Occult Nesidioblastosis Detected by 111In-Pentetreotide Single-Photon Emission Computed Tomography.
Autor: | Sakamoto S; Department of Gastroenteorlogical Surgery, Kochi Health Sciences Center., Tabuchi M; Department of Gastroenteorlogical Surgery, Kochi Health Sciences Center., Yoshimatsu R; Department of Radiology, Kochi Health Sciences Center., Hishida A; Department of Endocrinology and Metabolism, Kochi Health Sciences Center., Matsumoto M; Department of Diagnostic Pathology, Kochi Health Sciences Center., Iwata J; Department of Diagnostic Pathology, Kochi Health Sciences Center., Okabayashi T; Department of Gastroenteorlogical Surgery, Kochi Health Sciences Center. |
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Jazyk: | angličtina |
Zdroj: | Acta medica Okayama [Acta Med Okayama] 2024 Oct; Vol. 78 (5), pp. 423-428. |
DOI: | 10.18926/AMO/67667 |
Abstrakt: | Nesidioblastosis, also known as persistent hyperinsulinemic hypoglycemia, is usually observed in children and infants, although more recently adult-onset nesidioblastosis has also been described. We present a case of nesidioblastosis in a 78-year-old man that was detected by 111In-pentetreotide single photon emission computed tomography (SPECT/CT). The patient was transferred to our hospital's emergency department in a hypoglycemic coma. Dynamic enhanced CT could detect no lesion in the pancreas, but an 111In-pentetreotide SPECT/CT scan performed after a similar episode four weeks later showed increased focal uptake at the head of the pancreas. The results of a selective arterial calcium injection test were negative. After careful consideration and discussion among colleagues, surgical intervention was selected, and a pancreaticoduodenectomy was performed. On histology, there were elevated numbers of Langerhans islets in the pancreatic head, and the islets themselves appeared enlarged. Hypertrophic β-cells comprised the majority, but α-cells, δ-cells and pancreatic polypeptide were also detected in the islets. Based on the histopathological results and repeated hyperinsulinemic hypoglycemic crises, the patient was finally diagnosed with adult-onset nesidioblastosis. He had no hypoglycemic symptoms during outpatient follow-up examination. Since 111In-pentetreotide SPECT/CT may be able to detect nesidioblastosis, clinicians should consider this relatively new-modality examination when encountering such cases. Competing Interests: No potential conflict of interest relevant to this article was reported. |
Databáze: | MEDLINE |
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