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GENERAL DATA
• Q.M
• 55 y.o/female
• Filipino
• Married
• Roman Catholic
• Cordova,Cebu City
• Admitted for the first time in CHH
Chief complaint
• Jaundice
Past Medical History
• Hypertensive for 10 years on maintenance
medication Metoprolol(Neobloc) 100mg OD
• Diabetic (no maintenance medication)
• Nonasthmatic
• No food and drug allergies
• Admitted in 2017 in District hospital due to
Hypokalemia
Family history
• Hypertension on both paternal and maternal
side
• No family history of cancer
History of present illness
• 3 weeks PTA, noted onset of hypogastric pain
,non radiating. No medications taken.
Condition tolerated.
• 1 week PTA, noted onset of icteric sclerae with
persistence of symptoms. Still no consult ws
done.
• 4 days PTA, noted persistence of symptoms
now asssociated with generalized body
weakness
History of Present Illness
• 1 day PTA, sought consult with AP and was
advised for Ultrasound with whole abdomen .
Showed gallstones and was advised to seek
consult with Dr.Bullo for further
manangement.
• Hours PTA, patient sought consult with
dr.Bullo and was requested for CT scan with
contrast whole abdomen thus this admission.
Personal and social habits
• Nonsmoker
• Nonalcoholic
Physical Eaxmination
Seen and examined patient awake, responsive,
afebrile not in respiratory distress, with the
following vital signs:
T: 37.1c BP:100/70 mmHg
P: 57 bpm 02 sat: 95%
R: 20 cpm Wt 69.10
Ht 157.5
BMI 27.86 (overweight)
Physical Examination
• Skin : Jaundice, good turgor and mobility
• HEENT : equal palpebral fissures, icteric
sclerae, pale conjunctivae, symmetric ears, no
deformities, (-) nasoaural discharge , nasal
septum at midline, dry lips, no oral lesions, no
tonsillopharyngeal tonsils,
• Neck : supple , trachea in midline , no
lymphadenopathy
Chest and Lungs: symmetric chest, equal chest
expansion, equal tactile fremitus, clear breath
sound
CVS: Distinct S1 and S2, regular rate and rhythm,
no murmurs
Test result
Alpha-Feto Protein(Liver,Germ 58.8 <7.0
cell tumors)
CA 19-9 (Pancreas, G I T) 139.6 0-37
Admitting impression
• T/C Cholangiocarcinoma
Plan
• Cefuroxime 750 mg IVTT q 8 hr
• CT scan whole abdomen with contrast on
Monday
Cholangiocarcinoma
• Rare tumor arising from biliary epithelium and
may occur anywhere along biliary tree
• 2/3 are located at hepatic duct bifurcation
• Male to female 1.3 : 1
• Common to most risk factors include biliary
stasis, bile duct stones , and infection
• 95 % of bile duct cancers are adenocarcinoma
• Devided into distal ,proximal , or perihilar
tumors
• 2/3 are located perihilar location
• Referred to as Klatsin tumors classigied based
on anatomic location by the Bismuth-Corlette
classification
Type