Literature DB >> 11961480

Insulinoma in pregnancy: a case report and review of the literature.

Catherine A Takacs1, Thomas C Krivak, Peter G Napolitano.   

Abstract

UNLABELLED: Insulinomas are rare tumors with an incidence of approximately four cases per million person-years. Nineteen cases of insulinoma during pregnancy have been reported. Hypoglycemic symptoms usually appear during the first trimester. A 28-year-old primigravida was admitted at 6 weeks of gestation after referral for uncontrolled seizures. Her previous seizure work-up included a normal EEG and a normal magnetic resonance imaging of the brain. Elevated fasting insulin and C-peptide levels accompanied severe hypoglycemia. The patient was managed with glucose monitoring, frequent small meals, and rare doses of glucagon. Postpartum testing was consistent with insulinoma, and magnetic resonance imaging indicated a mass in the tail of the pancreas. During surgical exploration with intraoperative ultrasound, two insulinomas were removed from the tail of the pancreas. The hypoglycemic episodes resolved and the fasting glucose levels normalized. Insulinomas are rare in pregnancy and can be difficult to diagnose. Symptoms may resolve during the second and third trimesters, possibly due to changes in glucose metabolism associated with pregnancy. Misdiagnosis has been fatal. Careful management during pregnancy and aggressive treatment after delivery are essential. TARGET AUDIENCE: Obstetricians and Gynecologists, Family Physicians. LEARNING
OBJECTIVES: After completion of this article, the reader will be able to describe the pathophysiology of an insulinoma, to list the potential tests used to make the diagnosis of insulinoma, and to outline potential treatment options for a patient with an insulinoma.

Entities:  

Mesh:

Year:  2002        PMID: 11961480     DOI: 10.1097/00006254-200204000-00022

Source DB:  PubMed          Journal:  Obstet Gynecol Surv        ISSN: 0029-7828            Impact factor:   2.347


  4 in total

1.  Non-functioning, malignant pancreatic neuroendocrine tumour (PNET): a rare entity during pregnancy.

Authors:  Carsten H Kamphues; Christoph Röcken; Peter Neuhaus; Ulf P Neumann
Journal:  Langenbecks Arch Surg       Date:  2008-05-30       Impact factor: 3.445

2.  A case of insulinoma diagnosed postpartum with hypoglycemic symptoms that were masked during pregnancy.

Authors:  Tomoe Abe; Yasutaka Takeda; Takao Takiyama; Ayaka Sasaki; Ryoichi Bessho; Mao Sato; Hiroya Kitsunai; Hidemitsu Sakagami; Atsuko Abiko; Koji Imai; Sayaka Yuzawa; Mishie Tanino; Yumi Takiyama
Journal:  Clin Case Rep       Date:  2021-02-16

3.  Functioning Endocrine Tumors in Pregnancy: Diagnostic and Therapeutic Challenges.

Authors:  Kripa E Cherian; Nitin Kapoor; Thomas V Paul; Hesarghatta S Asha
Journal:  Indian J Endocrinol Metab       Date:  2021-12-15

4.  Pancreatic neuroendocrine carcinoma in a pregnant woman: A case report and review of the literature.

Authors:  Li-Ping Gao; Gui-Xiang Kong; Xiang Wang; Hui-Min Ma; Fei-Fei Ding; Ting-Dong Li
Journal:  World J Clin Cases       Date:  2021-06-16       Impact factor: 1.337

  4 in total

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