Professional Documents
Culture Documents
KARNATAKA.
BY
In Partial fulfillment
of the requirements for the degree of
DOCTOR OF MEDICINE
IN
RADIO-DIAGNOSIS
DEPARTMENT OF RADIO-DIAGNOSIS
J.J.M. MEDICAL COLLEGE
DAVANGERE – 577 004.
2014
i
ACKNOWLEDGEMENT
the ALMIGHTY GOD for giving me the strength both mentally and physically
Mr. I.M. SINGH and Mrs. JALE SANYII, who are my strength, for there
efforts and hardships they have been through which make me stand where I am
today.
College, Davangere for preparing for this task, guiding me with his superb
talent and professional expertise, showing great care and attention to details
and without his supervision and guidance this dissertation would have been
impossible.
D.M.R.D., Dr. JEEVIKA M.U. M.D., Dr. KIRAN KUMAR .S. HEGDE
M.D., Dr. BHAGYAVATHI M.D., Dr. SIDDESH M.D., Dr. NAVEEN .S.
encouragement.
vi
LIST OF ABBREVATIONS USED
Ca Carcinoma
CBD Common Bile Duct
CHD Common Hepatic Duct
CT Computed Tomography
ERCP Endoscopic Retrograde Cholangiopancreatography
FLASH Fast Low Angle Shot
FN False Negative
FOV Field Of View
FP False Positive
GB Gall Bladder
HASTE Half Fourier Acquisition Single Shot Turbo Spin Echo
MIP Maximum Intensity Projection
MRCP Magnetic Resonance Cholangiopancreatography
MRI Magnetic Resonance Imaging
NPV Negative Predictive Value
PPV Positive Predictive Value
RARE Rapid Acquisition With Relaxation Enhancement
SEN Sensitivity
SPE Specificity
TE Time Of Excitation
TN True Negative
TP True Positive
TR Time Of Relaxation
TSE Turbo Spin Echo
US/USG Ultrasonography
viii
ABSTRACT
BACKGROUND & OBJECTIVE:
The main objective of the study is to determine the accuracy of MRCP over
USG and CT in the evaluation of patients with obstructive jaundice.
MATERIAL & METHODS:
The study was conducted in the department of Radio Diagnosis, for a period
of 2 years from August 2011-August 2013. Thirty six patients were included in the
study. All the patients were referred to the department of radio diagnosis with the
clinical suspicion of obstructive jaundice and elevated serum bilirubin levels.
Ultrasonography followed by CT and then MRCP were done in all the patients. Three
experienced radiologists reviewed the images separately and evaluated the cause and
site of obstruction in these patients. The accuracy of each modality was analyzed
statistically and correlation was made with the surgical findings or histopathological
reports.
RESULTS:
Of the thirty six patients, sixteen patients had benign causes of obstructive
jaundice while twenty patients had malignant causes of obstructive jaundice. For
diagnosing the cause of obstructive jaundice MRI with MRCP has a greater diagnostic
accurancy of 94.4% than helical CT with accuracy of 91.6% and USG with diagnostic
accuracy of 30.56%.The sensitivity of MRI with MRCP is greater than that of helical
CT and USG in diagnosing the cause of obstructive jaundice. In diagnosing the site of
obstruction MRCP had a accuracy of 100% while CT had 88% and USG 55%. The
performance of MRCP when compared to CT and USG was statistically more
significant (p<0.05).
CONCLUSION:
In the diagnosis of obstructive jaundice and to know the cause, site and extent
of the lesion MRCP being a non invasive, non ionizing procedure seems to be a better
choice over other radiological procedures like USG, CT or ERCP. The only drawback
of MRCP is the cost involved and the availability. The limitation of the study is the
small sample size and that ERCP correlation for these patients was not done.
ix
TABLE OF CONTENTS
1. INTRODUCTION 01
2. OBJECTIVES 05
3. REVIEW OF LITERATURE 04
4. METHODOLOGY 30
5. PHOTOGRAPHS 35-45
6. RESULTS 46
7. DISCUSSION 59
8. CONCLUSION 64
9. SUMMARY 68
10. BIBLIOGRAPHY 70
11. ANNEXURES
• PROFORMA 78
• INFORMED CONSENT 83
• MASTER CHART 87
x
LIST OF TABLES
SL.
TABLES PAGE
NO.
xi
LIST OF GRAPHS
SL.
LIST OF GRAPHS PAGE NO.
NO.
xii
LIST OF PHOTOGRAPHS
SL. PAGE
PHOTOGRAPHS
NO. NO
xiii
INTRODUCTION
main goals of any imaging procedure in obstructive jaundice are to confirm the
presence of obstruction, its location, extent, probable cause, and it should also
attempt to obtain a map of biliary tree that will help the surgeon to determine
the best approach to each individual case. Among these Ultrasonography (USG)
imaging technique that has revolutionized the imaging of biliary and pancreatic
the biliary tree and pancreatic duct without injection of contrast materia 1 .
development of higher magnetic field strength and newer pulse sequences like
HASTE (Half Fourier Acquisition Single Shot Turbo Spin Echo) and RARE
1
MRCP shows the entire biliary tract and pancreatic duct without any
accuracy of MRCP suggests that, it has the potential to replace the more
invasive procedures like diagnostic ERCP, which should be used only in cases
the site and extent of the stenosis, the degree of proximal dilatation, the
pancreatic duct gives high signal intensity, while solid organs have low signal
intensity. On these images, the fluid of the biliary and pancreatic ducts gives
2
Drawbacks with ultrasonography and CT are, they do not accurately
advantage as follow:-
obstruction.
will help identify the nature of the disease (infection, tumor, calculus &
others), show the location and extent of involvement, suggest the type of
(medical and/or surgical), suggest surgical approach and help assess response
3
to the therapy. Rapid technical developments in coil design, gradient hardware,
with MRCP, Helical CT and ultrasonogrpahy who were suffering from various
diseases of biliary tract and/or pancreas and tried to evaluate the efficacy of
4
OBJECTIVES
5
REVIEW OF LITERATURE
to understand the broad spectrum of disorders that affect the biliary and
pancreatic system10 .
