Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Abstract
Abstracts
Author Reply
Author's Reply
Book Review
Brief Communication
Case Report
Case Series
Commentary
Continuing Medical Education
Diagnosis
Down the Memory Lane
Editorial
Erratum
Faculty
Free papers: Oral Session
Free papers: Poster Session
From Editor's desk
From The Chair, Scientific Committee
Guest Editorial
Image Challenge
In Memoriam
Interesting Image
Interesting Images
Invited Review
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Message
Message by President Elect, SNM, India
Message by President, SNM, India
Messages
Obituary
Oral
ORAL PRESENTATION
Original Article
Pictorial Essay
Pictorial Teaching Essay
POSTER PRESENTATION
President's Message
Presidents’ Wall of Fame
Review
Review Article
Schedule for Paper Presentations
Scientific Program
Secretary's Message
Short Communication
SNM India Guidelines 1.0
Technical Communication
Technical Note
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Abstract
Abstracts
Author Reply
Author's Reply
Book Review
Brief Communication
Case Report
Case Series
Commentary
Continuing Medical Education
Diagnosis
Down the Memory Lane
Editorial
Erratum
Faculty
Free papers: Oral Session
Free papers: Poster Session
From Editor's desk
From The Chair, Scientific Committee
Guest Editorial
Image Challenge
In Memoriam
Interesting Image
Interesting Images
Invited Review
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Message
Message by President Elect, SNM, India
Message by President, SNM, India
Messages
Obituary
Oral
ORAL PRESENTATION
Original Article
Pictorial Essay
Pictorial Teaching Essay
POSTER PRESENTATION
President's Message
Presidents’ Wall of Fame
Review
Review Article
Schedule for Paper Presentations
Scientific Program
Secretary's Message
Short Communication
SNM India Guidelines 1.0
Technical Communication
Technical Note
View/Download PDF

Translate this page into:

Case Report
28 (
3
); 163-164
doi:
10.4103/0972-3919.119547

Diffuse nesidioblastosis diagnosed on a Ga-68 DOTATATE positron emission tomography/computerized tomography

Department of Nuclear Medicine and PET, Post Graduate Institute of Medical Education and Research, Chandigarh, India
Department of Paediatrics, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Address for correspondence: Dr. Bhagwant Rai Mittal, Department of Nuclear Medicine and PET, Post Graduate Institute of Medical Education and Research, Chandigarh - 160 012, India. E-mail: brmittal@yahoo.com

Licence

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Disclaimer:
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.

Abstract

The authors describe a 50 days old pre-term infant with persistent hyperinsulinemic hypoglycemia of infancy in whom Ga-68 DOTATATE positron emission tomography/computerized tomography scan showed diffusely increased tracer uptake in the entire pancreas with no abnormal tracer uptake anywhere else in the body, suggestive of a diffuse variant of nesidioblastosis.

Keywords

Ga-68 DOTATATE
hyperinsulinemic hypoglycaemia
infant
nesidioblastosis
positron emission tomography/computerized tomography

INTRODUCTION

Nesidioblastosis is a pathological condition caused by neo-differentiation of islets of Langerhans from pancreatic ductal epithelium. This condition later renamed as persistent hyperinsulinemic hypoglycaemia of infancy (PHHI) exists in two forms. One corresponds to a focal pancreatic adenomatous hyperplasia (focal PHHI) and the other is characterized by a diffuse cell abnormality (diffuse PHHI). The underlying pathology and treatment strategies are different for both the types however differentiation by clinical and biochemical parameters is not feasible. No definite role of imaging to differentiate diffuse versus focal condition has been reported in the literature.

CASE REPORT

A 50-day-old pre-term female infant presented with persistent hyperinsulinemic hypoglycemia. The child was born at 35 weeks of gestation, with breathing difficulty since birth. She developed cyanosis on day 2 of life with seizures thereafter. On investigation the child was found to be hypoglycemia (blood glucose level = 16.8 mg/dl) and hyperinsulinemia with serum insulin levels of 149.70 IU/ml (n = 2.0 IU/ml). Screening for sepsis was negative. The child required intravenous glucose infusion up to 10 mg/kg/min and oral feeds fortified with glucose to maintain euglycemic state. Ga-68 DOTATATE positron emission tomography/computerized tomography (PET/CT) scan showed diffusely increased tracer uptake in the entire pancreas with no abnormal tracer uptake anywhere else in the body, suggestive of a diffuse variant of nesidioblastosis [Figure 1]. The child is currently on injection octreotide but not fit for definitive surgical management (near total pancreatectomy).

