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        <identifier>oai:figshare.com:article/34022637</identifier>
        <datestamp>2026-09-29T10:30:00Z</datestamp>
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          <dc:title>Supplemental Material for: Marked hypokalemia at presentation in an adolescent with ectopic ACTH syndrome secondary to a bronchial carcinoid tumor: a case report</dc:title>
          <dc:creator>figshare admin karger (2628495)</dc:creator>
          <dc:creator>Hasan Yanik (25136594)</dc:creator>
          <dc:creator>Asli Derya Kardelen (25136597)</dc:creator>
          <dc:creator>Dogu Vuralli Bakkaloglu (25136600)</dc:creator>
          <dc:creator>Zeynep Gozde Ozkan (25136602)</dc:creator>
          <dc:creator>Salih Duman (24776749)</dc:creator>
          <dc:creator>Berker Ozkan (25136605)</dc:creator>
          <dc:creator>Melek Yildiz (13361952)</dc:creator>
          <dc:creator>Sukran Poyrazoglu (25136609)</dc:creator>
          <dc:creator>Firdevs Bas (16994462)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;Introduction: Ectopic ACTH syndrome (EAS) is a rare cause of Cushing's syndrome in children and adolescents, accounting for less than 1% of pediatric cases. Compared with Cushing's disease, EAS follows a more rapid clinical course with more pronounced metabolic disturbances, among which hypokalemia is one of the most distinctive features.&lt;/p&gt;&lt;p dir="ltr"&gt;Case Presentation: A 14.7-year-old male presented with a three-month history of rapid weight gain, violaceous striae, hypertension, and proximal muscle weakness. Markedhypokalemia (2.8 mmol/L) prompted endocrine work-up, which revealed ACTH-dependent hypercortisolism with loss of diurnal cortisol rhythm, elevated midnight salivary cortisol, and non-suppression on low- and high-dose dexamethasone suppression tests. Pituitary MRI was unremarkable, and the marked hypokalemia raised suspicion of an ectopic source. Thoracic CT identified a nodular lesion in the right middle lobe, with corresponding uptake on ⁶⁸Ga-DOTATATE PET/CT. Right middle lobectomy was performed, and histopathology confirmed a typical bronchial carcinoid tumor. Postoperatively, hypercortisolism resolved, electrolyte balance normalized, and Cushingoid features regressed.&lt;/p&gt;&lt;p dir="ltr"&gt;Conclusion:Markedhypokalemia at presentation may serve as an early biochemical clue to ectopic ACTH secretion in pediatric ACTH-dependent hypercortisolism, and should prompt timely evaluation for extrapituitary sources, including bronchial carcinoid tumors.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-29T10:30:00Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.34022637.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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