• Gall bladder
• Cystic duct
• Pancreatic duct
6
Intra hepatic bile ducts:
fewer in number and are randomly scattered throughout the liver.11 They are
linear water density structures seen along one side of portal vein. Towards the
hilum they unite to form right and left hepatic ducts which have a constant
location just anterior to main portal vein bifurcation.12 Normally intra hepatic
Two main ducts (right & left hepatic) issue from the liver and unite near
the right end of the porta hepatis to form the common hepatic duct; this is
slightly lateral to main portal vein. The common hepatic duct lies to the right
short axis diameter. The wall of CHD is normally visualized and measures less
than 1.5 mm and enhances brightly than adjacent pancreas. The CHD passes
downward for 3cm, and is joined on its right side at an acute angle by the cystic
duct. By the union of the common hepatic duct with cystic duct the common
bile duct is formed. CECT aids in differentiating water density CHD from the
Gall Bladder:
The Gall bladder is a pear shaped sac partly contained in a fossa on the
widest part and 30 to 50ml in capacity. It is divided into a fundus, body and
neck. The fundus or expanded end is directed downwards, forwards and to the
7
right. The body is directed upwards, backwards and to the left, near the right
end of the porta hepatis it is continuous with the neck. The neck is narrow, it
continuous with the cystic duct, at this point of continuity with the cystic duct
usually there is a constriction. The mucous membrane, which lines the neck
projects into its lumen in the form of oblique ridges, forming a sort of spiral
valve. From the right wall of the neck of the Gall bladder a small pouch, often
duct arises from its upper and left wall. There can be enhancement of normal
HU). Increase in density of lumen seen normally after post contrast. Signal
T1. Gallbladder wall appears thin and hypo intense relative to retroperitoneal
Cystic duct:
downwards and to the left from the neck of the gall bladder and joins the
common hepatic duct to form the common bile duct; it runs parallel with and
adheres to the common hepatic duct for a short distance before joining with it.
seen as small tubular fluid containing structure between gall bladder and bile
duct.10,13
8
Common bile duct:
Bile duct (CBD) is formed near the porta hepatis by the junction of the
cystic and common hepatic ducts; it is usually about 7.5cm long and about
6mm in diameter, and usually measures upto 8mm in short axis and the wall
downwards, backwards and slightly to the left & then it passes behind the
superior part of duodenum and then runs in a groove on the upper and lateral
part of the posterior surface of the head of the pancreas. At the left side of the
descending part of the duodenum the bile duct comes in contact with the
pancreatic duct and accompanies it into the wall of second part of duodenum
and there the two ducts usually unite to form hepatopancreatic ampulla, the
distal constricted end of this ampulla opens into the descending part of the
Pancreatic duct:
The main pancreatic duct courses cephalad, takes a 45-90 degree turn in
the neck and continues horizontally in the body and in the tail of the gland the
hepatopancreatic ampulla.10,13
like Gall bladder, cystic duct, hepatic duct, bile duct and pancreatic duct using
heavily T2 weighted spin echo images and gradient echo images with fat
saturation technique.
9
Fluid appears hyper intense on these sequences because of its long T2
relaxation time. Hence hepatobiliary tree including pancreatic duct will appear
bright within background of low signal intensity liver and other structures.
10
PATHOPHYSIOLOGY
biliary obstruction. The role of imaging is crucial for detection of site and
lesion and staging of the tumor is crucial to decide optimal management of the
with MRCP, it has the capacity to provide all in one evaluation of the suspected
obstructive lesions, obviating the need for any other investigation such as
CT/PTC/ERCP.
Aberrant duct is the only bile duct draining a particular hepatic segment.
The direct drainage of the right posterior duct into the common hepatic duct,
right or left sided, is a variant also known as the aberrant hepatic duct and is
It is the most common anatomic variation of biliary tree and constitutes the
Choledochal Cyst:
common in female than male patients. The precise origin of this abnormality is
11
ductal involvement and degree of dilatation, and it can be mild dilatation or a
large water density mass in the region of porta hepatic or adjacent to the head
Direct communication of cystic duct with the dilated duct is a must for
12
Caroli’s Disease:
appears as saccular cystic dilatation of the IHBDs. The cystic areas often
within dilated duct. ‘DOT’ represents portal radicle which enhances on post
contrast.12,13
Cholecystolithiasis:
b) Cholesterol stone
80%
c) Mixed stone
13
Mirizzi Syndrome:
fistulous type. On CT dilated bile ducts may be seen with the CHD dilated to
below the level of stone at neck or cystic duct. On MRCP simple type shows
gallbladder neck or cystic duct and in fistulous type there will be no smooth
lateral compression.12,13,19
intrahepatic bile ducts. Two subtypes, subtype1- perinatal type, subtype 2- fetal
type. Frequency of biliary atresia is less than 10 in 1 lakh live births. Obviously
Chronic Pancreatitis:
Calcification of the gland & duct can be seen along with dilatation of the duct
beyond its normal limits. Duct also shows multifocal stenosis, intraductal
14
decreased enhancement on contrast enhanced one. Helical CT shows pancreatic
enlargement.12,13
Choledocholithiasis:
formed in Gall bladder. Primary calculi arising de novo in the ducts are
2. Hepatobiliary parasitism
bile. 12,13,16,17
Cholangiocarcinoma:
in the liver. 2) hilar type (Klatskin tumor), originating from the confluence of
right & left hepatic duct. It constitutes 45% to 60% of cases 3) extra hepatic
15
type, originating form main hepatic ducts, common hepatic duct or CBD. It
may appear as unifocal, large mass, multifocal or diffuse infiltrative. Most are
65 years. Frequency in men is 1.5 times greater than in women. CECT has been
weighted images.
carcinoma of the head of the pancreas. Risk factors are smoking and alcohol
16
Ampullary Carcinoma :
seventh decade of life and is two times more common in men than in women.
