A Case of Wilson’s Disease Mimicking Malignancy

Wilson’s disease is a rare autosomal recessive inherited disorder of copper metabolism that causes various degrees of hepatic and neuropsychiatric symptoms. The condition is due to mutations in the ATP7B gene localized to arm 13q. The clinical signs are complex. The accumulation of copper in the bra...

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Main Authors: Ahmet Akın, Şakir Özgür Keşkek, Mehmet Aliustaoğlu, Nedime Şahinoğlu-Keşkek
Format: Article
Language:English
Published: Galenos Yayinevi 2014-03-01
Series:Haseki Tıp Bülteni
Subjects:
Online Access:http://www.hasekidergisi.com/article_4735/A-Case-Of-Wilsons-Disease-Mimicking-Malignancy
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author Ahmet Akın
Şakir Özgür Keşkek
Mehmet Aliustaoğlu
Nedime Şahinoğlu-Keşkek
author_facet Ahmet Akın
Şakir Özgür Keşkek
Mehmet Aliustaoğlu
Nedime Şahinoğlu-Keşkek
author_sort Ahmet Akın
collection DOAJ
description Wilson’s disease is a rare autosomal recessive inherited disorder of copper metabolism that causes various degrees of hepatic and neuropsychiatric symptoms. The condition is due to mutations in the ATP7B gene localized to arm 13q. The clinical signs are complex. The accumulation of copper in the brain causes tremor, dysartria and psychiatric problems. The deposits in the liver can lead to acute, chronic and progressive hepatitis and cirrhosis. Wilson’s disease is the first liver disease for which an effective pharmacological treatment was found. In this paper, we gave particular importance to liver involvement in Wilson’s disease and emphasized that the disease can be confused with metastatic liver diseases. (The Me­di­cal Bul­le­tin of Ha­se­ki 2014; 52: 64-6)
first_indexed 2024-04-10T14:47:21Z
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2147-2688
language English
last_indexed 2024-04-10T14:47:21Z
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publisher Galenos Yayinevi
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spelling doaj.art-e1461a15f70743f281d813dec28e1de92023-02-15T16:07:46ZengGalenos YayineviHaseki Tıp Bülteni1302-00722147-26882014-03-01521646610.4274/Haseki.1297A Case of Wilson’s Disease Mimicking MalignancyAhmet Akın0Şakir Özgür Keşkek1Mehmet Aliustaoğlu2Nedime Şahinoğlu-Keşkek3Dr. Lütfi Kırdar Kartal Eğitim ve Araştırma Hastanesi, Dahiliye Kliniği, İstanbul, TürkiyeNumune Eğitim ve Araştırma Hastanesi, Dahiliye Kliniği, Adana, TürkiyeDr. Lütfi Kırdar Kartal Eğitim ve Araştırma Hastanesi, Dahiliye Kliniği, İstanbul, TürkiyeNumune Eğitim ve Araştırma Hastanesi, Göz Hastalıkları Kliniği, Adana, TürkiyeWilson’s disease is a rare autosomal recessive inherited disorder of copper metabolism that causes various degrees of hepatic and neuropsychiatric symptoms. The condition is due to mutations in the ATP7B gene localized to arm 13q. The clinical signs are complex. The accumulation of copper in the brain causes tremor, dysartria and psychiatric problems. The deposits in the liver can lead to acute, chronic and progressive hepatitis and cirrhosis. Wilson’s disease is the first liver disease for which an effective pharmacological treatment was found. In this paper, we gave particular importance to liver involvement in Wilson’s disease and emphasized that the disease can be confused with metastatic liver diseases. (The Me­di­cal Bul­le­tin of Ha­se­ki 2014; 52: 64-6)http://www.hasekidergisi.com/article_4735/A-Case-Of-Wilsons-Disease-Mimicking-MalignancyWilson’s diseasemalignancyliver
spellingShingle Ahmet Akın
Şakir Özgür Keşkek
Mehmet Aliustaoğlu
Nedime Şahinoğlu-Keşkek
A Case of Wilson’s Disease Mimicking Malignancy
Haseki Tıp Bülteni
Wilson’s disease
malignancy
liver
title A Case of Wilson’s Disease Mimicking Malignancy
title_full A Case of Wilson’s Disease Mimicking Malignancy
title_fullStr A Case of Wilson’s Disease Mimicking Malignancy
title_full_unstemmed A Case of Wilson’s Disease Mimicking Malignancy
title_short A Case of Wilson’s Disease Mimicking Malignancy
title_sort case of wilson s disease mimicking malignancy
topic Wilson’s disease
malignancy
liver
url http://www.hasekidergisi.com/article_4735/A-Case-Of-Wilsons-Disease-Mimicking-Malignancy
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