Case Report On A Case of Cholangiocarcinoma
Case Report On A Case of Cholangiocarcinoma
CASE PRESENTATION
Name: B.F
Age: 72
Sex: Female
Address: Davao City
Informant: Patient
Reliability: 85%
Date of admission: June 13, 2023
CHIEF COMPLAINT
JAUNDICE
HISTORY OF PRESENT ILLNESS
Approximately 34 days PTA, patient noted bipedal edema. No other recalled associated
symptoms such as exertional dyspnea, orthopnea and oliguria.No meds taken, no consult
was done.
Approximately 31 days PTA, now associated with icterisia by neighbour, still with persistence
of bipedal edema. No fever, no abdominal pain, no vomiting, no dysuria, no oliguria, no
dyspnea, no orthopnea, no exertional dyspnea, no chest pain and palpitations.
sought consult with previous AP due to progression of jaundice, advised work-up and
imaging but did not comply due financial constraints.
HISTORY OF PRESENT ILLNESS
In the interim patient would gradually note progression of jaundice, with increasing severity
in her icterisia. This was not associated with dark colored urine, no acholic stools noted.
Patient noted LBM and her neighbours suggested Loperamide 2 tabs OD, and Dicycloverine
OD for 5 days with relief of loose stool. No changes in stool caliber was noted during this
time.
HISTORY OF PRESENT ILLNESS
19 days PTA, sought consult with previous AP due to progression of jaundice and but noted
constipation, again advised work-up and imaging but did not comply due financial
constraints. She was prescribed w/ the following medications:
Pantoprazole 40mg tab
Essentiale Forte 300mg cap
Lactulose Syrup
Patient took the above medications but still with no relief of constipation.
HISTORY OF PRESENT ILLNESS
In the interim above symptoms progressed now associated with body malaise, decreasing
appetite and early satiety patient was noted. Patient would also have occasional episodes of
vague hypogastric discomfort, non migrating in character, PS of 6-8/10 relieved by food
intake.
Due to persistence of above symptoms patient sought consult at the OPD, work up was done
and was noted with the following findings:
CBC - Hepatitis C virus (anti-HCV) - non
● Hgb : 114 reactive
● Hct : 0.34 - Hepatitis B surface antigen (HBsAG)
● RBC : 3.49 QUANTITATIVE - non reactive
● WBC : 6.8
● N : 88 - Sodium - 130 mmol/L
● L :8 - Potassium - 2.80
● M. : 0.11 - Ast - 205 (x6)
● E : 0.01 - Alt - 101 (x1.8)
● B :0 - Albumin - 30
● Plt : 310 - Alkaline phosphatase - 626 (x4.9)
● MCV : 98 - Total bilirubin - 270 (x12)
● MCH : 33 - Direct bilirubin - 241 (x48)
● MCHC : 33 - Indirect bilirubin - 29 (x1.5)
HISTORY OF PRESENT ILLNESS
Patient was then advised admission for further work-up and management hence this case.
PAST MEDICAL HISTORY
No HPN
No DM
No known allergies
(-) CVA
(-) MI
(-) BA
(-) Previous history of PTB
FAMILY HISTORY
GENERAL : (-) fever, (-) anorexia, (-) chills, (+) undocumented weight loss
GASTROINTESTINAL : (-) nausea, (-) vomiting, (+) flatus, (+) loss of appetite
PERIPHERAL VASCULAR : (-) calf tenderness, (+) on and off bipedal edema
MUSCULOSKELETAL : (-) joint pains, (-) aching muscles, (-) extremities weakness
NEUROLOGIC : (-) seizures, (-) memory loss, (-) changes in behavior, personality, sensory
deficits
Vital Signs
● BP : 110/70 mmHg
● HR : 79 bpm
● RR : 21 cpm
● Temp : 36.6 C
● O2 sat : 95% at room air
Anthropometrics
● Weight : 38 kg
● Height : 152 cm
● BMI : 16.4 (Underweight; WHO Guidelines)
PHYSICAL EXAMINATION
Head:
I: symmetrical, (-) alopecia
P: (-) tenderness, (-) masses, (-) areas of tenderness
Ear:
I: (-) discharges, (-) skin tags
P: (-) tenderness tug test, (-) preauricular LA
PHYSICAL EXAMINATION
Neck:
I: (-) tracheal deviation, (-) Jugular vein distention
P: (-) No neck masses
PHYSICAL EXAMINATION
Cardiac Examination:
I: Adynamic precordium
P: no heaves or thrills
A: Regular cardiac rate and rhythm, Distinct S1 and S2 heart sounds, no murmurs
PHYSICAL EXAMINATION
Abdominal Examination:
I: Globular, slightly distended abdomen
A: Normoactive bowel sounds (20’s)
P: Tympanitic on percussion on all quadrants, (+) dullness heard at approx. 10 cm from the
midsternal line.