It is the most common malignant neoplasm of the biliary tract. The peak
replacing gallbladder, with focal, asymmetric wall thickening ,and mass shows
cases were divided into four groups by anatomical segments. According to the
number of visualized hypo dense ring like structure produced by the dilated
bile duct as seen in axial sections made 1cm apart, Gall bladder size, dilation of
IHBR, and the pancreatic duct. Visualization of tumor masses and condition
like duct below the obstruction were other variable used to determine the level
17
Gibson N. Robert et al (1986) 23 in prospective study of 15 patients
with bile duct obstruction with various radiologic modalities, were compared
for their capability to demonstrate the level and cause of obstruction, and found
that US appears to be the single most useful modality in evaluation of bile duct
used the rapid sequence gradient echo acquisition with three-dimensional post
and 13 patients of obstructive jaundice. The results were compared with other
PTC or ERCP). Authors concluded that MRCP has the capability for non
invasive imaging of the biliary tree in patients with obstructive jaundice but
12 patients with malignancy related obstructive jaundice and the results were
later. Authors found dilatation and obstruction of the bile ducts were clearly
demonstrated in all patients on MRCP and there was 100% correlation with
18
PTBD gram. Authors concluded that though spatial resolution of 3D MR
performed with fast or turbo spin echo pulse sequence (FSE). These sequences
were not only slow and required longer scan time for adequate spatial
resolution but were also prone to motion induced artifacts and signal loss. The
latest imaging techniques for MRCP are Rapid Acquisition with relaxation
Echo (HASTE). 1,2 Using RARE and HASTE sequences, image acquisition is
during a single breath hold thus markedly reducing the motion artifacts and
that the best results were obtained by using a combination of 3D MIP and
technique for patients with suspected bile duct obstruction and equivocal
19
sonography and/or CT results and suggested that large prospective clinical
MRCP using HASTE sequence with ERCP or PTC. They showed that the
were easier to identify with HASTE-MRCP than with PTC or ERCP. They also
20
quick and high quality imaging of both normal and abnormal pancreaticobiliary
system.
proved that HASTE had high sensitivity for detecting stones in CBD and can
ERCP in patients with clinical episodes of bile duct calculi and in whom ERCP
was contraindicated.
pancreaticobiliary ductal disease proved that single shot MRCP was highly
sensitive (70 to 80%) and specific in detecting lesions in bile duct and
pancreatic duct.
94.1%). MRCP correctly showed the presence of bile duct dilatation and site of
studies. The only limitation of MRCP is its inability to offer any therapeutic
21
maneuver. Thus, it may significantly decrease the need for diagnostic ERCP.
diagnostic tests. Authors also pointed out that there is an additional value of
MRCP over ERCP and PTC as it shows an excellent quality cross sectional
images of liver and pancreas which are obtained in the same sitting, allowing
proved biliary diseases compared the efficacy of MRCP findings with ERCP
jaundice using MRCP concluded that there is a role for MRCP as a second line
jaundice.
with suspected bile duct disorders have proved that MRCP is highly accurate in
diagnosing the presence, level and cause of bile duct obstruction. They also
proved that MRCP is the investigation of choice for early diagnosis of biliary
22
atresia and it is non-invasive alternative in selected patients, in whom ERCP or
also proved that in comparison with surgical or ERCP findings, MRCP showed
biliary atresia and of 69% in the anomalous connections between the bile and
pancreatic ducts.
using single shot techniques, the most distal portion of the bile duct and
compared the efficacy of breath hold single shot fast spin echo (SSFSE)
tumor.
23
diagnostic information which was equivalent to that of ERCP. They also
showed that MRCP better defined the proximal biliary tree than ERCP,
however ERCP was superior in paediatric patients. They concluded that MRCP
the presence and level of biliary obstruction, and obstruction due to bile duct
related pathologies.
MRCP and sonogrpahy with ERCP. They proved MRCP was highly accurate
24
superior to sonography. They concluded that MRCP has a potential to replace
ERCP.
with suspected biliary disease. They concluded that unlike ERCP and PTC,
rarely required anesthesia. MRCP enables visualization of the entire liver and
of the biliary tree using MRCP HASTE and RARE sequences concluded that
anatomical variants of cystic duct and hepatic ducts, which are usually difficult
that MRCP can easily show anomalies and choledochocele on HASTE coronal
source images.
ERCP in 100 patients with biliary tract disease. They concluded that MRCP has
detection of bile duct diseases. They also proved that MRCP accurately
diagnosed the presence and level of strictures in all patients. The overall
were 97%, 98% and 97% respectively. They showed that MRCP diagnosed
with accuracy of 97%. They also noted that MRCP showed bile duct lesion in
25
all postoperative patients, whereas ERCP could not show either due to altered
MRCP has been found to be a simple, safe and highly accurate alternative to
period of 4 years using HASTE MRCP sequences. They concluded that HASTE
tree and pancreatic duct. Its multiplanar, fluid sensitive capability have
Gall Bladder stone and pancreatitis. HASTE MRCP also useful in identifying
D.R. Brine, R.L. Soulen (1999) 51 the role of MR imaging and MRCP is
evaluation with both ERCP & CT. They concluded that MRI with MRCP is a
safe and cost effective next step in the evaluation of patients with significant
concluded that MRCP using HASTE sequence was fast and accurate for
26
can reliably depict normal and diseased pancreaticobiliary ducts except for
or inadequate ERCP concluded that MRCP was found to have a unique and
SSFSE MRCP concluded that while single thick-slice MRCP only provided
components in and around the pancreas and showed their precise location.
intensity projection and thick section half Fourier Rapid Acquisition with
with volume rendered MR cholangiography was better than that with MIP and
cholangiography.
27
patients with malignant hilar and perihilar biliary obstruction and also
patients. All patients underwent PTC and 27 out of 29 patients also underwent
biliary drainage and/or stent placement within 7 days after MRCP. They
28
Bhatt C et al (2005)60 in their study of 50 patients with biliary and
pancreatic pathology determined that USG is the cheap and easily available
malignant from benign common bile duct stricture with multiphasic helical CT
portal phase is the main factor distinguishing malignant from benign CBD
strictures.
standard in biliary imaging proved that MRCP is highly sensitive and specific
for choledocholithiasis and avoids the need for invasive imaging in most
underwent MRI including MRCP, a fat suppressed T1 weighted fast low angle
shot sequence (FLASH) and an axial HASTE sequence who were enrolled in
the study, concluded that combining the axial T1 weighted image with MRCP
29
METHODOLOGY
patients suffering from various diseases of biliary tract and pancreas of all age
All the patients had undergone USG and most them have diagnosed on
The study protocol was approved by the ethical committee. All the
CT.
• All the patients were instructed to come with empty stomach on the day
of procedure.