Ga-68 DOTATATE positron emission tomography/computed tomography (CT) (a) Maximum intensity projection (b) transaxial CT (c) transaxial fused images showing diffusely increased tracer uptake in the entire pancreas (arrow) with no abnormal tracer uptake elsewhere in the body, suggestive of a diffuse variant of nesidioblastosis
Figure 1 Ga-68 DOTATATE positron emission tomography/computed tomography (CT) (a) Maximum intensity projection (b) transaxial CT (c) transaxial fused images showing diffusely increased tracer uptake in the entire pancreas (arrow) with no abnormal tracer uptake elsewhere in the body, suggestive of a diffuse variant of nesidioblastosis

DISCUSSION

Laidlaw in 1938 first identified the disease and coined the term nesidioblastosis to describe the neodifferentiation of islets of Langerhans from pancreatic ductal epithelium.[1] This condition later renamed as PHHI of infancy exists in two forms. One corresponds to a focal pancreatic adenomatous hyperplasia (focal PHHI) and the other is characterized by a diffuse cell abnormality (diffuse PHHI).[234] These two forms could not be differentiated by clinical or biochemical data, although their underlying pathological mechanisms and the treatment remains totally different.[5] F18-fluoro-dihydroxyphenylalanine (F-DOPA) PET scan has been used to detect the hyperfunctional pancreatic islet tissue and to differentiate between focal and diffuse PHHI with a reported accuracy of 96% in diagnosing focal or diffuse disease and 100% in localizing the focal lesion.[67] The principle behind the use of F-DOPA PET in PHHI is that neuroendocrine pancreatic cells have an affinity for taking up F-DOPA and decarboxylate it into dopamine through aromatic amino acid decarboxylase.[8] Similarly neuroendocrine cells of pancreas also express high affinity somatostatin receptors (SSTR). 68-Ga DOTATATE specifically binds to the SSTR type II, which are highly concentrated in the pancreatic islet cells.[9] Previously only one case report was published where Ga-68 DOTATOC PET scan was used to differentiate focal versus diffuse nesidioblastosis with limited success.[10] This is the first case where Ga-68 DOTATATE PET scan had been used to successfully differentiate focal versus diffuse nesidioblastosis and thus help in tailoring the management in the infant.

Source of Support: Nil.

Conflict of Interest: None declared.

REFERENCES

  1. , . Nesidioblastoma, the islet tumor of the pancreas. Am J Pathol. 1938;14:125-134. 5
    [Google Scholar]
  2. , , , , , , . Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: The pathologist's role. Histopathology. 1998;32:15-9.
    [Google Scholar]
  3. , , , , , , . Neonatal hyperinsulinemic hypoglycemia: Heterogeneity of the syndrome and keys for differential diagnosis. J Clin Endocrinol Metab. 1998;83:1455-61.
    [Google Scholar]
  4. , , , , , , . Clinical features of 52 neonates with hyperinsulinism. N Engl J Med. 1999;340:1169-75.
    [Google Scholar]
  5. , , , . Persistent hyperinsulinaemic hypoglycaemia of infancy: A heterogeneous syndrome unrelated to nesidioblastosis. Arch Dis Child Fetal Neonatal Ed. 2000;82:F108-12.
    [Google Scholar]
  6. , , , , , , . Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-DOPA. J Nucl Med. 2005;46:560-6.
    [Google Scholar]
  7. , , , , , , . Diagnosis and localization of focal congenital hyperinsulinism by 18F-fluorodopa PET scan. J Pediatr. 2007;150:140-5.
    [Google Scholar]
  8. , , , . Cell biology, clinicopathological profile, and classification of gastro-enteropancreatic endocrine tumors. J Mol Med (Berl). 1998;76:413-20.
    [Google Scholar]
  9. , , , . Nuclear imaging of neuroendocrine tumors. Best Pract Res Clin Endocrinol Metab. 2007;21:69-85.
    [Google Scholar]
  10. , , , , , , . Novel use of somatostatin receptor scintigraphy in localization of focal congenital hyperinsulinism: Promising but fallible. J Pediatr Endocrinol Metab. 2009;22:965-9.
    [Google Scholar]

Fulltext Views
32

PDF downloads
16
View/Download PDF
Download Citations
BibTeX
RIS
Show Sections