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Srpski arhiv za celokupno lekarstvo 2007 Volume 135, Issue 5-6, Pages: 326-329
https://doi.org/10.2298/SARH0706326M
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Benign solitary fibrous pleural tumor and hypoglycaemia

Milenković Branislava (Institut za plućne bolesti i tuberkulozu, Klinički centar Srbije, Beograd)
Stojšić Jelena ORCID iD icon (Institut za plućne bolesti i tuberkulozu, Klinički centar Srbije, Beograd)
Dudvarski Aleksandra (Institut za plućne bolesti i tuberkulozu, Klinički centar Srbije, Beograd)
Bošnjak-Petrović Vesna (Institut za plućne bolesti i tuberkulozu, Klinički centar Srbije, Beograd)
Ercegovac Maja (Institut za plućne bolesti i tuberkulozu, Klinički centar Srbije, Beograd)

Introduction: Solitary fibrous tumors of the pleura are uncommon and discovered fortuitously or in patients with non-specific respiratory symptoms. When associated with hypoglycaemia, they are commonly referred to as Doege-Potter syndrome. Case outline. A 68-year old woman presented with a large pleural mass. She had a long history of headache and decreased consciousness with one-year worsening dyspnoea and right-sided chest pain. The chest X-ray revealed an enormous opacity occupying almost the entire right hemithorax. Endocrine tests showed an extremely reduced glucose level and blood concentration of insulin, C-peptide, glucagon, growth hormone and catecholamines within normal range. After fine-needle aspiration, by histological and immunohistochemical analysis, a benign solitary fibrous pleural tumor was diagnosed. Although surgical resection of such a huge tumor with hypoglycaemia is usually curative, our patient declined surgery and opted for conservative treatment with intravenous glucose. Conclusion. Clinicians should be aware of this rare, but important cause of hypoglycaemia and exclude a fibrous pleural tumor in the assessment of their patients. .

Keywords: solitary fibrous pleural tumors, hypoglycaemia, Doege-Potter syndrome

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