30
Patient preparation for Helical CT:
• All the patients were instructed to come with empty stomach on the day
of procedure.
contrast CT.
• All patients clinical history were elicited to rule out previous contrast
reactions/allergies.
• All the patients were instructed to fast for 6 hours prior to examination.
was used.
METHODS:
and linear probes were used in the study. Images of the biliary tree were
Scanner. Patients were asked to drink 800 ml of diluted oral contrast 1 hour
performed to locate the pancreas. Contrast (80 ml, 300mg I/ml) was then
injected intravenously The scans were taken from diaphragm to iliac crest on
31
MRI-MRCP was performed on Philips ACHIVA 1.5 Tesla MRI
Scanner. Patient was given concentrated pineapple juice prior to scan. All
images were obtained with breath holding and parameters were individualized
No of Slice
TR TE Gap FOV
Sequence Slices Thickness Matrix
(ms) (ms) (mm) (mm)
(mm) (mm)
Ssh SPAIR COR 465 80 25 5 0.5 486 330
Ssh SPAIR TRA 425 80 40/35 5 0.5 420 330
Ssh SPAIR SAG 462 80 40 5 0.5 384 270
T2TSE HR TRA 2504 100 36 5 0.5 512 360
T1W 3D TSE 10 4.6 80 1.0 0.1 256 375
MRCP 3D HR 1204 650 110 1.0 0.8 512 266
Ssh MRCP RAD 8000 800 12 40 0.4 512 300
RT- Respiratory Triggering: bh- breath hold:
• Hepatic
• Suprapancreatic
• Pancreatic
• Ampullary
• Non visualized
• Definitely visualized.
32
3. Status of CBD
• Smooth tapering
• Abrupt end
• Rounded
• Irregular
• Minimal
• Moderate
• Marked
only)
DEFINITELY BENIGN:
PROBABLY BENIGN:
33
INCONCLUSIVE:
PROBABLY MALIGNANT:
tumor such as duct dilatation with ductal cut-off adjacent to the mass or
DEFINITELY MALIGNANT:
CBD dilatation with an abrupt narrowing located cranial to the level of mass
lesion.
surgery, five patients underwent cytology, and remaining with other modalities
34
ILLUSTRATION 1:
CASE OF CHOLELITHIASIS WITH CHOLEDOCHOLITHIASIS
USG CT
MRCP CECT
35
ILLUSTRATION 2
CASE OF CHOLEDOCHOCELE
USG CT
MRCP CECT
36
ILLUSTRATION 3
CASE OF MIRIZZI’S SYNDROME
CT CECT
MRCP
37
ILLUSTRATION 4
CASE OF CA HEAD OF PANCREAS
USG CECT
MRCP T2W MR
38
ILLUSTRATION 5
CASE OF KLATSKIN’S TUMOUR
MRCP
39
ILLUSTRATION 6
CASE OF CAROLI’S DISEASE
T2W COR
T2W AXIAL
MRCP
40
ILLUSTRATION 7
CASE OF LYMPHOMA
NECT
T2W (COR)
MRCP
41
ILLUSTRATION 8
CASE OF Gb MASS
42
ILLUSTRATION 9
CASE OF PERIAMPULLARY CARCINOMA
3D MRCP MRCP
43
ILLUSTRATION 10
CASE OF HYDATID CYST
MRCP MRCP
44
ILLUSTRATION 11
TYPE 1 CHOLEDOCAL CYST
ILLUSTRATION 12
TYPE 4A — CHOLEDOCAL CYST
ILLUSTRATION 13
SCLEROSING CHOLANGITIS
45
RESULTS
36 patients. The youngest patient of our study was 3 months old and the oldest
was 85 years. The mean age of patients with benign lesions was 37.4 years and
that with malignant lesions was 46.5 years. All the lesions were detected by
both CT and MRI with MRCP. CT characterized 15 patients had benign cause
be benign.
only 1 case (6.2%) turned out malignant, which was characterized benign by
17 (SPSS 17)”, software was used to analysed the datas and open epi software
accuracy. p-value was calculated by chi-square test, p-value less than 0.05 was
Sensitivity, Specificity, PPV, NPV, Accuracy was 18.75%, 40%, 20%, 38.1%,
30.56% for US, 87.5%, 95%, 93.33%, 90.48%, 91.67% for CT and 93.75%,
46
T able-1 : T able showiing Age diistribution
n of Study Subjects
In the
t study itt was obserrved that majority
m i.ee. 47.3% off the patien
nts with
with GB c arcinoma
Perccent
5.5
30.6 166.6
<122 years
13-330 years
31-660 years
47.3 60 Years
Y
47
Taable 2: Tab
ble showin
ng sex distrribution o f the studyy subjects
Sex No. of Pa
atients Percent
M
Male 19 53
F emale 17 47
T
Total 36 100
In the
t study it
i was obseerved that majority i..e. 53% off the patien
nts with
0%
4
47%
53% M
Male
F
Female
48
Table 3: Table sho wing type of lesion causing
c ob
bstructive jaundice among
a
t study subjects
the s
B
Benign 16 44
Maalignant 20 56
T
Total 36 100
In the
t study itt was obserrved that th
he most coommon cauuse for obsttructive
j
jaundice iss malignancy i.e. in 56%
5 of casees.
