1) The pancreas develops from two buds, the dorsal and ventral buds, which arise from the duodenum and fuse during development.
2) CT is the preferred imaging modality for evaluating acute pancreatitis to confirm the diagnosis, assess severity and complications such as necrosis, pseudocysts and fluid collections.
3) Acute pancreatitis is classified on CT imaging as interstitial edematous pancreatitis or necrotizing pancreatitis depending on the presence of pancreatic or peripancreatic necrosis. CT also guides management by identifying complications.
In this presentation the development of Small intestine and Pancreas has been discussed. The viewer would be able to understand the concept of physiological herniation and rotation of the Primary intestinal loop with in the connecting stalk.
In this presentation the development of Small intestine and Pancreas has been discussed. The viewer would be able to understand the concept of physiological herniation and rotation of the Primary intestinal loop with in the connecting stalk.
This presentation provides a comprehensive review of major sulci of brain which help in defining the different lobes of brain.Very useful for first year residents.
This presentation provides a comprehensive review of major sulci of brain which help in defining the different lobes of brain.Very useful for first year residents.
CE Title: Gastrointestinal Bleeding Scintigraphy: Changing the Paradigm
Presented at the Annual Meeting of the Society of Nuclear Medicine and Molecular Imaging, held in Denver, CO on Tuesday, June 13, 2017, 8:00 AM–9:30 AM
Educational Objectives
Upon completion of this activity, the participant will be able to:
1. Interpret GIBS images, planar and SPECT/CT.
2. Compare GIBS with available diagnostic tests used in GI bleeding, including GIB-CTA, endoscopy, etc.
3. Implement the best practice technique for GIBS, based on the revised SNMMI guideline document.
Sonological features of Pancreatitis.pptxvinodkrish2
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Acute pancreatitis
Last revised by Rohit Sharma on 27 Sep 2023
Citation, DOI, disclosures and article data
Acute pancreatitis (plural: pancreatitides) is an acute inflammation of the pancreas and potentially life-threatening.
On this page:
Article:
Terminology
Epidemiology
Diagnosis
Clinical presentation
Pathology
Radiographic features
Treatment and prognosis
Differential diagnosis
See also
Related articles
References
Images:
Cases and figures
Terminology
Two subtypes of acute pancreatitis are described in the Revised Atlanta Classification 1:
interstitial edematous pancreatitis
the vast majority (90-95%)
most often referred to simply as "acute pancreatitis" or "uncomplicated pancreatitis"
necrotizing pancreatitis
necrosis develops within the pancreas and/or peripancreatic tissue
Epidemiology
The demographics of patients affected by acute pancreatitis reflect the underlying cause, of which there are many (see Pathology below).
Diagnosis
The diagnosis of acute pancreatitis is usually based on clinical criteria or a combination of clinical and radiographic features 1.
Diagnostic criteria
Two of the following three criteria are required for the diagnosis 1:
acute onset of persistent, severe epigastric pain (i.e. pain consistent with acute pancreatitis)
lipase/amylase elevation >3 times the upper limit of normal
characteristic imaging features on contrast-enhanced CT, MRI, or ultrasound
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Clinical presentation
Classical clinical features include 3:
acute onset of severe central epigastric pain (over 30-60 min)
poorly localized tenderness and pain
exacerbated by supine positioning
radiates through to the back in 50% of patients
Elevation of serum amylase and lipase are 90-95% specific for the diagnosis 3.
A normal amylase level (normoamylasaemia) in acute pancreatitis is well-recognized, especially when it occurs on the ground of chronic pancreatitis. A normal lipase level has also been reported (<10 case reports) but is extremely rare 16.
(Rare) signs of hemorrhage on the physical exam include:
Cullen sign: periumbilical bruising
Grey-Turner sign: flank bruising
Pathology
There continues to be debate over the precipitating factor leading to acute pancreatitis, with duct occlusion being an important factor, but neither necessary nor sufficient.
Mechanism notwithstanding, activation of pancreatic enzymes within the pancreas rather than the bowel leads to inflammation of the pancreatic tissue, disruption of small pancreatic ducts, and leakage of pancreatic secretions. Because the pancreas lacks a capsule, the pancreatic juices have ready access to surrounding tissues. Pancreatic enzymes digest fascial layers, spreading the inflammatory process to multiple anatomic compartments.
Etiology
gallstone passage/impaction: most common cause of acute pancreatitis (up to 15% develo
Annular pancreas is an uncommon condition in adults.
