Literature DB >> 3578240

Nesidioblastosis in an adult: an illustrative case and collective review.

T Carlson, M L Eckhauser, B DeBaz, A Khiyami, C H Park.   

Abstract

Nesidioblastosis is a term that describes multifocal hyperplasia of all pancreatic cell components and is characterized primarily by their disorganization and proliferation throughout the entire pancreas. This condition is the most common cause of persistent neonatal hypoglycemia. Since it is so exceedingly rare in adults no consensus regarding its surgical management is available. Our patient underwent celiotomy with a presumptive diagnosis of insulinoma. No adenoma was found and frozen sections suggested hyperplasia. Even when Whipple's triad is met and all biochemical and roentgenographic analyses suggest insulinoma, another etiology may be the cause. Intraoperative ultrasonography may aid in the diagnosis especially after a negative exploration. The diagnosis of nesidioblastosis can be confirmed by frozen section especially if adenomatosis is present. The degree of resection required is problematic because no large series exists. This case is presented with special emphasis given to etiology, pathology, preoperative work-up, and operative strategy.

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Year:  1987        PMID: 3578240

Source DB:  PubMed          Journal:  Am J Gastroenterol        ISSN: 0002-9270            Impact factor:   10.864


  3 in total

Review 1.  Adult nesidioblastosis: a case report and review of the literature.

Authors:  R D Rinker; K Friday; F Aydin; B M Jaffe; L Lambiase
Journal:  Dig Dis Sci       Date:  1998-08       Impact factor: 3.199

2.  Hyperinsulinemic hypoglycemia due to diffuse nesidioblastosis in adults: a case report.

Authors:  Ran Hong; Dong-Youl Choi; Sung-Chul Lim
Journal:  World J Gastroenterol       Date:  2008-01-07       Impact factor: 5.742

3.  Diffuse nesidioblastosis with hypoglycemia mimicking an insulinoma: a case report.

Authors:  Chiara Ferrario; Delphine Stoll; Ariane Boubaker; Maurice Matter; Pu Yan; Jardena J Puder
Journal:  J Med Case Rep       Date:  2012-10-02
  3 in total

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