Perccent
0%
44%
56% Benign
Malignant
M
49
Table 4: Table show
wing beniggn causes for Obstru
uctive jaun
ndice amo
ong the
subjects
CBD
D calculi 4 25
Beniggn stricturee 4 25
Anatom
mic variannt 3 19
Choolangitis 1 6
T
Total 16 100
In the
t study it was obsserved thatt the mostt common benign caause for
25 25 25 25
20 19
15
10
6
0
D CALCULI
CBD CBD WITH
H GB ENIGN
BE ANATOMIIC CHOLA
ANGITIS
CALCU
ULI STR
RICTURE VARIANT
T
50
Table 5: Table sho wing maliignant cau
uses for Ob
bstructive jaundice among
a
the subjects
Malign
nant Causees No of cases
c Percent
Periam
mpullary C a 8 40
Cholanggiocarcinom
ma 4 20
C GB
Ca 4 20
Klatskkins tumorr 2 10
Ca headd of Pancreeas 1 5
Total 20
0 100
In the
t study i t was obseerved that the
t most c ommon maalignant caause for
40 40
35
30
25
20 20
20
15 10
10 5 5
5
0
51
Table 6: Table
T show
wing distr ibution off Benign an
nd Malign ant Lesion
ns with
respect to
t age
Age Groupp B
Benign Cas es Malignnant Cases Totaal cases
0-12 1 50 1 50 2
31-60 8 47 9 53 17
Total 16 20 36
X2=6.8, dff = 3, p=0. 078
In the
t study it
i was obseerved that malignant lesions w ere commo
on after
60yrs i.e. in
i 81.9%. Benign
B lesions were more
m comm
mon in the age group 1 to 30
90
833.3 81.9
80
70
60
53
50 50
50 47
40
30
16.7 18.1
20
10
0
0-12 13-30 31-660 >60
Benign Malignant
52
Table 7:: Table shoowing His topatholog
gical diagn
nosis amon
ng benign cases
Histop
pathologicaal Diagnossis No of ca ses Percen
nt
CB
BD benign stricture 4 25
CBD stoones 4 25
C
CBD & GB
B stones 4 25
C
Choledoch al cyst 2 12.5
Cholanggitis 1 6.25
Total 16 100
In the
t study it was obsserved thatt the mostt common benign caause for
in 75% of cases.
25 25 25 25
20
15
12.5
10
6.25 6.25
0
CBD D BENIGN C
CBD STONES CBD & GB CHOLEDOCHAL EXTRA
A CHOLAN
NGITIS
STTRICTURE STONES CYST HEPATIC
BILIARYY
ATRESIAA
casees
53
Table 8: Table
T show
wing Histoopathologiccal diagnoosis amongg malignan
nt cases
Histtopathologgical Diagn
nosis No of cases Percen
nt
Ad enocarcinooma duodennum 8 40
CB
BD Cholanngiocarcinooma 4 20
Adenocarccinoma GB
B 4 20
Hiilar Cholanngiocarcinooma 2 10
Addenocarcinnoma pancrreas 1 5
In the
t study i t was obseerved that the
t most c ommon maalignant caause for
40% of casses.
40 40
35
30
25
20 20
20
15
10
10 5 5
5
54
Table 9: Table
T show
wing diagn
nosis by Heelical CT scan
s and H
Histopatho
ological
diagno
osis.
Benign
n Ma
alignant
995% Confiidence
Limitt
Seensitivity 87.5%
8 63.98 - 96.5
9
Sp
pecificity 95% 76.39 - 99
9.11
Positive Predictive
P e Value 93.33%
9 70.18 - 98.81
96.00%
95%
94.00% 93.33%
92.00% 91.67%
90.48%
90.00%
87.50%
88.00%
86.00%
84.00%
82.00%
SENSITIVITYY SPECIFFICITY POSITIVE
P NEGATIVE DIAGNO
OSTIC
PR
REDICTIVE PREDICTIVE ACCURA
ACY
VALUE VALUE
55
Tablle 10: Tab le showingg diagnosi s by MRI with MRC
CP scan an
nd
Histop
pathologiccal diagnossis.
Histopatho
H ological
Significcance
diagno
osis
Beniign Malignant
M
MRI with
h Benign
n 15 (T
TP) 1 (FP) 16 X2 = 28.36
2
MRCP df = 1
Malignaant 1 (F N) 19 (TN) 20
p<
166 20 36 0.00000
00101
995% Confiidence
Limitt
Seensitivity 93.75%
9 71.67 - 98.89
Sp
pecificity 95% 76.39 - 99
9.11
Positive Predictive
P e Value 93.75%
9 71.67 - 98.89
Negative Predictivee Value 95% 76.39 - 99
9.11
Diagnoostic Accuracy 94.44%
9 81.86 - 98.46
95.20%
95.00% 95% 95%
94.80%
94.60%
94.44%
94.40%
94.20%
94.00%
93.75%
% 93.75%
93.80%
93.60%
93.40%
93.20%
93.00%
SENSITIVIT
TY SPECIF
FICITY PO
OSITIVE NEGATIVE DIAGNO
OSTIC
PRE
EDICTIVE E
PREDICTIVE ACCURAACY
VALUE
V VALUE
56
Tabl e 11: Tablle showingg diagnosiss by USG and
a Histop
pathologiccal
diagno
osis.
Histopath
hological
Signifi cance
diagn
nosis
Be nign Malignant
M t
Beniggn 13 8 21
USG X2 = 7.106
7
Inconclu
usive 3 8 11 df = 2
p < 0 .028
Malign
nant 0 4 4
16 20 36
995% Confiidence
Limitt
Seensitivity 18.75%
1 6.591 - 43
3.01
Sp
pecificity 40% 21.88 - 61.34
Positive Predictive
P e Value 20% 7.047 - 45.19
Negative Predictivee Value 38.1%
3 20.75 - 59
9.12
Diagnoostic Accuracy 30.56%
3 18 - 46 .86
40.00% 4
40%
38.10%
35.00%
30.56%
30.00%
25.00%
20%
18.75
5%
20.00%
15.00%
10.00%
5.00%
0.00%
SENSITIVITYY SPECIFFICITY POSITIVE
P NEGATIVE OSTIC
DIAGNO
PR
REDICTIVE PREDICTIVE ACCUR
RACY
VALUE VALUE
57
Table 122: Table s howing Coomparison
n of diagnoostic valuees of Helical CT
and MRI with MRC CP in causses of obsttructive ja undice
MRI with
h MRCP Helical C
CT USG
U
Seensitivity 93.75
5% 87.5% 18..75%
Sp
pecificity 95%
% 95% 4 0%
Positive Predictive
P Value 93.75
5% 93.33%
% 2 0%
80.00%
70.00%
60.00%
50.00%
40.00%
40%
30.00% 8.10%
38
20.00% 30.56%
18.75% 20%
10.00%
0.00%
SENSITIVITTY SPECIFICITY POSITIVE NEGATIV
VE DIAG
GNOSTIC
PREDICTIVE PREDICTIV
VE ACC
CURACY
VALUE VALUE
MR
RI with MRCP Helical CT USG
Figure 12:
1 Compaarison of diagnostic
d values
v of Helical
H CT
T and MRII with
M
MRCP in caauses of ob
bstructive jaundice
Fro m the abovve table it can be infferred that for diagnoosing the cause
c of
obstructivee jaundice , MRI witth MRCP has a gre ater diagn ostic accu
uracy of
accuracy of
o 30.56%.
and USG in
i diagnosiing the cauuse of obstrructive jaunndice.
