E-Poster Presentation 63rd Endocrine Society of Australia Annual Scientific Meeting 2020

Agenesis of the dorsal pancreas: a rare incidental finding which is amongst the differential diagnoses for abdominal pain and diabetes mellitus. (#129)

Varun Manoharan 1 2 3 , Minoli V Abeysekera 1 2 4 , Emily Hibbert 1 2
  1. Department of Endocrinology, Nepean Hospital, Penrith, NSW, Australia
  2. Nepean Clinical School , Faculty of Medicine and Health, The University of Sydney, NSW
  3. South Western Sydney Clinical School, University of New South Wales, Sydney, NSW
  4. Griffith Medical School, Griffith University, Gold Coast, Queensland

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INTRODUCTION

In parallel with improvement in imaging technologies, there has been an increase in the frequency of incidental diagnosis of agenesis of the dorsal pancreas. Yet this congenital malformation remains rare; its manifestations include diabetes mellitus, abdominal pain and pancreatitis1. We report a case of a 39 year old man with antibody-negative type 1 diabetes and abdominal pain, who was incidentally found to have dorsal agenesis of the pancreas on abdominal CT performed to investigate his chronic abdominal pain.

 

CASE SUMMARY

A 39 year old Caucasian man from non-consanguineous kinships presented to the Diabetes Service in 2020 for ongoing management of his type 1 diabetes mellitus. He reported longstanding colicky epigastric pain associated with intermittent diarrhoea without any blood or mucus in his stools. His abdominal pain was exacerbated by fatty meals. He reported significant loss of appetite but denied any extraintestinal symptoms suggestive of inflammatory bowel disease. His drug and alcohol history was unremarkable.

He was diagnosed with antibody negative type 1 diabetes mellitus three years prior, when he presented with polyuria, polydipsia and unintentional weight loss. Further investigations performed at diagnosis showed a relative insulin deficiency with a C-peptide level of 1.0 ug/L [0.8-3.4], fasting serum insulin level of 6 mu/l [<10] with a paired random plasma glucose level of 27.1 mmol/L and HbA1c of 9.6% (Table 1). Autoantibodies for Glutamic Acid Decarboxylase, Islet cell, Insulin and Zinc transporter 8 were not detected. However, he had other features of automimmunity. He was subclinically hypothyroid (Table 1) with elevated thyroid peroxidase antibody >1300 U/mL [<60]. His coeliac serology was negative and he had a vitamin B12 level of 205pmol/L [150pmol/L]. A diagnosis of Hashimoto’s thyroiditis and failure to achieve good glycaemic control on oral hypoglycaemic agents led to a diagnosis of antibody negative type 1 diabetes mellitus. Notably, there was no history of diabetic ketoacidosis or evidence of diabetes complications.

His background history was significant for dyslipidaemia, gastroesophageal reflux disease and a family history of autoimmune thyroid disease. Regular medications included basal-bolus insulin therapy, thyroxine, atorvastatin, pantoprazole and panadeine forte for his colicky abdominal pain.

On examination, he weighed 79 kilograms and had a body mass index of 25.5kg/m2. Cardiorespiratory and gastrointestinal examinations were unremarkable.

Laboratory investigations in 2020 showed an HbA1c of 8.6%. He was replete for micronutrients and fat soluble vitamins, and was biochemically euthyroid. His full blood count, pancreatic enzymes and renal function were all within normal limits (Table 2). Repeat C-peptide level was low 0.68 ug/L [0.8-3.4] with a paired blood glucose level of 11.4 mmol/L. Agenesis of the dorsal pancreas was noted on CT imaging of the abdomen demonstrated agenesis of the dorsal pancreas. There were no focal pancreatic lesions or evidence of acute or chronic pancreatitis. This was confirmed on MRCP which also showed normal hepatobiliary anatomy (Figure 1). His faecal elastase was 317 microg/g [>100 microg/g].

His abdominal pain improved with cessation of panadeine forte and good glycaemic control was achieved with up titration of his insulin therapy.

