Pediatr. praxi 2018; 19(2): 109-112 | DOI: 10.36290/ped.2018.023
In this case study, the authors investigate the condition of a 15,5 year old patient with insulinoma presenting with predominantly neurologicalsymptoms (numbnes in upper limba, lips, and tongue, psychomotor retardation) triggered by recurrent severe hypoglycemia.The initial abdominal ultrasound did not verify any tumorous mass. Subsequent imaging examinations (abdominal ultrasound, endoscopicultrasound, CT, MRI, PET/CT scans, scintigraphy) yielded significantly discrepant results. Only the use of contrast-enhancedendoscopic ultrasonograhy and elastometry identified a small lesion at the junction of the head and the body of the pancreas,non-homogenous in structure with slightly raised echogenicity and discreetly increased blood flow during the contrast-enhancedphase. The elastometry revealed lowered elasticity of the lesion in comparison with the surrounding pancreatic tissue. Based onthese findings, the lesion was suspected to be an insulinoma. Probatory surgical laparotomy was performed, during which a tumorwas identified and successfully removed. Histological findings confirmed a neuroendocrine neoplasia of the insulinoma variety.The patient is currently without neuroglycopenic symptoms, treated as a pediatric endocrinology and gastroenterology outpatient.
Published: May 1, 2018 Show citation
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