58
DISCUSSION
their early stage is most important in patient care and management. Knowledge
invasive procedure like ERCP can be avoided solely for the purpose of
diagnosis.
of obstructive jaundice.
The youngest patient was 2 months old presented with choledocal cyst
and oldest patient was 85 yrs old with GB carcinoma. Maximum number of
patients (47.3%) were adults in the age group of 31-60yrs with 53% sufferers
were males. All of our cases presented with jaundice and abdominal pain. Most
USG was done in all the patients prior to Helical CT and MRI with
MRCP.USG was able to detect gall bladder calculi in all of the cases with
two patients, diagnosed clearly with CT and MR with 100% accuracy. This
shows that MR with MRCP is superior to USG in detecting CBD calculi and
1994; In their study they found an accuracy of 100% in detecting CBD calculi
59
In imaging of benign lesions( n=16) MR with MRCP diagnosed CBD
with GB calculi in all 8 patients with such a final diagnosis and CT also
showed the same in all and both the modalities showing 100% accuracy in
concordance with Soto et al 2000;In their study they found sensitivity of 94%
2006: In their study they found the sensitivity of diagnosing CBD calculus was
87% and our study showed that CT is more superior than their study 64 .
showed benign nature of stricture in all four cases approaching 100% accuracy.
MRCP showed clearly the length of the stricture segment very well and
concordance with Bhatt et al; In their study they found 100% accuracy for
MRCP in diagnosing benign CBD strictures. 60 One case of cholangitis has been
it as a benign lesion.
MR with MRCP. One case of biliary atresia and two cases of choledochal cysts.
60
Bhatt et al; In their study they found 100% accuracy for MRCP in diagnosing
anatomical variants 60 .
these cases MRCP demonstrated “double duct” sign which helped more in
arriving final diagnosis. One patient was diagnosed to have stricture disease
among the periampullary growth patients, due to technical fault and due to
diagnosed all four cases with a 100% accuracy with the help of conventional
61
2 patients were diagnosed to have Klatskins tumour , and the accuracy
2005;in their study they found accuracy of 100% for MRCP alone in
diagnosing Klatskins tumour 60 . But CT was not able to show exact extent of
two lesions as MRI did. Thus our study is in concordance with JK Han et al ;
resolution.
four cases with 100% accuracy, while CT showed positive finding in 3 cases,
with accuracy of 75% and one case it diagnosed as malignant hilar obstruction.
Conventional MRI added a lot once again in arriving final diagnosis. Among
these, two patient had liver metastasis shown clearly by both the modalities.
Our study is in concordance with Bhatt et al 2005 ; in their study they found an
ERCP correlation was got with one patient and findings were correlated
with MRCP and found that , MRCP findings were comparable to that of ERCP.
1988; in their study they found that MRCP images equivalent and better to
ERCP.28
62
pancreatic duct. A great advantage of ERCP is its ability to perform therapeutic
stent placement which will relieve obstruction. It requires a highly skilled and
choice in imaging patients with obstructive jaundice, and it becomes still more
• Non-operator dependant.
Like any other imaging modality MR with MRCP also has few
limitations.
Claustrophobia.
63
CONCLUSION
six patients of different ages and both sexes. Our study sought to define the
jaundice.
In our study, age ranged from 2 months to 85 years with mean age of 42
years. Most of our case was in the age group of 31-60 years. Males accounted
Among the benign cause of obstructive jaundice CBD calculi were the
52%.
common cause and constitutes about 40% of malignant causes. USG showed
43% and both CT and MR showed with 95% with 95% sensitivity in detecting
detecting malignant pathologies. But it is still MRCP that has potential role in
100% in accuracy.
During our study we observed that MRI with MRCP has 94% accuracy
Helical CT, MRI with MRCP is equally sensitive and more specific in
64
differentiating the causes of obstructive jaundice as malignant. MRI with
With the help of source image , we can very well show the exact
65
MR with MRCP is an accurate, non invasive means of evaluating the
It is useful in failed ERCP cases and it also shows biliary tree very well
pancreatic duct.
The diagnostic accuracy of MRI with MRCP suggests that it has the
contemplated.
strictures and to bile duct calculi. But still MRCP alone is more accurate than
enhanced MRI did not add any better performance to cross sectional MRI
combined with MRCP without contrast. From the above table it can be inferred
that for diagnosing the cause of obstructive jaundice MRI with MRCP has a
66
greater diagnostic accuracy of 94.4% than helical CT with accuracy of 91.6%
The sensitivity of MRI with MRCP is greater than that of helical CT and
67
SUMMARY
choice in imaging patients with obstructive jaundice, and it becomes still more
Like any other imaging modality MR with MRCP also has few
The diagnostic accuracy of MRI with MRCP suggests that it has the
contemplated.
and pancreatic duct. The only major hiccups in MRCP replacing all other
FUTURE:
pathology.
