Publications by authors named "Candelaria Serrano"

Article Synopsis
  • * A case report details a 59-year-old woman who developed nosebleeds and other symptoms resembling Hereditary Hemorrhagic Telangiectasia (HHT) after starting T-DM1 treatment, despite no prior HHT history.
  • * Treatment measures included nasal care and prescription of propranolol, which effectively reduced symptoms, highlighting the need for oncologists to recognize and manage this rare side effect of T-DM1.
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Introduction: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular dysplasia that might affect 1/5000-10 000 individuals worldwide. It is a rare and underdiagnosed condition. Population-based epidemiological studies are crucial for comprehending and quantifying the impact of this disease.

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The bilateral presentation of peritonsillar abscess is uncommon. Its management is controversial and it has been argued whether a quinsy tonsillectomy or an interval tonsillectomy should be performed. Here we describe the case of a 14-year-old boy with sore throat, trismus, and fever.

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