Difference between revisions of "Cholangiocarcinoma"
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*''MUC-1'' is also known as ''[[EMA]]''. | *''MUC-1'' is also known as ''[[EMA]]''. | ||
==Molecular== | |||
*Approx. 10% of the tumors carry a [[IDH-1]] or IDH-2 hotspot mutation.<ref>{{Cite journal | last1 = Wang | first1 = P. | last2 = Dong | first2 = Q. | last3 = Zhang | first3 = C. | last4 = Kuan | first4 = PF. | last5 = Liu | first5 = Y. | last6 = Jeck | first6 = WR. | last7 = Andersen | first7 = JB. | last8 = Jiang | first8 = W. | last9 = Savich | first9 = GL. | title = Mutations in isocitrate dehydrogenase 1 and 2 occur frequently in intrahepatic cholangiocarcinomas and share hypermethylation targets with glioblastomas. | journal = Oncogene | volume = 32 | issue = 25 | pages = 3091-100 | month = Jun | year = 2013 | doi = 10.1038/onc.2012.315 | PMID = 22824796 }}</ref> | |||
*FGFR2 gene fusions have been reported.<ref>{{Cite journal | last1 = Wu | first1 = YM. | last2 = Su | first2 = F. | last3 = Kalyana-Sundaram | first3 = S. | last4 = Khazanov | first4 = N. | last5 = Ateeq | first5 = B. | last6 = Cao | first6 = X. | last7 = Lonigro | first7 = RJ. | last8 = Vats | first8 = P. | last9 = Wang | first9 = R. | title = Identification of targetable FGFR gene fusions in diverse cancers. | journal = Cancer Discov | volume = 3 | issue = 6 | pages = 636-47 | month = Jun | year = 2013 | doi = 10.1158/2159-8290.CD-13-0050 | PMID = 23558953 }}</ref> | |||
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Revision as of 07:48, 20 July 2016
Cholangiocarcinoma | |
---|---|
Diagnosis in short | |
Cholangiocarcinoma. H&E stain. | |
| |
Synonyms | bile duct carcinoma |
| |
LM | atypical cuboidal or columnar mucin producing cohesive cells (carcinoma) - usually gland forming (adenocarcinoma), classically with a dense fibrous (desmoplastic) stroma |
LM DDx | metastatic carcinoma - esp. luminal GI tract, hepatocellular carcinoma |
IHC | CK7 +ve, CK20 +ve/-ve, CK19 +ve, HepPar-1 -ve, AFP -ve, EMA +ve |
Site | bile ducts (including pancreas, liver - see liver neoplasms) |
| |
Associated Dx | liver flukes (Clonorchis sinensis, Opisthorchis viverrini), Caroli disease, primary sclerosing cholangitis - esp. in ulcerative colitis |
Signs | +/-jaundice |
Prevalence | uncommon |
Blood work | +/-findings of cholestasis |
Prognosis | poor |
Clin. DDx | other liver tumours - hepatocellular carcinoma, metastases |
Treatment | surgical resection if possible |
Cholangiocarcinoma is a malignant tumour that arise from the bile ducts and may been seen in the liver.
It is also known as bile duct carcinoma.[1]
General
- Malignancy of the biliary tree.
- May be intrahepatic, i.e. intrahepatic cholangiocarcinoma (abbreviated ICC), or extrahepatic.
Epidemiology
- Rare - approximately 1/5 the incidence of HCC.[2]
- More common among asians.
Risks:
- Infection - liver flukes (endemic to Southeast Asia):
- Caroli disease - rare congenital disease.[6]
- Primary sclerosing cholangitis - may be assoc. with inflammatory bowel disease (IBD), esp. ulcerative colitis (UC).
Gross
- Classically one large mass - outline described as cauliflower-like.[7]
- May have satellite nodules.
Image
Microscopic
Features:[8]
- Usually an adenocarcinoma, i.e. gland forming with:
- Cuboidal or columnar mucin producing cells, and
- A dense fibrous (desmoplastic) stroma.
Notes:
- Biliary stents lead to reactive changes,[9] these can be confused for malignancy. One must always check whether a biliary stent was in situ at time of biopsy.[10]
- Usually abundant desmoplasia, ergo hard to get good, i.e. diagnositic, endoluminal brushing specimens.[11]
- May have hyaline inclusions.[12]
DDx:
- Metastatic adenocarcinoma.
- Fulminant hepatic necrosis.
- Bile ducts usu. left behind... look like well-differentiated adenocarcinoma.
- Bile duct adenoma.
- No necrosis, no mitotic activity, no significant nuclear pleomorphism.
Images
Cholangiocarcinoma - low mag. Shows the typical desmoplastic stroma. (WC/Nephron)
www:
- Cholangiocarcinoma & liver flukes - several images (upmc.edu).
- Cholangiocarcinoma - several images (upmc.edu).
IHC
Classic IHC pattern:[13]
ICC vs. HCC:[14]
HCC vs. ICC:[15]
- TTF-1: ~90-100% +ve (cytoplasmic) in HCC vs. ~10% in cholangiocarcinoma.
Note:
- MUC-1 is also known as EMA.