68
MRCP to
Obstructive jaundice exclude other
pathologies
Cholecystecomised patients
(dilated or non-dilated duct)
Intact gall bladder
CBD calculus
Ultrasound scan
Positive Negative
GB calculus No GB calculus
Therapeutic
Ductal calculus CBD ERCP
CBD
Conservative
Mx
Dilated Not dilated
MRCP or EUS
(To avoid diagnostic
ERCP)
Ductal calculus
Conservative
Therapeutic Positive
Mx
ERCP Negative
follow
Cholecystectomy Clinic follow-up
69
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28. Matthew A. Barish et al. MRCP: Efficacy of 3-D Turbo spin-echo
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77
PROFORMA
PATIENT’S NAME :
AGE :
SEX :
HOSPITAL NO :
WARD :
UNIT :
PARAMETERS:
HELICAL CT : DATE ( )
1. LEVEL OF OBSTRUCTION :
HEPATIC
SUPRA PANCREATIC
PANCREATIC
AMPULLARY
NON VISUALISED
POSSIBLE
DEFINITELY VISUALISED
78
3. STATUS OF DISTAL CBD :
SMOOTH TAPERING
ABRUPT END
ROUNDED
IRREGULAR
MINIMAL
MODERATE
MARKED
5. GALL BLADDER :
SIZE
WALL
STONES
PRESENT
ABSENT
7. PANCREAS :
ATROPHY
CALCIFICATIONS
PSEUDOCYSTS
8. MASS :
SOLID
CYSTIC
SOLID CYSTIC
ENHANCEMENT
79
9. VESSEL INVASION:
PRESENT
ABSENT
PRESENT
ABSENT
PRESENT
ABSENT
PRESENT
ABSENT
1 .LEVEL OF OBSTRUCTION :
HEPATIC
SUPRA PANCREATIC
PANCREATIC
AMPULLARY
80
3. STATUS OF DISTAL CBD :
SMOOTH TAPERING
ABRUPT END
ROUNDED
IRREGULAR
MINIMAL
MODERATE
MARKED
5. GALL BLADDER :
SIZE
WALL
STONES
PRESENT
ABSENT
7. PANCREAS:
ATROPHY
CALCIFICATIONS
PSEUDOCYSTS
8. MASS :
SOLID
CYSTIC
SOLID CYSTIC
ENHANCEMENT
81
9. VESSEL INVASION:
PRESENT
ABSENT
PRESENT
ABSENT
CONCLUSION
DEFINITELY BENIGN
PROBABLY BENIGN
PROBABLY MALIGNANT
DEFINITELY MALIGNANT
FINAL DIAGNOSIS :
ULTRASOUND :
HELICAL CT :
MRI WITH MRCP :
SURGICAL DIAGNOSIS :
DATE OF SURGERY :
DIAGNOSIS :
PATHOLOGICAL DIAGNOSIS :
HPE NO AND DATE :
DIAGNOSIS :
82
CONSENT FORM
Part 1 of 2
5. Name of Co Guide-
83
8. Procedure of the study:
will be performed first and following that MRI with MRCP will be
performed within 3 days with help of Philips 1.5 Tesla MRI Scanner.
contrast use.
consent.
14. Name of the contact person with official address and phone number:
Place:
Signature of investigator:
Date:
Witness:
84
CONSENT FORM
Part 2 of 2
The details of the study are provided to me in writing and have been
Form 1 of 2” giving the “Information for the patients of the study”. I fully
Name: Address:
85
KEY TO MASTER CHART :
A Abrupt end
Am Ampulla
B Benign
CD Cystic duct
D Dilated
F Female
GB Gall Bladder
H Hepatic
IC Inconclusive
M Malignant
N Normal
NV Non visualized
S Stricture
86
MASTER CHART
LEVEL OF DUCTAL STATUS IN DUCTAL STATUS IN DUCTAL STATUS IN
BILIRUBIN CALCULI NIGN/MALIGNA
OBSTRUCTION USG CT MRCP
AGE LOCAL EFFECT
S.NO NAME SEX IP NO FINAL DIAGNOSIS
(years) CD CBD GB /METASTASIS
INDIRECT
DIRECT
TOTAL
MRCP
MRCP
MRCP
MRCP
MRCP
IHBD
IHBR
IHBR
CHD
CHD
CHD
USG
USG
CBD
CBD
CBD
USG
USG
USG
PD
PD
PD
CD
CD
CD
CT
CT
CT
CT
CT
CHOLELITHIASIS WITH
1 Gangamma 34 F 754186 6.7 3.4 3.3 D NV NV D N D D D D N D D D D N A A A P P P P P P NIL B B B
CHOLEDOCHOLITHIASIS
ACUTE PANCREATITIS SEQUELAE
2 VEERAPPA 70 M 754997 6.5 3 3.5 N N N D N N N N D N N D D D N A A A A P P P P P NIL B B B WITH CHOLELITHIASIS &
CHOLEDOCHOLITHIASIS
KLATSKIN'S TUMOUR WITH
3 JANHBEE 63 F 755274 13.8 6.2 7.6 D NV NV N N D S NV S N D S NV S N A A A P P P P P P NIL IC B M CHOLELITHIASIS &
CHOLEDOCHOLITHIASIS
CYSTIC DUCT CALCULUS MIRIZZI'S SYNDROME WITH
4 VEERESH 22 M 755240 19.5 10.2 9.3 D D D N N D D D N N D D D N N P P P A A A P P P B B B
COMPRESSING CHD CHOLELITHIASIS
MASS AT HEAD OF
CA PANCREAS WITH FOCAL
5 KRISHNARMURTHY 51 M 755680 21 13.6 7.4 D NV NV D D D D NV D D D D A D D A A A A A A A A A PANCREAS CAUSING M M M
PANCREATITIS
COMPRESSION
6 KALPANA 42 F 755102 6.5 4.1 2.4 N N N N N N N N N N N N N N N A A A A A A P P P NIL B B B CHOLELITHIASIS
BENIGN STRICTURE ‐ DISTAL CBD
7 SURESH 30 M 754929 5.1 1.6 3.5 N N NV D N N N NV D N D+B D N S N A A A A A A A A A NIL IC IC B
WITH CHOLANGITIS
CHOLEDOCHOCELE WITH
8 HANIFAA BEE 65 F 755049 13.5 6.4 7.1 D D N D N D D N D N D D N D N A A A A A A A A A NIL IC B B
OBSTRUCTED CBD
CHOLANGIOCARCINOMA (DISTAL