P: (+) direct tenderness in the lower abdomen.
Extremities
Full pulses, (+) bipedal edema pitting grade 1, CRT less than 2 seconds
DRE: No Gross Lesions, no external masses, w/ good sphincter tone, no internal masses
palpated (+) light yellow stool on examining finger
PHYSICAL EXAMINATION
Neuro
GCS 15
Neurologic
GCS 15
CN I - not assessed
CN II - no visual field loss, PERRLA
CN III, IV, VI - no preferential gaze
CN V - (+) corneal reflex
CN VII - no facial asymmetry
CN VIII - intact hearing
CNIX, X - intact gag reflex
CN XI - (-) shoulder lag, right
CN XII - no tongue deviation
ADMITTING IMPRESSION
VAGUE HYPOGASTRIC
EARLY SATIETY BIPEDAL EDEMA PAIN
Choledocholithiasis
● Creatinine : 40.1
● EGFR : 102
PT 27.3 vs 12.3
INR 2.35
APTT 39.4 vs 29
PTPA 29.4%
IMAGING
CXR
A- PA view, good inspiratory effort
B- no bone deformities, no fractures
C- no double density sign, no cardiomegaly
D- no pneumoperitoneum, sharp
costophrenic angles
E- F- no NGT, ET tubes, clear lung fields, no
foreign objects
IMPRESSION: ATHEROSCLEROTIC
AORTA
ECG INTERPRETATION
Rate 71 bpm
Rhythm-sinus rhythm
Pr interval-0.16 normal
Axis-normal axis
Qrs complex-0.08 normal
T wave-positive deflection
QT interval-0.4 sec
OFFICIAL IMPRESSION:
GENERAL PLANS
● 1L pnss at 90cc/hr
● SD: KCl Drip: 20 meqs + 100 cc PNSS at 10 cc/hr
● NPO for now then CBG q4 while on NPO
● VS q 4
● I and O q shift
PLANS AT THE ER
Jaundice:
- Cannot totally rule out hepatic cause vs Gall bladder etiology hence for ultrasound of WAB
- Will Rule out Hepatitis
T/c Cirrhosis:
- vitamin K supplementation
- Hepatek once diet is resume
- to Start Aminoleban 500 mg IV OD to run for 5 hours
- continue lactulose 30 cc ODHS
PLANS AT THE ER
Hypoalbuminemia:
- Once Diet is resumed plan to start supplemental milk feeding plus beneprotein, to include egg
whites per meal
MEDICATIONS
Given throughout the course of admission
OBJECTIVE FINDINGS
1. Icteric sclera
2. Jaundiced skin
3. Moist lips and oral mucosa, no alar flaring, no ear discharge, no erythematous or
enlarged tonsils
4. Equal chest expansion, no retractions, clear breath sounds
5. Adynamic precordium, no heaves or thrills, no murmurs, normal rate and regular
rhythm.
6. Soft, flabby, non-tender abdomen. Normoactive bowel sounds.
7. Warm, full pulses, mild bipedal edema
8. GCS 15
VS
BP - 11/80
T - 36.7
HR - 76
RR - 22
02 - 97% at room air
ASSESSMENT
Obstructive jaundice secondary to T/C non-alcoholic liver disease Vs liver cirrhosis. R/O
Choledocholithiasis
PLAN
Official impression:
1. MINIMAL ASCITES
2. DIFFUSE LIVER PARENCHYMAL DISEASE WITH HETEROGENEOUS SOLID MASS,
INTRADUCTAL BILIARY ECTASIA AND HEPATIC CYST, SEGMENT 3. TRIPHASIC CT
SCAN SUGGESTED FOR FURTHER EVALUATION.
