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PERTRIGLYCERIDEMIA INDUCED PANCREATITIS
Case Report 
Department of Gastroenterology, Apollo Hospitals, Greams Road, Chennai 600 006, India. 
Correspondence: Dr K R Palaniswamy, Senior Consultant, Department of Gastroenterology, Apollo Hospitals, 
Background: A 32 year-old female presented to the emergency department complaining of 12 hours upper 
abdominal pain accompanied by 2-3 episodes of vomiting.Case report: The patient had a heavy meal a few 
hours before. There were no signs of peritonitis. Routine laboratory examinations revealed leukocytosis, 
hyperglycemia and hyperamylasemia (serum amylase: 336 mg/dL).Conclusion:The lipid profile revealed an 
impressive elevation of triglycerides (4240 mg/dL). The serum was extremely lipemic. The abdomen 
computed tomography confirmed the diagnosis of pancreatitis. 
CASE REPORT 
HYPERTRIGLYCERIDEMIA INDUCED PANCREATITIS 
Bhavesh Thakkar, V Seshadri and KR Palaniswamy 
Greams Road, Chennai 600 006, India. 
A 32 year-old female presented to the emergency 
department complaining of 12 hour upper abdominal pain 
accompanied by 2-3 episodes of vomiting. She was a 
known diabetic for 4 years and had 2 episodes of 
pancreatitis in past. She was on oral hypoglycaemic agents 
and statins for the same. She had no history of gallstone 
disease or alcohol intake. The patient’s physical 
examination revealed a mild upper abdominal tenderness. 
There were no signs of peritonitis. The rest of the clinical 
examination was normal. Her vital signs were: Blood 
Pressure: 120/80 mmHg, Heart rate: 86 bpm. Respiratory 
Rate: 26 breaths/min, Temperature: 99ºF, Pulse Oximetry: 
95% (on air). Routine laboratory examinations revealed 
leukocytosis (WBC: 13,3 K/μL), hyperglycemia (378 mg/ 
dL) and hyperamylasemia (serum amylase: 336 mg/dL). 
BMI was 33.75 kgr/m2. The lipid profile revealed an 
impressive elevation of triglycerides (4240 mg/dL) and 
cholesterol (325 mg/dL) levels. The serum was extremely 
lipemic (Fig 1). The abdomen computed tomography 
confirmed the diagnosis of pancreatitis. The patient was 
admitted for further evaluation and treat-ment.She was 
managed conservatively with iv hydration and dietary 
restriction. Moreover, she was admitted to the ICU for 3 
days as she developed severe acidosis and respiratory 
compromise. The patient was treated with rapid acting 
insulin for 2 days during admission and underwent two 
sessions of plasmapheresis, in order to achieve quick 
improvement of triglyceride levels. She was restarted on 
lipid-lowering medications (atorvastatin, fenofibrate). Her 
clinical condition improved significantly with NIV and 
plasmapheresis and the patient was discharged in good 
health 15 days later, with a triglyceride level of 324 mg/dL. 
Uncontrolled diabetes with hypertriglyceridemia was 
probably the cause of this episode of acute pancreatitis. 
Hypertriglyceridemia is a relatively uncommon cause 
of pancreatitis [1]. Pancreatitis secondary to 
hypertriglyceri-demia typically presents as an episode of 
acute pancreatitis (AP) or recurrent pancreatitis and rarely 
as chronic pancreatitis [1,2]. An important and usually 
identifiable risk factor is a serum triglycerides level of 
1000-2000 mg/dL in a patient with an already known type 
I, IV or V hyperlipidemia (Fredrickson’s classification). 
The typical clinical profile is a patient presenting with a 
preexisting lipid abnormality in combination with a 
secondary co-releasing factor, such as poorly controlled 
Fig 1 Lipemic serum- picture after plasmapheresis. 