 

DISCUSSION

ADP is a rare congenital abnormality that arises from dysgenesis of the dorsal pancreatic bud. The dorsal endodermal bud forms the upper part of the head, body and tail of the pancreas, whilst the ventral bud develops into the posterior part of the pancreatic head, uncinate process and main pancreatic duct of the pancreas2. Strict signalling pathways regulate the fusion of the ventral and dorsal buds and subsequent morphogenesis and differentiation of multipotent progenitor cells into acinar, ductal and endocrine cells. The acinar and ductal cells comprise 99% of the pancreatic mass and fulfil the exocrine functions, whilst the Islet cells of Langerhans comprise the remainder of pancreatic tissue. Associations between embryogenesis of the pancreas and genes such as HNF1B3 and GATA64, and signalling pathways such as retinaldehyde dehydrogenase 2 (Raldh2)5 have been reported in the literature. Yet this condition remains rare with less than one hundred and twenty cases reported in the literature6-9.

Most patients with ADP remain asymptomatic; it is often identified incidentally on abdominal imaging. However, if symptomatic, abdominal pain is the commonest symptom at presentation1. Abdominal pain among patients with ADP has been postulated to be due to pancreatitis, duodenal obstruction and sphincter of Oddi dysfunction6. Our patient had normal amylase and lipase levels and there were no features suggestive of acute or chronic pancreatitis on abdominal imaging. We noted that he was on panadeine forte for abdominal pain, and cessation of panadeine forte and commencement of paracetamol for abdominal pain resulted in improvement in abdominal pain. Panadeine forte contains codeine, which has been shown to increase the basal pressure of the sphincter of Oddivia the non mu opioid receptor and results in spasm of the sphincter of Oddi.

Patients with ADP can present with symptoms of endocrine and exocrine deficiency. Approximately half of patients with ADP will develop diabetes mellitus, and up to half of them will require insulin therapy7-9. The age of onset of diabetes mellitus associated with ADP ranges between 28 to 39 years7-9. Although beta cell dysfunction and insulin deficiency have been implicated in the pathophysiology of diabetes mellitus among patients with ADP, there have only been three studies that reported a correlation between this congenital malformation and diabetic ketoacidosis7,9. Studies conducted on patients who have undergone surgical resection of the pancreas for other indications demonstrate that the pancreatic tail in humans is more densely populated with Islets of Langerhans than other parts of the pancreas. Animal studies have shown functional differences in these islets based on their location, whereby islets originating from the dorsal pancreatic bud have greater capacity to secrete and synthesise insulin than islets of ventral bud origins10. These studies have shown that removal of the pancreatic tail led to elevated fasting glucose and post-challenge hyperglycaemia, whilst removal of the pancreatic head caused an improvement in oral glucose tolerance. Very few cases of ADP reported in the literature have paired C-peptide levels measured. Our patient had a low-normal C-peptide level of 1.0 ug/L [0.8-3.4] and serum insulin level of 7 mu/l [<10] with a paired random blood glucose level 27.1 mmol/L around the time of diagnosis, highlighting how variable degrees of β-cell dysfunction contribute to dysglycaemia among patients with agenesis of the dorsal pancreas.

Steatorrhoea is a manifestation of exocrine deficiency and is commonly managed with supplementation of pancreatic enzymes. ADP has been associated with include polysplenia, ectopic spleen, bowel malrotation, horseshoe kidney, congenital heart disease and heterotaxy7, none of which were noted on our patient’s CT abdomen and MRCP.

There has been an increased frequency of incidental diagnosis of ADP6,7. Abdominal CT assists in the diagnosis of ADP, and MRCP helps characterise the anatomy of the biliary ductal system6.

CONCLUSION

In summary, ADP is an extremely rare condition that is often asymptomatic but can also present with abdominal pain or with features of exocrine and endocrine deficiency. It is often diagnosed incidentally on abdominal imaging.

TAKE HOME MESSAGES

  • Agenesis of dorsal pancreas is a rare clinical entity
  • Abdominal pain is the commonest symptom at presentation, but it is often entirely asymptomatic
  • It is usually diagnosed incidentally on imaging
  • Patients can present with features of exocrine or endocrine deficiency
  • Agenesis of dorsal pancreas is associated with other congenital abnormalities
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