3. SIMPLE CORTICAL RENAL CYST, LEFT
4. SONOGRAPHICALLY NORMAL PANCREAS, SPLEEN, PARA-AORTIC AREAS AND
URINARY BLADDER
LABS
UA - 6/14
Amber, clear.
PH 6.0
Spec. grav 1.030
Glucose and protein - negative
K - 3.83
DAY 2 OF ADMISSION
SUBJECTIVE COMPLAINTS
OBJECTIVE FINDINGS
1. Icteric sclera
2. Jaundiced skin
3. Moist lips and oral mucosa, no alar flaring, no ear discharge, no erythematous or
enlarged tonsils
4. Equal chest expansion, no retractions, clear breath sounds
5. Adynamic precordium, no heaves or thrills, no murmurs, normal rate and regular
rhythm.
6. Soft, flabby, non-tender abdomen. Normoactive bowel sounds.
7. Warm, full pulses, mild bipedal edema
8. GCS 15
VS
BP - 100/70
T - 36.1
HR - 72
RR - 20
02 - 96% at room air
ASSESSMENT
Obstructive jaundice secondary to T/C non-alcoholic liver disease Vs liver cirrhosis. R/O
Choledocholithiasis
PLAN
Positive
DAY 3 OF ADMISSION
SUBJECTIVE COMPLAINTS
OBJECTIVE FINDINGS
1. Icteric sclera
2. Jaundiced skin (chest, abdomen and face)
3. Moist lips and oral mucosa, no alar flaring, no ear discharge, no erythematous or
enlarged tonsils
4. Equal chest expansion, no retractions, clear breath sounds
5. Adynamic precordium, no heaves or thrills, no murmurs, normal rate and regular
rhythm.
6. Soft, flabby, non-tender abdomen. Normoactive bowel sounds.
7. Warm, full pulses, mild bipedal edema
8. GCS 15
VS
BP - 100/70
T - 36.3
HR - 71
RR - 20
02 - 99% at room air
ASSESSMENT
No organism found
DAY 4 OF ADMISSION
SUBJECTIVE COMPLAINTS
OBJECTIVE FINDINGS
1. Icteric sclera
2. Very mild Jaundiced skin (chest, Face)
3. Moist lips and oral mucosa, no alar flaring, no ear discharge, no erythematous or
enlarged tonsils
4. Equal chest expansion, no retractions, clear breath sounds
5. Adynamic precordium, no heaves or thrills, no murmurs, normal rate and regular
rhythm.
6. Soft, flabby, non-tender abdomen. Normoactive bowel sounds.
7. Warm, full pulses, mild bipedal edema
8. GCS 15
VS
BP - 120/80
T - 36.9
HR - 74
RR - 20
02 - 99% at room air
ASSESSMENT
PLAN
Bile duct cancer is a rare disease in which malignant (cancer) cells form in the bile ducts. Bile
duct cancer is also called cholangiocarcinoma. There are two types of cholangiocarcinomas -
1. Intrahepatic cholangiocarcinomas
2. Extrahepatic cholangiocarcinomas
TYPES OF CHOLANGIOCARCINOMAS
Intrahepatic bile duct cancer: This type of cancer forms in the bile ducts inside the liver. Only a small
number of bile duct cancers are intrahepatic. Intrahepatic bile duct cancers are also called intrahepatic
cholangiocarcinomas.
TYPES OF CHOLANGIOCARCINOMAS
Extrahepatic bile duct cancer: This type of cancer forms in the bile ducts outside the liver. The two types of
extrahepatic bile duct cancer are perihilar bile duct cancer and distal bile duct cancer:
1. Perihilar bile duct cancer: This type of cancer is found in the area where the right and left bile ducts
exit the liver and join to form the common hepatic duct. Perihilar bile duct cancer is also called a
Klatskin tumor or perihilar cholangiocarcinoma.
2. Distal bile duct cancer: This type of cancer is found in the area where the ducts from the liver and
gallbladder join to form the common bile duct. The common bile duct passes through the pancreas and
ends in the small intestine. Distal bile duct cancer is also called extrahepatic cholangiocarcinoma.
COMMON PRESENTATION
Stage I: Stage I intrahepatic bile duct cancer is divided into stages IA and IB.
- In stage IB, cancer has formed in an intrahepatic bile duct and the tumor is larger than 5
centimeters.
