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J Clin Endocrinol Metab ; 97(6): E963-7, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22466332

ABSTRACT

CONTEXT: Hyperinsulinemic hypoglycemia after Roux-en-Y gastric bypass (RYGB) has been increasingly reported. It is induced by ß-cell hyperplasia often referred to as nesidioblastosis. Positron emission tomography (PET) with [11C]-5-hydroxytryptophan ((11)C-HTP) and 6-[18F]fluoro-3,4-dihydroxy-l-phenylalanine ((18)F-DOPA) has been successfully applied to image neuroendocrine tumors. No data are available of the usefulness of these functional imaging techniques in post-RYGB in this new endocrine disorder, neither for diagnostic purposes nor for follow-up. OBJECTIVE: We present a patient with post-RYGB hypoglycemia who underwent (11)C-HTP and (18)F-DOPA PET scintigraphy for diagnostic purposes and to evaluate the effect of additional laparoscopic adjustable banding of the pouch as a surgical therapy for this disorder. PATIENT: We describe a woman with biochemically confirmed post-RYGB hypoglycemia who showed diffuse uptake of the (11)C-HTP and (18)F-DOPA tracers in the entire pancreas. After failure of dietary and medical treatment options, she underwent a laparoscopic adjustable banding for pouch dilatation. Subjective improvement was noted, which coincided with decreased uptake of (18)F-DOPA and (11)C-HTP in the head of the pancreas. CONCLUSIONS: Functional imaging by (18)F-DOPA- and (11)C-HTP-PET can accurately visualize diffuse endocrine pancreatic activity in post-gastric bypass hyperinsulinemic hypoglycemia. Both (11)C-HTP- and (18)F-DOPA-PET imaging appear to have a similar diagnostic performance in the presented case, and uptake of both tracers potentially relates to disease activity after surgical intervention.


Subject(s)
Gastric Bypass/adverse effects , Hypoglycemia/diagnostic imaging , Obesity, Morbid/surgery , Positron-Emission Tomography/methods , Postoperative Complications/diagnostic imaging , Adult , Carbon Radioisotopes , Dihydroxyphenylalanine/analogs & derivatives , Female , Fluorodeoxyglucose F18 , Humans , Hyperinsulinism/diagnostic imaging , Hyperinsulinism/etiology , Hypoglycemia/etiology , Nesidioblastosis/diagnostic imaging , Nesidioblastosis/etiology
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