The ring formation generally originates from the failure of
normal clockwise rotation of ventral pancreas. First
described by Tiedmann in 1818, its incidence is
1:20,000 population. It has bimodal presentation i.e is seen
either in Infants or in 4th & 5th decade of life.
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RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
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TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
3. DEVELOPMENT OFDEVELOPMENT OF
PANCREASPANCREAS
• The pancreas develops in two parts, both ofThe pancreas develops in two parts, both of
which arise from the endoderm of the primitivewhich arise from the endoderm of the primitive
duodenum.duodenum.
• The dorsal bud is the first to appear, as aThe dorsal bud is the first to appear, as a
diverticulum from the dorsal wall of thediverticulum from the dorsal wall of the
duodenum. This eventually forms the whole ofduodenum. This eventually forms the whole of
the neck, body and tail of the gland, togetherthe neck, body and tail of the gland, together
with part of the head.with part of the head.
4. • The ventral bud develops more caudally as aThe ventral bud develops more caudally as a
diverticulum from the developing bile duct atdiverticulum from the developing bile duct at
the point where the latter opens into thethe point where the latter opens into the
duodenum.duodenum.
5.
6. • Soon after the appearance of the two parts, theSoon after the appearance of the two parts, the
duodenum undergoes partial rotation and theyduodenum undergoes partial rotation and they
approximate each other and fuse. Until this stageapproximate each other and fuse. Until this stage
the dorsal duct, the duct of Santorini, opens intothe dorsal duct, the duct of Santorini, opens into
the duodenum proximal to the major papillathe duodenum proximal to the major papilla
(ampulla of Vater) at the minor papilla, whereas(ampulla of Vater) at the minor papilla, whereas
the ventral duct, the duct of Wirsung, which isthe ventral duct, the duct of Wirsung, which is
joined with the lower common bile duct, opensjoined with the lower common bile duct, opens
into the major papilla.into the major papilla.
7. • In the majority of cases, fusion of the two ductsIn the majority of cases, fusion of the two ducts
occurs at the junction of the head and body ofoccurs at the junction of the head and body of
the gland Thus the main pancreatic duct opensthe gland Thus the main pancreatic duct opens
into the major papillainto the major papilla
8. CONGENITAL ANAMOLIESCONGENITAL ANAMOLIES
• Pancreatic divisum: Pancreas divisum is thePancreatic divisum: Pancreas divisum is the
most common congenital pancreatic ductalmost common congenital pancreatic ductal
anatomic variantanatomic variant
• The abnormality results from failure of theThe abnormality results from failure of the
dorsal and ventral pancreatic anlage to fusedorsal and ventral pancreatic anlage to fuse
during the sixth to eighth weeks of gestationduring the sixth to eighth weeks of gestation
• MRCP provides a noninvasive means ofMRCP provides a noninvasive means of
diagnosing pancreas divisum without the use ofdiagnosing pancreas divisum without the use of
contrast material and avoids the risk of ERCP-contrast material and avoids the risk of ERCP-
induced pancreatitis.induced pancreatitis.
11. • ANNULAR PANCREAS: 2ANNULAR PANCREAS: 2ndnd
most commonmost common
anamoly in which a band of pancreatic tissueanamoly in which a band of pancreatic tissue
surrounds the descending duodenum, eithersurrounds the descending duodenum, either
completely or incompletely, and is in continuitycompletely or incompletely, and is in continuity
with the head of the pancreaswith the head of the pancreas
• CT or MR images may show normal pancreaticCT or MR images may show normal pancreatic
tissue, with or without a small pancreatic duct,tissue, with or without a small pancreatic duct,
encircling the duodenumencircling the duodenum
•
15. • ECTOPIC PANCREATIC TISSUE:EctopicECTOPIC PANCREATIC TISSUE:Ectopic
rests of pancreatic tissue are usually located inrests of pancreatic tissue are usually located in
either the submucosa of the gastric antrum oreither the submucosa of the gastric antrum or
the proximal portion of the duodenumthe proximal portion of the duodenum
Variations of Pancreatic Ducts:A bifidVariations of Pancreatic Ducts:A bifid
pancreatic duct is an anomaly in which the mainpancreatic duct is an anomaly in which the main
pancreatic duct is bifurcated along its lengthpancreatic duct is bifurcated along its length
17. INDICATIONS OF IMAGINGINDICATIONS OF IMAGING
The clinical signs of acute pancreatitis areThe clinical signs of acute pancreatitis are
nonspecific, with serum amylase and lipase levelsnonspecific, with serum amylase and lipase levels
correlating poorly with disease severity .correlating poorly with disease severity .
