Cholangiocarcinoma

Cholangiocarcinoma (CCA) is a biliary tract cancer (BTC, see this term) originating in the epithelium of the biliary tree, either intra or extra hepatic.



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Narrow down the case reports



Total: 1131 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(53.2%)
25731231
[Useful device for hepatectomy in patients with a surgical history of bile duct-GI tract anastomosis at the porta hepatis].
Amikura K, Sakamoto H, Takahashi A, Ogura T, Omichi K, Ehara K, Fukuda T, Yatsuoka T, Kawashima Y, Tanaka Y.
Gan To Kagaku Ryoho. 2014;41(12):1497-9.
Vascular dilatation Spherocytosis Cholangitis
Biliary Tract Surgical Procedures Females Hepatectomy Homo sapiens Male
2
(48.0%)
9525019
Postoperative abnormal prothrombinemia in patients with cefoperazone: report of two cases.
Narumi S, Sasaki M, Okudera D, Tann E, Konn M.
Surg Today. 1998;28(2):227-30.
Jaundice Anemia
F2
Cephalosporins Colectomy Females Homo sapiens Liver Male Middle Aged Postoperative Complications
2
(48.0%)
192070
Cholangiocarcinoma associated with biliary cirrhosis due to congenital biliary atresia.
Kulkarni PB, Beatty E Jr.
Am J Dis Child. 1977;131(4):442-4.
Jaundice Anemia
Child Child, Preschool Females Follow-Up Studies Homo sapiens Infant Liver Liver Function Tests
4
(46.9%)
25713810
Fascioliasis simulating an intrahepatic cholangiocarcinoma-Case report with imaging and pathology correlation.
Losada H, Hirsch M, Guzman P, Fonseca F, Hofmann E, Alanis M.
Hepatobiliary Surg Nutr. 2015;4(1):E1-7.
Eosinophilia Fever Hepatomegaly Cholangitis
5
(45.2%)
20459809
(2874571)
Cholangiocarcinoma presenting as hemobilia and recurrent iron-deficiency anemia: a case report.
Ahmad SS, Basheer FT, Idris SF, Hariraj R, Mathialagan R, Douds A.
J Med Case Rep. 2010;4:133.
Iron deficiency anemia Hemobilia
6
(44.2%)
29682369
(5846373)
Intrahepatic Cholangiocarcinoma Masquerading as Acute Fatty Liver of Pregnancy: A Case Report and Review of the Literature.
Qasrawi A, Abughanimeh O, Abu Ghanimeh M, Arora-Elder S, Yousef O, Tamimi T.
Case Reports Hepatol. 2018;2018:6939747.
Proteinuria Leukocytosis Hepatomegaly
6
(44.2%)
10955605
Inflammatory pseudotumor of the liver diagnosed by needle liver biopsy under ultrasonographic tomography guidance.
Nakama T, Hayashi K, Komada N, Ochiai T, Hori T, Shioiri S, Tsubouchi H.
J Gastroenterol. 2000;35(8):641-5.
Fever Leukocytosis Hepatomegaly
CRP
Differential Diagnosis Granuloma, Plasma Cell Homo sapiens Liver Abscess Male Ultrasonography
8
(43.7%)
14673730
Intrahepatic sarcomatoid cholangiocarcinoma.
Kaibori M, Kawaguchi Y, Yokoigawa N, Yanagida H, Takai S, Kwon AH, Uemura Y, Kamiyama Y.
J Gastroenterol. 2003;38(11):1097-101.
Anemia Fever Abdominal pain
VIM
Bile Duct Neoplasms Cholangiocarcinoma Fatal Outcome Females Homo sapiens X-Ray Computed Tomography
9
(43.5%)
20716895
[An effective case of gemcitabine therapy with post-operative peritoneal recurrence of intrahepatic cholangiocarcinoma].
Nakayama A, Takasu K, Ogiwara H, Kubo N, Takeuchi N, Tsujimoto K, Ito N, Maruyama A, Shirozaki T, Inoue K, Fujiwara M, Rokuhara T.
Gan To Kagaku Ryoho. 2010;37(8):1595-8.
Ascites Anemia
Bile Duct Neoplasms Cholangiocarcinoma Combined Modality Therapy Deoxycytidine Homo sapiens Liver Male Middle Aged Peritoneal Neoplasms Remission Induction X-Ray Computed Tomography
9
(43.5%)
1648151
Intrahepatic cholangiocarcinoma in hepatolithiasis: A frequently overlooked disease.
Sheen-Chen SM, Chou FF, Eng HL.
J Surg Oncol. 1991;47(2):131-5.
Weight loss Anemia Abdominal mass
Adenocarcinoma Adult Bile Duct Neoplasms Cholelithiasis Females Homo sapiens Male Middle Aged Retrospective Studies
        

