Literature DB >> 14612605

"Osler's phenomenon": misdiagnosing Cushing's syndrome.

P De1, L M Evans, M F Scanlon, J S Davies.   

Abstract

The clinical manifestations of Cushing's syndrome can be quite variable and are frequently mistaken, with consequent delayed diagnosis and significant morbidity and mortality. Harvey Cushing described the typical signs and symptoms of Cushing's syndrome but unfortunately attributed the features to myxoedema. The first typical description of a patient with Cushing's syndrome was probably made by Sir William Osler in 1898. Thus delay or misdiagnosis with consequent high morbidity and mortality exemplifies the history of Cushing's syndrome. Four cases of Cushing's syndrome are described that were associated with deteriorating morbidity because of the considerable delay from first presentation to a secondary care physician to eventual diagnosis. The clinical diagnosis was delayed in all the four patients, although they had symptoms and signs that were missed by a number of primary and secondary care physicians. Trans-sphenoidal surgery resulted in biochemical cure as well as improvement in the accompanying co-morbidity. Although still rare, the prevalence of Cushing's syndrome is increasing. Increasing clinical awareness and the use of appropriate screening tests should facilitate earlier diagnosis with reduced morbidity and mortality. Although the syndrome is named after Harvey Cushing, Sir William Osler was probably the first to describe it. Therefore, in deference to Osler's contribution to Cushing's syndrome and the work of Harvey Cushing, it is suggested that to the list of the other eponymous conditions of Osler-Weber-Rendu and Osler's nodes, should be added the delay or misdiagnosis of Cushing's syndrome-"Osler's phenomenon".

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Year:  2003        PMID: 14612605      PMCID: PMC1742858          DOI: 10.1136/pmj.79.936.594

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


  5 in total

Review 1.  Cushing's syndrome: why is diagnosis so difficult?

Authors:  David C Aron
Journal:  Rev Endocr Metab Disord       Date:  2010-06       Impact factor: 6.514

2.  A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study.

Authors:  Paola Pierucci; Gennaro M Lenato; Patrizia Suppressa; Patrizia Lastella; Vincenzo Triggiani; Raffaella Valerio; Mario Comelli; Daniela Salvante; Alessandro Stella; Nicoletta Resta; Giancarlo Logroscino; Francesco Resta; Carlo Sabbà
Journal:  Orphanet J Rare Dis       Date:  2012-06-07       Impact factor: 4.123

3.  Treatment Options in Cushing's Disease.

Authors:  Ahmed Rizk; Juergen Honegger; Monika Milian; Tsambika Psaras
Journal:  Clin Med Insights Oncol       Date:  2012-01-11

4.  Targeting under-diagnosis in hereditary hemorrhagic telangiectasia: a model approach for rare diseases?

Authors:  Giuseppe A Latino; Dale Brown; Richard H Glazier; Jonathan T Weyman; Marie E Faughnan
Journal:  Orphanet J Rare Dis       Date:  2014-07-25       Impact factor: 4.123

5.  William Osler and Harvey Williams Cushing: Friendship Around Neurosurgery.

Authors:  Marleide da Mota Gomes
Journal:  Ann Indian Acad Neurol       Date:  2019-10-25       Impact factor: 1.383

  5 in total

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