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


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 12 2019
Historique:
received: 27 05 2019
accepted: 26 07 2019
pubmed: 2 8 2019
medline: 29 5 2020
entrez: 2 8 2019
Statut: ppublish

Résumé

Diagnosis and pathological classification of insulinomas are challenging. To characterize localization of tumors, surgery outcomes, and histopathology in patients with insulinoma. Patients with surgically resected sporadic insulinoma were included. Eighty 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. Localization 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.

Identifiants

pubmed: 31369096
pii: 5540966
doi: 10.1210/jc.2019-01204
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6129-6138

Informations de copyright

Copyright © 2019 Endocrine Society.

Auteurs

Mikkel Andreassen (M)

Department of Endocrinology Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.

Emma Ilett (E)

Department of Endocrinology Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.

Dominik Wiese (D)

European Neuroendocrine Tumor Society, Philipps University, Marburg, Germany.
Department of Visceral, Thoracic and Vascular Surgery, Philipps University, Marburg, Germany.

Emily P Slater (EP)

European Neuroendocrine Tumor Society, Philipps University, Marburg, Germany.
Department of Visceral, Thoracic and Vascular Surgery, Philipps University, Marburg, Germany.

Marianne Klose (M)

Department of Endocrinology Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.

Carsten Palnæs Hansen (CP)

European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.
Department of Surgery, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Norman Gercke (N)

European Neuroendocrine Tumor Society, Philipps University, Marburg, Germany.
Department of Visceral, Thoracic and Vascular Surgery, Philipps University, Marburg, Germany.

Seppo W Langer (SW)

European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.
Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Andreas Kjaer (A)

European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.
Department of Clinical Physiology, Nuclear Medicine, & PET and Cluster for Molecular Imaging, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Elisabeth Maurer (E)

European Neuroendocrine Tumor Society, Philipps University, Marburg, Germany.
Department of Visceral, Thoracic and Vascular Surgery, Philipps University, Marburg, Germany.

Birgitte Federspiel (B)

European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.
Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Peter H Kann (PH)

European Neuroendocrine Tumor Society, Philipps University, Marburg, Germany.
Department of Gastroenterology and Division of Endocrinology, Philipps University, Marburg, Germany.

Detlef K Bartsch (DK)

European Neuroendocrine Tumor Society, Philipps University, Marburg, Germany.
Department of Visceral, Thoracic and Vascular Surgery, Philipps University, Marburg, Germany.

Ulrich Knigge (U)

Department of Endocrinology Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
European Neuroendocrine Tumor Society Center of Excellence, Rigshospitalet, Copenhagen, Denmark.
Department of Surgery, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

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