Literature DB >> 18846016

Acromegalic arthropathy of the hip: a case report.

Meltem Alkan Melikoglu1, Ilhan Sezer, Hilal Kocabas, Ali Akdag, Nilufer Balci.   

Abstract

Acromegaly is a chronic and slowly developing endocrinopathy caused by hypersecretion of growth hormone and consequently of insulin like growth factor-1. The arthropathy in acromegaly can affect both axial and peripheral joints and it may present as the earliest clinical symptom of the disease. Patients with acromegaly may have high prevalence of joint related comorbidity and a reduced self perceived quality of life. An early diagnosis is crucial to obtaining the optimal treatment due to the potential reversibility of the lesions in an early stage. The aim of this case report is to draw attention to the possible articular involvement of acromegaly.

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Year:  2008        PMID: 18846016

Source DB:  PubMed          Journal:  Acta Reumatol Port        ISSN: 0303-464X            Impact factor:   1.290


  4 in total

1.  Rheumatoid arthritis masquerading as acromegaly recurrence: report of two cases.

Authors:  Yusuf Aydın; Hülya Coşkun; Seher Kır; Selma Yazici; Özlem Kudaş; Adem Güngör
Journal:  Rheumatol Int       Date:  2010-04-06       Impact factor: 2.631

2.  Clinical and functional outcome of total hip arthroplasty in patients with acromegaly: mean twelve year follow-up.

Authors:  Mustafa Akkaya; Antonio Pignataro; Nemandra Sandiford; Thorsten Gehrke; Mustafa Citak
Journal:  Int Orthop       Date:  2022-05-21       Impact factor: 3.479

Review 3.  Improving Quality of Life in Patients with Pituitary Tumours.

Authors:  Iris Crespo; Alicia Santos; Eugenia Resmini; Elena Valassi; Maria Antonia Martínez-Momblán; Susan M Webb
Journal:  Eur Endocrinol       Date:  2013-03-15

4.  [Destructive arthropathy of the shoulder during an acromegaly].

Authors:  Nessrine Akasbi; Latifa Tahiri; Ouafae Lyhyaoui; Mohammed Elidrissi; Ghita Sqalli Houssaini; Abdelmajid Elmrini; Farida Ajdi; Harzy Taoufik
Journal:  Pan Afr Med J       Date:  2011-10-01
  4 in total

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