Intrahepatic bile duct cancer staging
Stage II: In stage II intrahepatic bile duct cancer, either of the following is found:
- the tumor has spread through the wall of an intrahepatic bile duct and into a blood vessel; or
- more than one tumor has formed in the intrahepatic bile duct and may have spread into a
blood vessel.
Intrahepatic bile duct cancer staging
Stage III: Stage III intrahepatic bile duct cancer is divided into stages IIIA and IIIB.
Stage IV: In stage IV intrahepatic bile duct cancer, cancer has spread to other parts of the
body, such as the bone, lungs, distant lymph nodes, or tissue lining the wall of the abdomen
and most organs in the abdomen.
Perihilar bile duct cancer staging
Stage 0:
In stage 0 perihilar bile duct cancer (carcinoma in situ), abnormal cells are found in the
innermost layer of tissue lining the perihilar bile duct. These abnormal cells are not actually
cancer but may become cancer and spread into nearby normal tissue. Stage 0 is also called
high-grade dysplasia.
Stage I: In stage I perihilar bile duct cancer, cancer has formed in the innermost layer
of tissue lining the perihilar bile duct and has spread into the muscle layer or fibrous tissue
layer of the perihilar bile duct wall.
Stage II: In stage II perihilar bile duct cancer, cancer has spread through the wall of
the perihilar bile duct to nearby fatty tissue or to liver tissue.
Perihilar bile duct cancer staging
Stage III: Stage III perihilar bile duct cancer is divided into stages IIIA, IIIB, and IIIC.
Stage IV: Stage IV perihilar bile duct cancer is divided into stages IVA and IVB.
- Stage IVB: Cancer has spread to other parts of the body, such as the liver, lung, bone,
brain, skin, distant lymph nodes, or tissue lining the wall of the abdomen and most organs in
the abdomen
Distal bile duct cancer staging
Stage 0:
Stage I:
In stage I distal bile duct cancer, cancer has formed and spread fewer than 5 millimeters into
the wall of the distal bile duct
Distal bile duct cancer staging
Stage II: Stage II distal bile duct cancer is divided into stages IIA and IIB.
● fewer than 5 millimeters into the wall of the distal bile duct and has spread to 1 to 3
nearby lymph nodes; or
● 5 to 12 millimeters into the wall of the distal bile duct.
- Stage IIB: Cancer has spread 5 millimeters or more into the wall of the distal bile duct.
Cancer may have spread to 1 to 3 nearby lymph nodes
Distal bile duct cancer staging
Stage III: Stage III distal bile duct cancer is divided into stages IIIA and IIIB.
- Stage IIIA: Cancer has spread into the wall of the distal bile duct and to 4 or more
nearby lymph nodes.
- Stage IIIB: Cancer has spread to the large vessels that carry blood to the organs in the
abdomen. Cancer may have spread to 1 or more nearby lymph nodes.
Stage IV: In stage IV distal bile duct cancer, cancer has spread to other parts of the body,
such as the liver, lungs, or tissue lining the wall of the abdomen and most organs in the
abdomen
DIAGNOSTIC MODALITIES
BIOPSY
➔ Laparoscopy:
➔ Endoscopic ultrasound (EUS)
TREATMENT OF CHOLANGIOCARCINOMA
TREATMENT OPTIONS
1. Biliary bi-pass
2. Endoscopic stent placement
3. Percutaneous transhepatic biliary drainage
RADIATION THERAPY
1. External radiotherapy
w/ or w/o hyperthermia therapy or radiosensitizers
2. Internal radiotherapy
CHEMOTHERAPY
1. Systemic chemotherapy
- Gemcitabine and Cisplatin
- Capecitabine and Oxaliplatin (XELOX)
- Gemcitabine and Oxaliplatin (GEMOX)
- Gemcitabine and Capecitabine
2. Internal radiotherapy
TARGETED THERAPY
The following targeted therapies are being studied in patients with bile duct cancer
that is locally advanced and cannot be removed by surgery or has spread to other
parts of the body:
1. ivosidenib
2. pemigatinib
3. infigratinib
IMMUNOTHERAPY
Immune checkpoint inhibitor therapy is a type of immunotherapy. The following
immune checkpoint inhibitor are used to treat bile duct cancer:
1. pembrolizumab
2. durvalumab