Surgical Management, Preoperative Tumor Localization, and Histopathology of 80 Patients Operated on for Insulinoma

Author:

Andreassen Mikkel12ORCID,Ilett Emma12,Wiese Dominik34,Slater Emily P34,Klose Marianne12,Hansen Carsten Palnæs25,Gercke Norman34,Langer Seppo W26,Kjaer Andreas27,Maurer Elisabeth34,Federspiel Birgitte28,Kann Peter H39,Bartsch Detlef K34,Knigge Ulrich125

Affiliation:

1. Department of Endocrinology Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

2. European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark

3. European Neuroendocrine Tumor Society, Philipps University, Marburg, Germany

4. Department of Visceral, Thoracic and Vascular Surgery, Philipps University, Marburg, Germany

5. Department of Surgery, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

6. Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

7. Department of Clinical Physiology, Nuclear Medicine, & PET and Cluster for Molecular Imaging, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

8. Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

9. Department of Gastroenterology and Division of Endocrinology, Philipps University, Marburg, Germany

Abstract

AbstractIntroductionDiagnosis and pathological classification of insulinomas are challenging.AimTo characterize localization of tumors, surgery outcomes, and histopathology in patients with insulinoma.MethodsPatients with surgically resected sporadic insulinoma were included.ResultsEighty patients were included. Seven had a malignant tumor. A total of 312 diagnostic examinations were performed: endoscopic ultrasonography (EUS; n = 59; sensitivity, 70%), MRI (n = 33; sensitivity, 58%), CT (n = 55; sensitivity, 47%), transabdominal ultrasonography (US; n = 45; sensitivity, 40%), somatostatin receptor imaging (n = 17; sensitivity, 29%), 18F-fluorodeoxyglucose positron emission tomography/CT (n = 1; negative), percutaneous transhepatic venous sampling (n = 10; sensitivity, 90%), arterial stimulation venous sampling (n = 20; sensitivity, 65%), and intraoperative US (n = 72; sensitivity, 89%). Fourteen tumors could not be visualized. Invasive methods were used in 7 of these 14 patients and localized the tumor in all cases. Median tumor size was 15 mm (range, 7 to 80 mm). Tumors with malignant vs benign behavior showed less staining for insulin (3 of 7 vs 66 of 73; P = 0.015) and for proinsulin (3 of 6 vs 58 of 59; P < 0.001). Staining for glucagon was seen in 2 of 6 malignant tumors and in no benign tumors (P < 0.001). Forty-three insulinomas stained negative for somatostatin receptor subtype 2a.ConclusionLocalization of insulinomas requires many different diagnostic procedures. Most tumors can be localized by conventional imaging, including EUS. For nonvisible tumors, invasive methods may be a useful diagnostic tool. Malignant tumors showed reduced staining for insulin and proinsulin and increased staining for glucagon.

Funder

Krftens Bekmpelse

Arvid Nilssons Fond

Det Sundhedsvidenskabelige Fakultet, Kbenhavns Universitet

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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