kılınç 2Zafer Pekkolay 3Hikmet Soylu 4Şadiye Altun Tuzcu 5Alpaslan Kemal Tuzcu 6Dicle Üniversitesi Tıp Fakültesi İç Hastalıkları Anabilim Dalı, Diyarbakır, Türkiye Dicle Üniversitesi Tıp Fakültesi Endokrinoloji ve Metabolizma Bilim Dalı, Diyarbakır , Türkiye Dicle Üniversitesi Tıp Fakültesi Endokrinoloji ve Metabolizma Bilim Dalı, Diyarbakır , Türkiye Dicle Üniversitesi Tıp Fakültesi Endokrinoloji ve Metabolizma Bilim Dalı, Diyarbakır , Türkiye Dicle Üniversitesi Tıp Fakültesi Endokrinoloji ve Metabolizma Bilim Dalı, Diyarbakır , TürkiyeDiyarbakır Eğitim ve Araştırma Hastanesi Nükleer Tıp Kliniği, Diyarbakır, Türkiye Dicle Üniversitesi Tıp Fakültesi Endokrinoloji ve Metabolizma Bilim Dalı, Diyarbakır , Türkiye McCune-Albright syndrome is characterized by polyostatic fibrous dysplasia, brown spots on the skin (café au lait pigmentation) and autonomous endocrine hyperfunction. Early puberty and other endocrinological manifestations, such as acromegaly, gigantism and hypercortisolism are widely observed in the syndrome. Acromegaly is seen in 20% of patients. We report a case of acromegaly accompanied with this syndrome.http://www.diclemedj.org/upload/sayi/36/Dicle%20Med%20J-02416.pdfMcCune-Albright syndrome; acromegaly; fi - brous dysplasia |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Erdal Bodakçi Mazhar Müslüm Tuna Faruk Kılınç Zafer Pekkolay Hikmet Soylu Şadiye Altun Tuzcu Alpaslan Kemal Tuzcu |
spellingShingle |
Erdal Bodakçi Mazhar Müslüm Tuna Faruk Kılınç Zafer Pekkolay Hikmet Soylu Şadiye Altun Tuzcu Alpaslan Kemal Tuzcu A rare cause of acromegaly: McCune-Albright syndrome Dicle Medical Journal McCune-Albright syndrome; acromegaly; fi - brous dysplasia |
author_facet |
Erdal Bodakçi Mazhar Müslüm Tuna Faruk Kılınç Zafer Pekkolay Hikmet Soylu Şadiye Altun Tuzcu Alpaslan Kemal Tuzcu |
author_sort |
Erdal Bodakçi |
title |
A rare cause of acromegaly: McCune-Albright syndrome |
title_short |
A rare cause of acromegaly: McCune-Albright syndrome |
title_full |
A rare cause of acromegaly: McCune-Albright syndrome |
title_fullStr |
A rare cause of acromegaly: McCune-Albright syndrome |
title_full_unstemmed |
A rare cause of acromegaly: McCune-Albright syndrome |
title_sort |
rare cause of acromegaly: mccune-albright syndrome |
publisher |
Dicle University Medical School |
series |
Dicle Medical Journal |
issn |
1300-2945 1308-9889 |
publishDate |
2015-06-01 |
description |
McCune-Albright syndrome is characterized by polyostatic fibrous dysplasia, brown spots on the skin (café au lait pigmentation) and autonomous endocrine hyperfunction. Early puberty and other endocrinological manifestations, such as acromegaly, gigantism and hypercortisolism are widely observed in the syndrome. Acromegaly is seen in 20% of patients. We report a case of acromegaly accompanied with this syndrome. |
topic |
McCune-Albright syndrome; acromegaly; fi - brous dysplasia |
url |
http://www.diclemedj.org/upload/sayi/36/Dicle%20Med%20J-02416.pdf |
work_keys_str_mv |
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