9 LAKSHMI BAI 78 F 755080 14.1 8 6.1 D D N D N D D N D N D D N D+M N A P P A A A A A A NIL IC B M
CBD) WITH CYSTIC DUCT CALCULI
10 RAMESH 40 M 755081 10.5 3.1 7.4
11 KALYAN NAIK 52 F 755058 14.4 8.7 5.5 D NV NV N N D NV N N N D S N N N A A A A A A A A A NIL IC IC M KLATSKIN'S TUMOUR
GB FOSSA MASS
CAUSING EXTRANEOUS
12 SHARDAMMA 65 F 625817 16..5 8.8 7.7 D N N N N D C N C N D C N C N A A A A A A P P P B M M ADENOCARCINOMA OF GB
COMPRESSION OF CHD
& CBD
PERIAMPULLARY CA
EXTENDING INTO HEAD
PERIAMPULLARY CA WITH
13 KUBERAPPA 65 M 655081 12.7 5.1 7.6 D D N N N D D N S N D D N S N A A A A A A A A A OF PANCREAS , IC M M
METASTASIS
METASTASIS TO LN AND
VERTEBRA
14 BASHA JAMAL MOHAMMED 41 M 543287 10.2 6.5 3.7
CHOLELITHIASIS WITH
15 KHOTRESH 37 M 678097 8.3 5.2 3.1 D D N D N D D N D N D D N D N A A A P P P P P P NIL B B B
CHOLEDOCHOLITHIASIS
LESION IN LT LOBE OF
HILAR CHOLANGIOCARCINOMA
16 DEVARAJ 65 M 67981 6.7 2.6 4.1 D D N N N D D D N N D D D N N A A A A A A A A A LIVER EXTENDING INTO B M M
(KLATSKIN'S TUMOUR )
PORTA HEPATIS
POLYPOID LESION IN GB
ADENOCARCINOMA OF GB WITH
17 NAGARATHNAMMA 55 F 765059 8.9 5.8 3.1 N N N N N N N N D N N N N D N A A A A A A P P P WITH IMPACTED B B B
CALCULUS CHOLECYSTITIS
CALCULUS
LEVEL OF DUCTAL STATUS IN DUCTAL STATUS IN DUCTAL STATUS IN
BILIRUBIN CALCULI NIGN/MALIGNA
OBSTRUCTION USG CT MRCP
AGE LOCAL EFFECT
S.NO NAME SEX IP NO FINAL DIAGNOSIS
(years) CD CBD GB /METASTASIS
INDIRECT
DIRECT
TOTAL
MRCP
MRCP
MRCP
MRCP
MRCP
IHBD
IHBR
IHBR
CHD
CHD
CHD
USG
USG
CBD
CBD
CBD
USG
USG
USG
PD
PD
PD
CD
CD
CD
CT
CT
CT
CT
CT
MASS HEAD OF
PANCREAS CAUSING CA HEAD OF PANCREAS WITH
18 SANTHAMMA 38 F 7180291 15.9 8.6 7.3 D D N D N D D N D N D D N D+C N A A A A A A A A A IC M M
BILIARY PASSAGE BILIARY OBSTRUCTION
OBSTRUCTION
ABRUPT TERMINATION
OF CBD & MPD AT THE
19 JAGATHAMBAL 50 F 712839 12.9 6.8 6.1 D D N D D D D N D D D D N D+C D A A A A A A A A A M M M CA PANCREAS
LEVEL OF HEAD OF
PANCREAS
CHOLELITHIASIS WITH DISTAL CBD
20 NAZREEN 21 F 712348 10.5 5 5.5 D D N D N D D N D N D D N D+S N A A A A A A P P P NIL B B B
STRICTURE
MASS INVOLVING
POSTERIOR WALL AND
NECK OF GB
21 KAMMALAMMA 63 F 647891 6.7 2.6 4.1 D NV NV N N D D N S N D S S S+N N A A A A A A A A A B M M GB CARCINOMA
EXTENDING INTO
PORTA HEPATIS WITH
METASTASIS
22 ABDUL KATHER 56 M 657791 5.9 2.6 3.3 D NV NV N N D NV N N N D S N N N A A A A A A A A A NIL IC IC M CHOLANGIO CARCINOMA
BENIGN STRICTURE OF DISTAL
23 ANANTHI 36 F 678191 6.1 2.7 3.4 N N NV D N N N NV D N D+B D N S+N N A A A A A A A A A NIL IC IC B
CBD
24 DODAPPA 85 M 7819121 15.6 8.5 7.1 D N N N N D C N C N D C N C N A A A A A A P P P LIVER INVASION B M M GB CARCINOMA
25 MURGESHAPPA 34 M 678923 14.6 6.5 8.1 D NV NV D N D D D D N D D D D N A A A A A A P P P NIL B B B GB CALCULI WITH DISTAL CBD CAL
26 RADHAMMA 72 F 679345 6.8 3 3.8 D D N N N D D N S N D D N S N A P P A A A A A A NIL IC B M PERIAMPULLARY CARCINOMA
27 VENKATESH KUMAR 39 M 774590 11.9 7.9 4 D D N D N D D N D N D D N D N A A A P P P P P P NIL B B B GB STONE WITH CHOLELITHIASIS
28 SHALDA BEGAM 29 F 773245 5.8 2.6 3.2 D D N D N D D N D N D D N D N A A A P P P P P P NIL B B B CHOLEDOCOLITHIASIS
29 RAMAPPA 75 M 774592 18.5 10.9 7.6 D D N N N D D D N N D D D N N A A A A A A P P P RIGHT LOBE LESON B M M CHOLANGIOCARCINOMA
DISTAL CBD
30 SHAKUNTALA 28 F 715690 6.4 2.5 3.9 D D N N N D D N S N D D N S N A A A A A A A A A IC M M PERIAMPULLARY CARCINOMA
OBSTRUCTION
31 KUZHANDAIVEL 53 M 726903 7.3 3.5 3.8 N N NV D N N N NV D N D+B D N S N A A A A A A P P P NIL B B B BENIGN BILIARY STRICTURE
32 RAJENDRAN 51 M 756923 5.3 2.6 2.7 D NV NV D N D D D D N D D D D N A A A P P P P P P NIL B B B CHOLEDOCHOLITHIASIS
LESION IN THE LEFT
33 RAJAKUMARI 57 F 726901 9.5 4.3 5.2 D D N D N D D N D N D D N D+M N A A A A A A A A A B M M CHOLANGIOCARCINOMA
LOBE
COMPRESSION OF
34 RAJESH M 689023 11.9 7.9 4 D D N D N D D N D N D D N D+C N A A A A A A A A A B M M LYMPHOMA
DISTAL CBD
35 B/O SHANTHAMMA 3M M 689134 8.8 11 12 D D NV D N D D D D N D D D D N A A A A A A A A A NIL B B B CHOLEDOCHOCOELE
36 SUBHASH 7 M 729023 15 8.5 7.1 D D NV D N D D D D N D D D D N A A A A A A A A A NIL B B B CAROLI'S DISEASE