Molecular
- Approx. 10% of the tumors carry a IDH-1 or IDH-2 hotspot mutation.[16]
- FGFR2 gene fusions have been reported.[17]
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MASS, PANCREAS, CORE BIOPSY: - ADENOCARCINOMA, MODERATELY DIFFERENTIATED.
Note:
- On biopsy, it isn't possible to cleanly separate from pancreatic adenocarcinoma. Thus, it is better to stay vague.
Micro
The sections show an atypical gland-forming lesion (adenocarcinoma) in a fibrous background. This lesion is separate from the benign pancreatic glands that are present. The atypical glands are unequally spaced. Moderate-to-marked cytologic atypia is present. Mitotic activity is not readily apparent.
See also
References
- ↑ URL: http://www.cancer.org/cancer/bileductcancer/detailedguide/bile-duct-cancer-what-is-bile-duct-cancer. Access on: 23 May 2013.
- ↑ Iacobuzio-Donahue, Christine A.; Montgomery, Elizabeth A. (2005). Gastrointestinal and Liver Pathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 608. ISBN 978-0443066573.
- ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 926. ISBN 0-7216-0187-1.
- ↑ Park, do H.; Son, HY. (Apr 2008). "Images in clinical medicine. Clonorchis sinensis.". N Engl J Med 358 (16): e18. doi:10.1056/NEJMicm054461. PMID 18420495.
- ↑ de Martel C, Plummer M, Franceschi S (March 2010). "Cholangiocarcinoma: Descriptive epidemiology and risk factors". Gastroenterol Clin Biol. doi:10.1016/j.gcb.2010.01.008. PMID 20202771.
- ↑ Ananthakrishnan AN, Saeian K (April 2007). "Caroli's disease: identification and treatment strategy". Curr Gastroenterol Rep 9 (2): 151–5. PMID 17418061.
- ↑ Nakanishi, Y.; Zen, Y.; Kawakami, H.; Kubota, K.; Itoh, T.; Hirano, S.; Tanaka, E.; Nakanuma, Y. et al. (Jul 2008). "Extrahepatic bile duct carcinoma with extensive intraepithelial spread: a clinicopathological study of 21 cases.". Mod Pathol 21 (7): 807-16. doi:10.1038/modpathol.2008.65. PMID 18425077.
- ↑ Iacobuzio-Donahue, Christine A.; Montgomery, Elizabeth A. (2005). Gastrointestinal and Liver Pathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 609. ISBN 978-0443066573.
- ↑ Carrasco, CH; Wallace, S; Charnsangavej, C; Richli, W; Wright, KC; Fanning, T; Gianturco, C (Dec 1985). "Expandable biliary endoprosthesis: an experimental study.". AJR Am J Roentgenol 145 (6): 1279-81. PMID 3877438.
- ↑ STC. 2 October 2009.
- ↑ 11.0 11.1 STC. 6 December 2010.
- ↑ Aishima, S.; Fujita, N.; Mano, Y.; Iguchi, T.; Taketomi, A.; Maehara, Y.; Oda, Y.; Tsuneyoshi, M. (Sep 2010). "p62+ Hyaline inclusions in intrahepatic cholangiocarcinoma associated with viral hepatitis or alcoholic liver disease.". Am J Clin Pathol 134 (3): 457-65. doi:10.1309/AJCP53YVVJCNDZIR. PMID 20716803.
- ↑ Iacobuzio-Donahue, Christine A.; Montgomery, Elizabeth A. (2005). Gastrointestinal and Liver Pathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 609. ISBN 978-0443066573.
- ↑ [Evaluation of immunohistochemical markers for differential diagnosis of hepatocellular carcinoma from intrahepatic cholangiocarcinoma] Dong H, Cong WL, Zhu ZZ, Wang B, Xian ZH, Yu H. Zhonghua Zhong Liu Za Zhi. 2008 Sep;30(9):702-5. Chinese. PMID 19173916.
- ↑ Lei JY, Bourne PA, diSant'Agnese PA, Huang J (April 2006). "Cytoplasmic staining of TTF-1 in the differential diagnosis of hepatocellular carcinoma vs cholangiocarcinoma and metastatic carcinoma of the liver". Am. J. Clin. Pathol. 125 (4): 519–25. doi:10.1309/59TN-EFAL-UL5W-J94M. PMID 16627262.
- ↑ Wang, P.; Dong, Q.; Zhang, C.; Kuan, PF.; Liu, Y.; Jeck, WR.; Andersen, JB.; Jiang, W. et al. (Jun 2013). "Mutations in isocitrate dehydrogenase 1 and 2 occur frequently in intrahepatic cholangiocarcinomas and share hypermethylation targets with glioblastomas.". Oncogene 32 (25): 3091-100. doi:10.1038/onc.2012.315. PMID 22824796.
- ↑ Wu, YM.; Su, F.; Kalyana-Sundaram, S.; Khazanov, N.; Ateeq, B.; Cao, X.; Lonigro, RJ.; Vats, P. et al. (Jun 2013). "Identification of targetable FGFR gene fusions in diverse cancers.". Cancer Discov 3 (6): 636-47. doi:10.1158/2159-8290.CD-13-0050. PMID 23558953.