Elevated plasma serum amylase and lipase levelsElevated plasma serum amylase and lipase levels
are not specific to acute pancreatitis and may beare not specific to acute pancreatitis and may be
elevated by bowel obstruction, infarction,elevated by bowel obstruction, infarction,
cholecystitis, and perforated ulcer. Imaging ischolecystitis, and perforated ulcer. Imaging is
recommended to confirm the clinical diagnosis,recommended to confirm the clinical diagnosis,
diagnose its cause, exclude alternative causes ofdiagnose its cause, exclude alternative causes of
abdominal pain, and grade the extent andabdominal pain, and grade the extent and
severity of acute pancreatitisseverity of acute pancreatitis
18. Acute PancreatitisAcute Pancreatitis
PathophysiologyPathophysiology
• Blockage of the pancreatic duct leads to increasedBlockage of the pancreatic duct leads to increased
pressure in pancreatic duct and rupture.pressure in pancreatic duct and rupture.
• Pancreatic fluid (proteolytic and lipolytic enzymes)Pancreatic fluid (proteolytic and lipolytic enzymes)
ruptures into pancreas parenchyma and anteriorruptures into pancreas parenchyma and anterior
pararenal spacepararenal space
Gore and Levine,
Textbook of
Gastrointestinal Radiology
19. IMAGING MODALITIESIMAGING MODALITIES
Imaging of pancreasImaging of pancreas
• Radiograph– detect calcification (practically ofRadiograph– detect calcification (practically of
no help)no help)
• USG – differentiation of cystic and solid lesionsUSG – differentiation of cystic and solid lesions
(screening tool & for follow-up)(screening tool & for follow-up)
• CT scan – modality of choiceCT scan – modality of choice
• MRI and MRCP – complimentary to CTMRI and MRCP – complimentary to CT
20. Imaging Goals in PancreatitisImaging Goals in Pancreatitis
1.1. Exclude other abdominal disorders that canExclude other abdominal disorders that can
mimic acute pancreatitismimic acute pancreatitis
– DDx: acute cholecystitis, bowel obstruction orDDx: acute cholecystitis, bowel obstruction or
infarction, perforated viscus, renal colic, duodenalinfarction, perforated viscus, renal colic, duodenal
diverticulitis, aortic dissection, appendicitis, anddiverticulitis, aortic dissection, appendicitis, and
ruptured abdominal aortic aneurysmruptured abdominal aortic aneurysm
1.1. Confirm clinical diagnosis of acuteConfirm clinical diagnosis of acute
pancreatitispancreatitis
2.2. Staging the disease, by evaluation of theStaging the disease, by evaluation of the
extent and nature of pancreatic injury andextent and nature of pancreatic injury and
peripancreatic inflammationperipancreatic inflammation
21. TYPESTYPES
• The revised Atlanta classification (2012) ofThe revised Atlanta classification (2012) of
acute pancreatitis divides the condition intoacute pancreatitis divides the condition into
• interstitial oedematous pancreatitis andinterstitial oedematous pancreatitis and
necrotising pancreatitis, (formerly termed mildnecrotising pancreatitis, (formerly termed mild
and severe acute pancreatitis).Thisand severe acute pancreatitis).This
morphological classification system is based onmorphological classification system is based on
findings on contrast-enhanced CTfindings on contrast-enhanced CT
22. Interstitial OedematousInterstitial Oedematous
PancreatitisPancreatitis
• imaging findings in interstitial oedematousimaging findings in interstitial oedematous
pancreatitis include focal or diffuse enlargementpancreatitis include focal or diffuse enlargement
of the gland, with normal homogeneousof the gland, with normal homogeneous
enhancement or slightly heterogeneousenhancement or slightly heterogeneous
enhancement of the pancreatic parenchyma,enhancement of the pancreatic parenchyma,
which is attributable to oedema.which is attributable to oedema.
23. Necrotising PancreatitisNecrotising Pancreatitis
• This is the hallmark of severe acute pancreatitis.This is the hallmark of severe acute pancreatitis.
The revised Atlanta classification distinguishesThe revised Atlanta classification distinguishes
three forms of acute necrotising pancreatitis:three forms of acute necrotising pancreatitis:
pancreatic parenchymal necrosis alone,pancreatic parenchymal necrosis alone,
peripancreatic necrosis alone, and pancreaticperipancreatic necrosis alone, and pancreatic
necrosis with peripancreatic necrosis. All threenecrosis with peripancreatic necrosis. All three
types can be sterile or infectedtypes can be sterile or infected
24. Abdominal Plain FilmAbdominal Plain Film
Findings of AcuteFindings of Acute
Pancreatitis onPancreatitis on
Abdominal Plain FilmAbdominal Plain Film
– Duodenal ileusDuodenal ileus
– Colon cutoff (paucity ofColon cutoff (paucity of
gas distal to splenicgas distal to splenic
flexure due to spasm offlexure due to spasm of
colon affected by spreadcolon affected by spread
of pancreaticof pancreatic
inflammation)inflammation)
– Pancreatic abscess (gasPancreatic abscess (gas
bubbles)bubbles)
– Gasless abdomen due toGasless abdomen due to
excessive vomitting.excessive vomitting.
