Literature DB >> 22430908

Surgical management of insulinomas: short- and long-term outcomes after enucleations and pancreatic resections.

Stefano Crippa1, Alessandro Zerbi, Letizia Boninsegna, Vanessa Capitanio, Stefano Partelli, Gianpaolo Balzano, Paolo Pederzoli, Valerio Di Carlo, Massimo Falconi.   

Abstract

OBJECTIVE: To analyze the characteristics and outcomes following enucleation and pancreatic resections of insulinomas.
DESIGN: Retrospective cohort study; prospective database. SETTINGS: Academic, tertiary, and referral centers. PATIENTS: Consecutive patients with insulinomas (symptoms of hyperinsulinism and positive fasting glucose test) who underwent surgical treatment between January 1990 and December 2009. MAIN OUTCOME MEASURES: Operative morbidity, tumor recurrence, and survival after treatment.
RESULTS: A total of 198 patients (58.5% women; median age, 48 years) were identified. There were 175 (88%) neuroendocrine tumors grade G1 and 23 (12%) neuroendocrine tumors grade G2. Malignant insulinomas defined by lymph node/liver metastases were found in 7 patients (3.5%). Multiple insulinomas were found in 8% of patients, and 5.5% of patients had multiple endocrine neoplasia type 1. Surgical procedures included 106 enucleations (54%) and 92 pancreatic resections (46%). Mortality was nil. Rate of clinically significant pancreatic fistula was 18%. Enucleations had a higher reoperation rate compared with pancreatic resections (8.5% vs 1%; P = .02). Multiple endocrine neoplasia type 1 was significantly associated with younger age at onset (P < .005) and higher rates of malignancies and multiple lesions. Median follow-up was 65 months. Six patients (3%; 5 patients had neuroendocrine tumors grade G2) developed tumor recurrence. Four patients (2%) died of disease. New exocrine (1.5%) and endocrine (4%) insufficiencies were associated only with pancreatic resections.
CONCLUSIONS: Outcomes following surgical resection of insulinomas are satisfactory, with no mortality and good functional results. Recurrence is uncommon (3%), and it is more likely associated with neuroendocrine tumors grade G2. Insulinomas in multiple endocrine neoplasia type 1 are at higher risk for being malignant and multifocal, requiring pancreatic resections.

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Mesh:

Year:  2012        PMID: 22430908     DOI: 10.1001/archsurg.2011.1843

Source DB:  PubMed          Journal:  Arch Surg        ISSN: 0004-0010


  38 in total

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2.  Open and minimally invasive pancreatic neoplasms enucleation: a systematic review.

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4.  Clinical characteristics and incidence of glucose metabolism disorders during the follow-up of surgically treated insulinomas.

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Review 5.  Systematic Review and Metaanalysis of Lymph Node Metastases of Resected Pancreatic Neuroendocrine Tumors.

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6.  The surgical management of insulinomas in children.

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7.  Sporadic Insulinoma Presenting as Early Morning Night Terrors.

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Review 8.  The treatment of hyperinsulinemic hypoglycaemia in adults: an update.

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9.  Re-occurrence of pancreatic insulinoma: an usual cause of hypoglycaemia.

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Review 10.  Place of surgical resection in the treatment strategy of gastrointestinal neuroendocrine tumors.

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