Phenotype(s) retrieved from Orphanet

    Total: 8

HPO ID Term Frequency
HP:0000952 Jaundice Very frequent (99-80%)
HP:0011985 Acholic stools Very frequent (99-80%)
HP:0100574 Biliary tract neoplasm Very frequent (99-80%)
HP:0000989 Pruritus Frequent (79-30%)
HP:0012378 Fatigue Frequent (79-30%)
HP:0001945 Fever Occasional (29-5%)
HP:0002027 Abdominal pain Occasional (29-5%)
HP:0002039 Anorexia Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 152

HPO ID Term # of case reports
HP:0030731 Carcinoma 103
HP:0000952 Jaundice 72
HP:0030151 Cholangitis 53
HP:0001394 Cirrhosis 29
HP:0002664 Neoplasm 27
HP:0002617 Dilatation 22
HP:0002027 Abdominal pain 16
HP:0012115 Hepatitis 11
HP:0025615 Abscess 11
HP:0001028 Hemangioma 10
HP:0001945 Fever 10
HP:0002613 Biliary cirrhosis 9
HP:0100279 Ulcerative colitis 9
HP:0001081 Cholelithiasis 8
HP:0001082 Cholecystitis 8
HP:0100523 Liver abscess 8
HP:0100762 Hemobilia 8
HP:0001733 Pancreatitis 7
HP:0002835 Aspiration 7
HP:0002860 Squamous cell carcinoma 7
HP:0003072 Hypercalcemia 7
HP:0001409 Portal hypertension 6
HP:0003003 Colon cancer 6
HP:0200123 Chronic hepatitis 6
HP:0002861 Melanoma 5
HP:0006725 Pancreatic adenocarcinoma 5
HP:0100806 Sepsis 5
HP:0001395 Hepatic fibrosis 4
HP:0001396 Cholestasis 4
HP:0001541 Ascites 4
HP:0001824 Weight loss 4
HP:0002586 Peritonitis 4
HP:0003002 Breast carcinoma 4
HP:0030242 Portal vein thrombosis 4
HP:0031500 Abdominal mass 4
HP:0031625 Pseudoaneurysm 4
HP:0031864 Bacteremia 4
HP:0000819 Diabetes mellitus 3
HP:0002040 Esophageal varix 3
HP:0002090 Pneumonia 3
HP:0002098 Respiratory distress 3
HP:0003418 Back pain 3
HP:0005214 Intestinal obstruction 3
HP:0006562 Viral hepatitis 3
HP:0010566 Hamartoma 3
HP:0030078 Lung adenocarcinoma 3
HP:0031495 Mucinous neoplasm 3
HP:0100242 Sarcoma 3
HP:0000822 Hypertension 2
HP:0000989 Pruritus 2
HP:0001399 Hepatic failure 2
HP:0001907 Thromboembolism 2
HP:0001943 Hypoglycemia 2
HP:0002204 Pulmonary embolism 2
HP:0002315 Headache 2
HP:0002566 Intestinal malrotation 2
HP:0002571 Achalasia 2
HP:0002578 Gastroparesis 2
HP:0002588 Duodenal ulcer 2
HP:0002612 Congenital hepatic fibrosis 2
HP:0002625 Deep venous thrombosis 2
HP:0002894 Neoplasm of the pancreas 2
HP:0005912 Biliary atresia 2
HP:0006280 Chronic pancreatitis 2
HP:0006560 Biliary hyperplasia 2
HP:0010783 Erythema 2
HP:0025318 Ovarian carcinoma 2
HP:0030430 Neuroma 2
HP:0031207 Hepatic hemangioma 2
HP:0040276 Adenocarcinoma of the colon 2
HP:0100008 Schwannoma 2
HP:0000099 Glomerulonephritis 1