– Loss of psoas shadow.Loss of psoas shadow.
25. Plain Chest FilmPlain Chest Film
• Findings of Acute PancreatitisFindings of Acute Pancreatitis
on Plain Chest Film:on Plain Chest Film:
Left sided pleural effusions (seenLeft sided pleural effusions (seen
on 10% of chest films)on 10% of chest films)
– basal atelectasisbasal atelectasis
– pulmonary infiltratespulmonary infiltrates
– Splinting of left diaphragm andSplinting of left diaphragm and
basal parenchymabasal parenchyma
27. UltrasoundUltrasound
• IndicationsIndications
– Good screening test in mild disease, suspected biliaryGood screening test in mild disease, suspected biliary
pancreatitispancreatitis
• UsesUses
– Detection of gallstonesDetection of gallstones
– Bile duct obstructionBile duct obstruction
– Follow up of pseudocystsFollow up of pseudocysts
– diagnosis of vascular complications, i.e. thrombosisdiagnosis of vascular complications, i.e. thrombosis
• Major LimitationsMajor Limitations
– Bowel gasBowel gas
– US cannot specifically reveal areas of necrosisUS cannot specifically reveal areas of necrosis
28. Ultrasound findingsUltrasound findings
• Enlargement of pancreas- Universal but notEnlargement of pancreas- Universal but not
specific , upper limit of normal pancreaticspecific , upper limit of normal pancreatic
thickness=22 mmthickness=22 mm
• Pancreatic echogenicty(subjective) decreases duePancreatic echogenicty(subjective) decreases due
to oedema but sometime rarely can be increasedto oedema but sometime rarely can be increased
due to haemorrhage, necrosis, fat saponification.due to haemorrhage, necrosis, fat saponification.
• ““pseudopancreatitis”- pacreatic echogencitypseudopancreatitis”- pacreatic echogencity
decreased due to fatty filtration.decreased due to fatty filtration.
29. • Pancreatic inflammation- hypoechoic/ anechoicPancreatic inflammation- hypoechoic/ anechoic
• Difficult to distinguish inflammaton from fluidDifficult to distinguish inflammaton from fluid
• Ventral and adjacent to pancreas in pre-Ventral and adjacent to pancreas in pre-
pancreatic retroperitoneum, rt and left antpancreatic retroperitoneum, rt and left ant
pararenal spaces, perinal spaces, transversepararenal spaces, perinal spaces, transverse
mesocolon.mesocolon.
• But fluid is more localised,thicker, causemassBut fluid is more localised,thicker, causemass
effecteffect
30. CT FINDINGSCT FINDINGS
• CT is the imaging modality of choice for theCT is the imaging modality of choice for the
diagnosis and staging of acute pancreatitis anddiagnosis and staging of acute pancreatitis and
its complications.its complications.
32. Targets of Inflammatory spreadTargets of Inflammatory spread
in Acute Pancreatitisin Acute Pancreatitis
• 1= spread into the lesser1= spread into the lesser
sacsac
• 2 = spread into the2 = spread into the
transverse mesocolontransverse mesocolon
• 3 = spread into the root3 = spread into the root
of the bowel mesenteryof the bowel mesentery
• 4 = extension into the4 = extension into the
duodenumduodenum
• 5= inferior spread into5= inferior spread into
the remainder anteriorthe remainder anterior
pararenal spacepararenal space
• 6=RP fluid colecting6=RP fluid colecting
down to scrotum,or evendown to scrotum,or even
thighthigh
Gore and Levine, Textbook of Gastrointestinal Radiology
34. Computed TomographyComputed Tomography
““CT is the premier imaging test in the diagnosisCT is the premier imaging test in the diagnosis
and management of patients with acuteand management of patients with acute
pancreatitis. It visualizes the gland, thepancreatitis. It visualizes the gland, the
retroperitoneum, the abdominal ligaments, theretroperitoneum, the abdominal ligaments, the
mesenteries, and the omenta in their entirety.”mesenteries, and the omenta in their entirety.”
