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产后诊断的胰岛素瘤:临床和免疫组织化学特征。

Insulinoma diagnosed in the postpartum: clinical and immunohistochemical features.

机构信息

Ambulatory of Gonadal and Adrenal Diseases, Endocrinology Unit, University Hospital of Brasilia, Brazil.

出版信息

Gynecol Endocrinol. 2012 Aug;28(8):633-6. doi: 10.3109/09513590.2011.650756. Epub 2012 Feb 2.

DOI:10.3109/09513590.2011.650756
PMID:22296647
Abstract

Insulinomas are rare pancreatic β-cell tumors with an estimated incidence of 1:250.000 persons/year. We present a novel case of insulinoma manifesting immediately after childbirth. Eight days after delivery, a 21-year-old, previously healthy woman presented paresthesia in hands, upper and lower limbs muscle weakness with difficult walking, which worsened during breastfeeding sessions. Laboratory tests showed blood glucose levels between 37 and 55 mg/dL with inappropriately normal insulin levels (7.78 μUI/mL; normal range: 5-29). An abdominal computed tomography showed a nodular lesion measuring 2 cm at the head of the pancreas. Tumor enucleation resulted in complete resolution of hypoglycemia. Histopathological and immunohistochemical analysis were consistent with an insulinoma. About 27 cases of insulinoma associated with pregnancy have been reported to date, mostly diagnosed before the 16th week. The beginning of symptoms soon after delivery is less common. Understanding the interactions between pancreatic β-cell function and all the physiological metabolic and hormonal adaptations associated with gestation is essential for the adequate management of hypoglycemic disorders in pregnant women.

摘要

胰岛素瘤是一种罕见的胰腺β细胞肿瘤,估计发病率为 1:250000 人/年。我们报告了一例新的胰岛素瘤病例,该病例在分娩后立即出现。一位 21 岁、既往健康的女性在分娩后 8 天出现手部感觉异常、上下肢肌无力,行走困难,在哺乳过程中症状加重。实验室检查显示血糖水平在 37 至 55mg/dL 之间,而胰岛素水平(7.78μUI/mL;正常范围:5-29)不适当正常。腹部 CT 显示胰腺头部有一个 2cm 的结节性病变。肿瘤切除术导致低血糖完全缓解。组织病理学和免疫组织化学分析与胰岛素瘤一致。迄今为止,已有约 27 例与妊娠相关的胰岛素瘤病例被报道,其中大多数在第 16 周前被诊断。分娩后不久开始出现症状的情况较少见。了解胰腺β细胞功能与妊娠相关的所有生理代谢和激素适应之间的相互作用对于孕妇低血糖症的适当管理至关重要。

相似文献

1
Insulinoma diagnosed in the postpartum: clinical and immunohistochemical features.产后诊断的胰岛素瘤:临床和免疫组织化学特征。
Gynecol Endocrinol. 2012 Aug;28(8):633-6. doi: 10.3109/09513590.2011.650756. Epub 2012 Feb 2.
2
Insulinoma in a third-trimester pregnant woman combined with pre-eclampsia: a case report and review of the diagnostic strategies.孕晚期孕妇胰岛素瘤合并子痫前期:一例病例报告及诊断策略综述
Gynecol Endocrinol. 2008 Jul;24(7):417-22. doi: 10.1080/09513590802210931.
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Insulinoma in pregnancy.妊娠期胰岛素瘤
Exp Clin Endocrinol Diabetes. 2010 Jan;118(1):9-18. doi: 10.1055/s-0029-1202272. Epub 2009 Apr 16.
4
[Detection of an insulinoma in pregnancy--a rare cause of hypoglycemia].[妊娠期胰岛素瘤的检测——低血糖的罕见病因]
Wien Klin Wochenschr. 1994;106(13):426-9.
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Insulinoma complicating pregnancy presenting with hypoglycemic coma after delivery: a case report and review of the literature.胰岛素瘤合并妊娠产后出现低血糖昏迷:一例病例报告及文献复习
Obstet Gynecol. 1989 May;73(5 Pt 2):847-9.
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Insulinoma associated with pregnancy.胰岛素瘤与妊娠相关。
Fertil Steril. 2008 Jul;90(1):199.e1-4. doi: 10.1016/j.fertnstert.2007.06.092. Epub 2007 Nov 5.
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[Insulinoma and pregnancy. A clinical case].[胰岛素瘤与妊娠。一例临床病例]
Rev Chil Obstet Ginecol. 1992;57(6):437-9.
8
Insulinoma in pregnancy: a case report and review of the literature.妊娠期胰岛素瘤:一例病例报告及文献复习
Obstet Gynecol Surv. 2002 Apr;57(4):229-35. doi: 10.1097/00006254-200204000-00022.
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Sporadic insulinoma in a 10-year-old boy: a case report and literature review.一名10岁男孩的散发性胰岛素瘤:病例报告及文献综述
JOP. 2014 Jan 10;15(1):53-7. doi: 10.6092/1590-8577/1925.
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[Insulinoma associated with pregnancy].[妊娠相关胰岛素瘤]
Dtsch Med Wochenschr. 2010 Jul;135(30):1484-6. doi: 10.1055/s-0030-1262436. Epub 2010 Jul 20.

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A case of insulinoma diagnosed postpartum with hypoglycemic symptoms that were masked during pregnancy.一例产后诊断的胰岛素瘤,其低血糖症状在孕期被掩盖。
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Insulinoma in pregnancy (a case presentation and systematic review of the literature).妊娠期胰岛素瘤(病例报告及文献系统综述)
Rare Tumors. 2021 Feb 7;13:2036361320986647. doi: 10.1177/2036361320986647. eCollection 2021.
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Hypoglycemia identified by a continuous glucose monitoring system in a second-trimester pregnant woman with insulinoma: a case report.胰岛素瘤致孕中期孕妇连续血糖监测系统识别低血糖:一例报告
J Med Case Rep. 2017 Apr 21;11(1):117. doi: 10.1186/s13256-017-1265-8.