Focal form of congenital hyperinsulinism clearly detectable by contrast-enhanced computed tomography imaging
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The focal form of congenital hyperinsulinism (CHI) is characterized by a cluster of abnormal insulin-oversecreting β cells within a restricted area of the pancreas. Although identification of the focal lesion is very important in the management of CHI, it has been reported that imaging studies, including computed tomography (CT), magnetic resonance imaging (MRI) scans, or angiography, are not helpful in identifying the focal lesion. Currently, fluorine-18-L-dihydroxyphenylalanine positron emission tomography (18F-DOPA PET) is believed to be the only imaging modality that can identify the focal lesions. In this report, however, we present a case of a 7-month-old girl with the focal form of CHI, caused by a loss-of-function mutation in the ABCC8 gene, whose lesion was clearly visible as a hyperenhancing nodule on contrast-enhanced CT and dynamic MRI imaging.
KeywordsKATP Channel Focal Lesion Focal Form ABCC8 Gene Hyperinsulinemic Hypoglycemia
Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycemia in the neonatal/infantile period which often requires pancreatectomy when unresponsive to medical treatments [1, 2, 3, 4, 5, 6, 7].
There are two known histological forms of CHI: diffuse and focal. The focal form is characterized by a cluster of abnormal insulin-oversecreting β cells within a restricted area of the pancreas, whereas in the diffuse form, abnormal β cells are scattered throughout the pancreas. Focal CHI arises in individuals with a paternally inherited monoallelic mutation in one of the genes coding for pancreatic ATP-sensitive potassium channel (KATP channel), KCNJ11 or ABCC8, both located side-by-side in the chromosomal 11p15.1 region [8, 9]. When a second event of paternal uniparental disomy at chromosome 11p15 occurs in a β cell during the development of the pancreas, that particular cell loses the KATP channel activity, and also loses the activity of H19 and CDKN1C, which are adjacent imprinted tumor suppressor genes, expressed only from the maternal allele. Moreover, in 11p15.5, there is an oppositely imprinted growth factor gene, IGF2, which is expressed only from the paternal allele. The gene dosage of IGF2 would be doubled when paternal uniparental disomy takes place. Consequently, the insulin-oversecreting abnormal β cell acquires a growth advantage, eventually forming a focus of abnormal β cells [10, 11, 12].
Since the focal form of CHI can be cured by partial pancreatectomy without postsurgical diabetes mellitus, when a patient is unresponsive to conservative therapy, identification of the focal lesion is very important. It has been reported that imaging studies, including computed tomography (CT), magnetic resonance imaging (MRI) scans, or angiography, are not helpful in identifying focal lesions, since they do not distort the surrounding normal pancreatic structure, and also lack significant vascularization [13, 14]. Localization of the focal form, therefore, has been identified only by fluorine-18-L-dihydroxyphenylalanine positron emission tomography (18F-DOPA PET) scans or by invasive diagnostic procedures such as arterial stimulation with venous sampling (ASVS) or transhepatic portal venous sampling (THPVS) [15, 16, 17].
In this report, however, we present a case of a 7-month-old girl with the focal form of KATP channel CHI whose lesion was clearly visible as a hyperenhancing nodule on contrast-enhanced CT and dynamic MRI imaging corresponding to the site detected by 18F-DOPA PET scan.
The patient was a 7-month-old Japanese girl who was born after 39 weeks of an uneventful pregnancy, with a birth weight of 3792 g (+2.4 standard deviation [SD]) and length 54 cm (+2.7 SD). Both parents were healthy and there was no family history of hypo- or hyperglycemia. On the second day of life, she presented with hypothermia associated with hypoglycemia. A diagnosis of hyperinsulinemic hypoglycemia was made, based on the characteristic findings at the time of hypoglycemia: plasma glucose 1.6 mmol/L with serum insulin 26.7 pmol/L, undetectable ketone bodies, normal lactate, and normal ammonia. She was unresponsive to diazoxide at a dose of 20 mg/kg/day, and required 8.6 mg/kg/min of intravenous glucose infusion to maintain normoglycemia. From the 15th day of life, continuous subcutaneous octreotide infusion was started, and at 25 μg/kg/day of octreotide, glucose infusion could be stopped. However, hypoglycemic episodes persisted quite often despite frequent feedings. Fortunately, her psychosocial growth and psychomotor development remained within the normal range despite frequent hypoglycemic episodes.
Mutational analysis was performed as described previously . Briefly, all exons and exon-intron boundaries of the KATP channel genes were amplified from genomic DNA and directly sequenced. Laser microdissection was performed using the Arcturus PIXCELL IIe (Life Technologies, Carlsbad, CA) instrument, as described in the manufacturer instructions. The study protocol was approved by the Institutional Review Board (No. 743), and written informed consent was obtained from the guardians of the patient.
Contrary to the previous belief, our report shows that some of the focal KATP-channel CHI can be visualized by conventional imaging modalities such as contrast-enhanced CT or dynamic MRI imaging. Although CT scans are not advisable for infants in view of the risk of irradiation, MRI imaging might be worth trying especially where 18F-DOPA PET scans are not easily available.
The reason why the focal lesion of our patient could be clearly visualized by contrast-enhanced CT and MRI scans is not clear. Generally, for pancreatic nodules to be visualized by these imaging modalities, they need to grow fast enough to have a mass effect. In addition, they need to have a higher vascularity, or higher vascular permeability, to be enhanced by the contrast media. The focal lesion of our patient somehow attained both of these properties. In contrast, the size and cell density of the lesion do not appear to be critical factors for visualization by these techniques [19, 20].
Since the tumor suppressor activity of our patient is presumed to be lost as in all other cases of focal CHI, the higher growth potential of the focal lesion in this case might be explained by a difference in the growth promoting activity of the IGF2 gene, although no mutations could be identified in the coding region of IGF2 in our patient (data not shown).
Microscopically, the vascularity in the focal lesion of our patient was not particularly different from that of other patients with the focal form of CHI. However, if the focal lesion has higher growth potential, capillary dilatation without angiogenesis could follow , which might explain the contrast enhancement observed in our patient.
We report the unprecedented findings in a case of a focal form of CHI whose lesion was clearly visible as a hyperenhancing nodule on contrast-enhanced CT and dynamic MRI imaging. The mechanism leading to the visualization of the focal lesion in our patient needs further investigation.
Written informed consent was obtained from the parents of the patient for publication of this Case Report and the accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
We thank the parents of the patient for participating in the study. This work was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan to TY (No. 15K09636).
- 17.de Lonlay P, Simon-Carre A, Ribeiro MJ, Boddaert N, Giurgea I, Laborde K, et al. Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion. J Clin Endocrinol Metab. 2006;91:933–40.CrossRefPubMedGoogle Scholar
- 18.Yorifuji T, Kawakita R, Nagai S, Sugimine A, Doi H, Nomura A, et al. Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes. J Clin Endocrinol Metab. 2011;96:E141–5.CrossRefPubMedGoogle Scholar
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