41. Normal Bowel
Wall Edematous,
Inflamed Bowel
Wall
Inflamed Fat
Normal Fat
Inflammation Spreads to the Transverse ColonInflammation Spreads to the Transverse Colon
46. • Total scoreTotal score
• Total points are given out of 10 to determineTotal points are given out of 10 to determine
the grade of pancreatitis and aid treatment:the grade of pancreatitis and aid treatment:
• 0-2: mild0-2: mild
• 4-6: moderate4-6: moderate
• 8-10: severe8-10: severe
•
47. Fluid collectns assc with acuteFluid collectns assc with acute
pancreatitispancreatitis
APFCAPFC
Acute Peripancreatic Fluid Collections containAcute Peripancreatic Fluid Collections contain
fluid only and are not or only partiallyfluid only and are not or only partially
encapsulated. They are seen within 4 weeks inencapsulated. They are seen within 4 weeks in
interstitial pancreatitisinterstitial pancreatitis
• ANCANC
Acute Necrotic Collections contain a mixture ofAcute Necrotic Collections contain a mixture of
fluid and necrotic material. They are not or onlyfluid and necrotic material. They are not or only
partially encapsulated. They are seen within 4partially encapsulated. They are seen within 4
weeks in necrotizing pancreatitis.weeks in necrotizing pancreatitis.
48. • PseudocystPseudocyst
After 4 weeks in interstitial pancreatitis. ThisAfter 4 weeks in interstitial pancreatitis. This
fluid collection is encapsulated. Most persistentfluid collection is encapsulated. Most persistent
fluid collections also contain some necroticfluid collections also contain some necrotic
material.material.
• WONWON
After 4 weeks most necrotic collections are fullyAfter 4 weeks most necrotic collections are fully
encapsulated, heterogenous non_liquefiedencapsulated, heterogenous non_liquefied
material and are called Walled-off Necrosismaterial and are called Walled-off Necrosis
(WON).(WON).
49. CHRONIC PANCREATITISCHRONIC PANCREATITIS
• Chronic pancreatitis occurs due to intermittentChronic pancreatitis occurs due to intermittent
pancreatic inflamation with progressivepancreatic inflamation with progressive
irreversible dilation to the glandirreversible dilation to the gland
• Alcholoism is the most common etiologyAlcholoism is the most common etiology
• HALL MARK imaging feature: ductal dilationHALL MARK imaging feature: ductal dilation
along with calcificationsalong with calcifications
• Other featurs areatrophic gland, focal necrosisOther featurs areatrophic gland, focal necrosis
ascites and pleural effusion formationascites and pleural effusion formation
50. • Pseudocysts are morePseudocysts are more
common in chroniccommon in chronic
thaan in acutethaan in acute
pancreatitis.pancreatitis.
• xray: calcifications canxray: calcifications can
be visualised in halfbe visualised in half
of the patients wthof the patients wth
alcohol etiologyalcohol etiology
53. GROOVE PANCREATITISGROOVE PANCREATITIS
• Distinct form of chronic pancreatitis affectingDistinct form of chronic pancreatitis affecting
groove between pancreatic head, duodenum andgroove between pancreatic head, duodenum and
CBD.CBD.
• CT: plate like hypoattenuating lesion locatedCT: plate like hypoattenuating lesion located
between pancreatic head and decending part ofbetween pancreatic head and decending part of
duodenum.duodenum.
• MRCP: hypovascular lesion and pathognomicMRCP: hypovascular lesion and pathognomic
cystic changescystic changes
54. AUTO IMMUNEAUTO IMMUNE
• Another distinct form of chronic pancreatitisAnother distinct form of chronic pancreatitis
• Typically affects patients without a history ofTypically affects patients without a history of
alcohol abuse and biliary stone disease.alcohol abuse and biliary stone disease.
• Gland shows infiltration by CD4 T lymphocytesGland shows infiltration by CD4 T lymphocytes
and plasma cells.and plasma cells.
• CT/MRI: Diffuse/focal gland enlargementCT/MRI: Diffuse/focal gland enlargement
Narrowing of pancreaticNarrowing of pancreatic
ductduct
Delayed contrast enhancementDelayed contrast enhancement
1= spread into the lesser sac will deform the poserior gastric wall
2 = spread into the transverse mesocolon will cause deformity along the inferior border of the colon
3 = spread into the root of the bowel mesentery will cause deformity of the small bowel loops
4 = extension into the duodenum will cuse deformity and mucosal abnormalities
5= spread into the remainder of the retroperitoneum will cause changes in the anterior pararenal space