313 Apollo Medicine, Vol. 7, No. 4, December 2010
Case Report 
diabetes mellitus, medications related to induction of AP or 
alcohol consumption. In addition to the usual findings in 
AP, in Hyperlipidemic Pancreatitis (HLP), the serum 
pancreatic enzymes may be normal or slightly elevated [3], 
even in the presence of severe AP that has been confirmed 
by imaging techniques [2,4]. The diagnostic hallmark 
consists of a mildly elevated amylase with interestingly low 
urine amylase levels along with the presence of lipemic 
serum in a patient with a family history of disturbed lipid 
profile [1]. As far as it concerns the clinical course of HLP, 
it does resemble to that of AP derived from other causes, 
with similar complications but not in a higher rate than in 
other types of AP. Routine management should not differ 
much, aiming at a reduction of triglyceride levels to less 
than 1000 mg/dL, through dietary restriction of fat and 
lipid-lowering medications (mainly fibric acid derivatives: 
fenofibrate). Such a reduction has been proved to prevent 
from recurrent episodes of AP, whereas there are anecdotal 
reports of other therapies, such as plasmapheresis. 
CONSENT 
Apollo Medicine, Vol. 7, No. 4, December 2010 314 
Written informed consent was obtained from the patient 
for publication of this case report and accompanying 
images. 
REFERENCES 
1. Linares LC, Pelletier AL, Czernichow S, Vergnaud AC, 
Bonnefont-Rousselot D, Levy P, et al. Acute pancreatitis in 
a cohort of 129 patients referred for severe 
hypertriglyceridemia. Pancreas. 2008; 37(1):13. 
2. Tsuang W, Navaneethan U, Ruiz L, Palascak JB, Gelrud 
A: Hypertriglyceridemic pancreatitis: presentation and 
management. Am J Gastoenterol. 2009; 104(4): 984-991 
3. Frank B, Gottlieb K. Amylase normal, lipase elevated: Is it 
pancreatitis? A case series and review of the literature. Am 
J Gastroenterol. 1999; 94(2): 463-469. 
4. Yadav D, Pitchumoni CS. Issues in Hyperlipidemic 
pancreatitis. J Clin Gastroenterol; 2003; 261(1): 54-62.
Apollo hospitals: http://www.apollohospitals.com/ 
Twitter: https://twitter.com/HospitalsApollo 
Youtube: http://www.youtube.com/apollohospitalsindia 
Facebook: http://www.facebook.com/TheApolloHospitals 
Slideshare: http://www.slideshare.net/Apollo_Hospitals 
Linkedin: http://www.linkedin.com/company/apollo-hospitals 
BBlloogg:: http://www.letstalkhealth.in/

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Hypertriglyceridemia Induced Pancreatitis

  • 2. Case Report Department of Gastroenterology, Apollo Hospitals, Greams Road, Chennai 600 006, India. Correspondence: Dr K R Palaniswamy, Senior Consultant, Department of Gastroenterology, Apollo Hospitals, Background: A 32 year-old female presented to the emergency department complaining of 12 hours upper abdominal pain accompanied by 2-3 episodes of vomiting.Case report: The patient had a heavy meal a few hours before. There were no signs of peritonitis. Routine laboratory examinations revealed leukocytosis, hyperglycemia and hyperamylasemia (serum amylase: 336 mg/dL).Conclusion:The lipid profile revealed an impressive elevation of triglycerides (4240 mg/dL). The serum was extremely lipemic. The abdomen computed tomography confirmed the diagnosis of pancreatitis. CASE REPORT HYPERTRIGLYCERIDEMIA INDUCED PANCREATITIS Bhavesh Thakkar, V Seshadri and KR Palaniswamy Greams Road, Chennai 600 006, India. A 32 year-old female presented to the emergency department complaining of 12 hour upper abdominal pain accompanied by 2-3 episodes of vomiting. She was a known diabetic for 4 years and had 2 episodes of pancreatitis in past. She was on oral hypoglycaemic agents and statins for the same. She had no history of gallstone disease or alcohol intake. The patient’s physical examination revealed a mild upper abdominal tenderness. There were no signs of peritonitis. The rest of the clinical examination was normal. Her vital signs were: Blood Pressure: 120/80 mmHg, Heart rate: 86 bpm. Respiratory Rate: 26 breaths/min, Temperature: 99ºF, Pulse Oximetry: 95% (on air). Routine laboratory examinations revealed leukocytosis (WBC: 13,3 K/μL), hyperglycemia (378 mg/ dL) and hyperamylasemia (serum amylase: 336 mg/dL). BMI was 33.75 kgr/m2. The lipid profile revealed an impressive elevation of triglycerides (4240 mg/dL) and cholesterol (325 mg/dL) levels. The serum was extremely lipemic (Fig 1). The abdomen computed tomography confirmed the diagnosis of pancreatitis. The patient was admitted for further evaluation and treat-ment.She was managed conservatively with iv hydration and dietary restriction. Moreover, she was admitted to the ICU for 3 days as she developed severe acidosis and respiratory compromise. The patient was treated with rapid acting insulin for 2 days during admission and underwent two sessions of plasmapheresis, in order to achieve quick improvement of triglyceride levels. She was restarted on lipid-lowering medications (atorvastatin, fenofibrate). Her clinical condition improved significantly with NIV and plasmapheresis and the patient was discharged in good health 15 days later, with a triglyceride level of 324 mg/dL. Uncontrolled diabetes with hypertriglyceridemia was probably the cause of this episode of acute pancreatitis. Hypertriglyceridemia is a relatively uncommon cause of pancreatitis [1]. Pancreatitis secondary to hypertriglyceri-demia typically presents as an episode of acute pancreatitis (AP) or recurrent pancreatitis and rarely as chronic pancreatitis [1,2]. An important and usually identifiable risk factor is a serum triglycerides level of 1000-2000 mg/dL in a patient with an already known type I, IV or V hyperlipidemia (Fredrickson’s classification). The typical clinical profile is a patient presenting with a preexisting lipid abnormality in combination with a secondary co-releasing factor, such as poorly controlled Fig 1 Lipemic serum- picture after plasmapheresis. 313 Apollo Medicine, Vol. 7, No. 4, December 2010
  • 3. Case Report diabetes mellitus, medications related to induction of AP or alcohol consumption. In addition to the usual findings in AP, in Hyperlipidemic Pancreatitis (HLP), the serum pancreatic enzymes may be normal or slightly elevated [3], even in the presence of severe AP that has been confirmed by imaging techniques [2,4]. The diagnostic hallmark consists of a mildly elevated amylase with interestingly low urine amylase levels along with the presence of lipemic serum in a patient with a family history of disturbed lipid profile [1]. As far as it concerns the clinical course of HLP, it does resemble to that of AP derived from other causes, with similar complications but not in a higher rate than in other types of AP. Routine management should not differ much, aiming at a reduction of triglyceride levels to less than 1000 mg/dL, through dietary restriction of fat and lipid-lowering medications (mainly fibric acid derivatives: fenofibrate). Such a reduction has been proved to prevent from recurrent episodes of AP, whereas there are anecdotal reports of other therapies, such as plasmapheresis. CONSENT Apollo Medicine, Vol. 7, No. 4, December 2010 314 Written informed consent was obtained from the patient for publication of this case report and accompanying images. REFERENCES 1. Linares LC, Pelletier AL, Czernichow S, Vergnaud AC, Bonnefont-Rousselot D, Levy P, et al. Acute pancreatitis in a cohort of 129 patients referred for severe hypertriglyceridemia. Pancreas. 2008; 37(1):13. 2. Tsuang W, Navaneethan U, Ruiz L, Palascak JB, Gelrud A: Hypertriglyceridemic pancreatitis: presentation and management. Am J Gastoenterol. 2009; 104(4): 984-991 3. Frank B, Gottlieb K. Amylase normal, lipase elevated: Is it pancreatitis? A case series and review of the literature. Am J Gastroenterol. 1999; 94(2): 463-469. 4. Yadav D, Pitchumoni CS. Issues in Hyperlipidemic pancreatitis. J Clin Gastroenterol; 2003; 261(1): 54-62.
  • 4. Apollo hospitals: http://www.apollohospitals.com/ Twitter: https://twitter.com/HospitalsApollo Youtube: http://www.youtube.com/apollohospitalsindia Facebook: http://www.facebook.com/TheApolloHospitals Slideshare: http://www.slideshare.net/Apollo_Hospitals Linkedin: http://www.linkedin.com/company/apollo-hospitals BBlloogg:: http://www.letstalkhealth.in/