Sneddon's Syndrome: Unusual Features and Associations
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Abraheem Abraheem 1 * , Sarah Morcos BA 1
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1 Department of Cardiology, Tameside General Hospital, Tameside and Glossop Foundation Trust, Fountain Street, Ashtonunder- Lyne, OL6 9RW, United Kingdom* Corresponding Author

Abstract

A 43-year-old Caucasian female, with known 46XY chromosome pure gonadal agenesis and systemic hypertension, presented with upper motor neuron weakness of the right face and upper limb. She was also noted to have livedo reticularis and advanced finger clubbing. Left-sided cerebral infarction was confirmed on brain computed tomography (CT) and, following further investigations, a diagnosis of Sneddon’s s syndrome (SS) was made. Three years later, she went on to develop adenocarcinoma of the right lung, which sadly claimed her life within 4 months. To our knowledge, this is the first reported case of SS in association with finger clubbing and pure gonadal agenesis.

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Article Type: Case Report

EUR J GEN MED, 2011, Volume 8, Issue 3, 240-242

https://doi.org/10.29333/ejgm/82746

Publication date: 11 Jul 2011

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