HP:0000112 Nephropathy 1
HP:0000211 Trismus 1
HP:0000529 Progressive visual loss 1
HP:0000651 Diplopia 1
HP:0000718 Aggressive behavior 1
HP:0000726 Dementia 1
HP:0000979 Purpura 1
HP:0001046 Intermittent jaundice 1
HP:0001140 Limbal dermoid 1
HP:0001279 Syncope 1
HP:0001287 Meningitis 1
HP:0001289 Confusion 1
HP:0001297 Stroke 1
HP:0001298 Encephalopathy 1
HP:0001413 Micronodular cirrhosis 1
HP:0001658 Myocardial infarction 1
HP:0001695 Cardiac arrest 1
HP:0001735 Acute pancreatitis 1
HP:0001748 Polysplenia 1
HP:0001891 Iron deficiency anemia 1
HP:0001903 Anemia 1
HP:0001937 Microangiopathic hemolytic anemia 1
HP:0002015 Dysphagia 1
HP:0002018 Nausea 1
HP:0002024 Malabsorption 1
HP:0002105 Hemoptysis 1
HP:0002148 Hypophosphatemia 1
HP:0002367 Visual hallucinations 1
HP:0002527 Falls 1
HP:0002583 Colitis 1
HP:0002595 Ileus 1
HP:0002615 Hypotension 1
HP:0002619 Varicose veins 1
HP:0002638 Superficial thrombophlebitis 1
HP:0002719 Recurrent infections 1
HP:0002840 Lymphadenitis 1
HP:0002878 Respiratory failure 1
HP:0002896 Neoplasm of the liver 1
HP:0003128 Lactic acidosis 1
HP:0003198 Myopathy 1
HP:0003419 Low back pain 1
HP:0003537 Hypouricemia 1
HP:0004418 Thrombophlebitis 1
HP:0004420 Arterial thrombosis 1
HP:0004800 Duodenal diverticula 1
HP:0004936 Venous thrombosis 1
HP:0005200 Retroperitoneal fibrosis 1
HP:0005206 Pancreatic pseudocyst 1
HP:0005575 Hemolytic-uremic syndrome 1
HP:0006515 Interstitial pneumonitis 1
HP:0006580 Portal fibrosis 1
HP:0006946 Recurrent meningitis 1
HP:0011854 Hemoperitoneum 1
HP:0012032 Lipoma 1
HP:0012125 Prostate cancer 1
HP:0012126 Stomach cancer 1
HP:0012315 Histiocytoma 1
HP:0012327 Celiac artery compression 1
HP:0012378 Fatigue 1
HP:0012486 Myelitis 1
HP:0012735 Cough 1
HP:0025343 Lupus anticoagulant 1
HP:0025519 Multiple biliary hamartomas 1
HP:0030169 Gastric varix 1
HP:0031035 Chronic infection 1
HP:0031218 Inappropriate antidiuretic hormone secretion 1
HP:0031258 Delirium 1
HP:0031273 Shock 1
HP:0031274 Hypovolemic shock 1
HP:0031678 Atherosclerotic lesion 1
HP:0040319 Dark urine 1
HP:0100005 Testicular mesothelioma 1
HP:0100027 Recurrent pancreatitis 1
HP:0100570 Carcinoid tumor 1
HP:0100621 Dysgerminoma 1
HP:0100633 Esophagitis 1
HP:0100724 Hypercoagulability 1
HP:0100790 Hernia 1
HP:0100844 Pancreatic fistula 1
HP:0100845 Anaphylactic shock 1


Causative gene(s) retrieved from Orphanet

    Total: 1

Gene Symbol Gene Name Entrez Gene ID
PTPN3 protein tyrosine phosphatase non-receptor type 3 5774