Intrahepatic cholangiocarcinoma as a rare secondary malignancy after allogeneic hematopoietic stem cell transplantation for childhood acute lymphoblastic leukemia: A case report. (16th January 2020)
- Record Type:
- Journal Article
- Title:
- Intrahepatic cholangiocarcinoma as a rare secondary malignancy after allogeneic hematopoietic stem cell transplantation for childhood acute lymphoblastic leukemia: A case report. (16th January 2020)
- Main Title:
- Intrahepatic cholangiocarcinoma as a rare secondary malignancy after allogeneic hematopoietic stem cell transplantation for childhood acute lymphoblastic leukemia: A case report
- Authors:
- Good, Meghan L.
Malekzadeh, Parisa
Kriley, Isaac R.
Shah, Nirali N.
Kleiner, David E.
Calvo, Katherine
Hernandez, Jonathan M.
Davis, Jeremy L. - Abstract:
- Abstract: Secondary malignancies are a significant cause of non‐relapse mortality in patients who undergo allogeneic HCT. However, secondary liver cancer is rare, and ICC following HCT has never been reported in the literature. Secondary solid cancers typically have a long latency period, and cholangiocarcinoma is classically a malignancy occurring in older individuals. Here, we report the first case of secondary ICC, which presented just 3 years after HCT in a young adult with a history of childhood ALL. A 26‐year‐old male with history of precursor B‐cell ALL presented with asymptomatic elevated liver function tests 3 years after HCT. Laboratories were indicative of biliary obstruction. ERCP showed focal biliary stricturing of the common and left hepatic ducts. MRCP revealed left intrahepatic duct dilatation, suggestive of intrahepatic obstructing mass. Additional workup lead to a clinical diagnosis of ICC. The patient underwent left hepatectomy with extrahepatic bile duct resection and portal lymphadenectomy. Surgical pathology was consistent with moderately differentiated cholangiocarcinoma. Our case illustrates a rare SMN following HCT for ALL. It is the first case report of ICC occurring as a secondary cancer in this patient population. Although cholangiocarcinoma is characteristically diagnosed in the older population, it must remain on the differential for biliary obstruction in post‐HCT patients.
- Is Part Of:
- Pediatric transplantation. Volume 24:Number 2(2020)
- Journal:
- Pediatric transplantation
- Issue:
- Volume 24:Number 2(2020)
- Issue Display:
- Volume 24, Issue 2 (2020)
- Year:
- 2020
- Volume:
- 24
- Issue:
- 2
- Issue Sort Value:
- 2020-0024-0002-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-01-16
- Subjects:
- acute lymphoblastic leukemia -- bone marrow transplant -- case report -- cholangiocarcinoma -- hematopoietic stem cell transplant -- Intrahepatic cholangiocarcinoma -- secondary malignancy
Transplantation of organs, tissues, etc. in children -- Periodicals
617.95408305 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=ptr ↗
http://www.blackwellpublishing.com/journal.asp?ref=1397-3142&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1399-3046 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/petr.13653 ↗
- Languages:
- English
- ISSNs:
- 1397-3142
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.628330
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