18 April 2025
: Case report
Diagnostic and Surgical Management of Nesidioblastosis in a 42-Year-Old Man with Refractory Hypoglycemia
Challenging differential diagnosis, Unusual or unexpected effect of treatment, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)
Cleomar Ana de Souza ValentimDOI: 10.12659/AJCR.945453
Am J Case Rep 2025; 26:e945453
Table 1. Biochemical and imaging tests.
| Test | Result | Reference range | |
|---|---|---|---|
| Insulin | 1.30 | 2.6–24.9 µIU/ml | |
| C-peptide | 0.90 | 1.1–4.4 ng/ml | |
| Pro-insulin | 4.99 | 0.7–4.30 pmol/l | |
| Insulin | 624.8 | 2.6–24.9 µIU/ml | |
| C-peptide | 0.30 | 1.1–4.4 ng/ml | |
| AB anti-insulin | 5.80 | <10 U/ml | |
| CT – computed tomography; PET – positron emission tomography; UVJ – ureterovesical junction; UPJ – ureteropelvic junction; AB – antibodies. | |||
| Imaging method | Result | ||
| Abdominal CT + kidneys and urinary tract | Ureteral microlithiasis - UVJ on the right, determining mild hydroureteronephrosis. Hepatic steatosis, nephrolithiasis on the left (Calculus in the UPJ 7 mm and calices in the upper pole 1,3cm), without obstructive appearance. Small umbilical hernia | ||
| No evidence of a well-differentiated neuroendocrine neoplasm detectable by the method, thus impairing confirmation of the hypothesis of insulinoma | |||
| Upper echo-endoscopy | Absence of pancreatic or peripancreatic lesions suspicious of insulinoma. Absence of lymph node enlargement in the chains studied | ||
| No evidence of detectable hypermetabolic foci under the present conditions | |||
| Pathological anatomy | Pancreatic parenchyma is within normal standards. Congestive splenomegaly. Note: Some islets of Langhans show slight hypercellularity. Clinical suspicion: Nesideoblastosis | ||
| CT – computed tomography; PET – positron emission tomography; UVJ – ureterovesical junction; UPJ – ureteropelvic junction; AB – antibodies. | |||






