Hepatic cystic hamartoma

Hepatic cystic hamartoma, also named Mesenchyma hamartoma of liver, is a rare benign liver tumor of childhood, usually before the age of 2, of mesenchymal origin and variable clinical presentation (abdominal dissension, abdominal mass, pain, vomiting and signs of inferior vena cava compression).



Input patient's signs and symptoms


Narrow down the case reports



Total: 26 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(31.0%)
21843058
Meckel syndrome with Caroli disease and choledochal cysts.
Venkatachala S, Sivaraman A.
Fetal Pediatr Pathol. 2011;30(5):350-4.
Congenital hepatic fibrosis Polydactyly
Adult Bile Duct Diseases Caroli Disease Choledochal Cyst Ciliary Motility Disorders Females Fetus Homo sapiens Polycystic Kidney Diseases Pregnancy Retinitis Pigmentosa
2
(4.0%)
28485658
Multicystic biliary hamartoma with extremely elevated CA19-9: a case report.
Morinaga T, Imai K, Yamashita YI, Yamao T, Kaida T, Nakagawa S, Hashimoto D, Chikamoto A, Sumiyoshi S, Mikami Y, Baba H.
Scand J Gastroenterol. 2017;52(8):916-919.
Neoplasm
Bile Duct Diseases Bile Duct Neoplasms CA-19-9 Antigen Cyst Differential Diagnosis Endoscopic Retrograde Cholangiopancreatography Hamartoma Hepatectomy Homo sapiens Magnetic Resonance Imaging Male Middle Aged X-Ray Computed Tomography
2
(4.0%)
27956812
(5124993)
Pediatric living donor liver transplantation for congenital hepatic fibrosis using a mother's graft with von Meyenburg complex: A case report.
Yamada N, Sanada Y, Katano T, Tashiro M, Hirata Y, Okada N, Ihara Y, Miki A, Sasanuma H, Urahashi T, Sakuma Y, Mizuta K.
World J Gastroenterol. 2016;22(44):9865-9870.
Congenital hepatic fibrosis
Bile Duct Diseases Biopsy Child Donor Selection Females Genetic Diseases, Inborn Graft Survival Hamartoma Homo sapiens Liver Cirrhosis Liver Function Tests Living Donors Magnetic Resonance Imaging Predictive Value of Tests Time Factors X-Ray Computed Tomography
2
(4.0%)
26017582
A variant of multicystic biliary hamartoma presenting as an intrahepatic cystic neoplasm.
Tominaga T, Abo T, Kinoshita N, Murakami T, Sato Y, Nakanuma Y, Harada K, Masuda J, Nagayasu T, Nanashima A.
Clin J Gastroenterol. 2015;8(3):162-6.
Neoplasm
Adult Bile Duct Diseases Bile Duct Neoplasms Differential Diagnosis Hamartoma Hepatectomy Homo sapiens Male
2
(4.0%)
25328340
(4196361)
Adult hepatic mesenchymal hamartoma: an unusual case.
Sharma M, Bansal P, Goyal NK.
J Lab Physicians. 2014;6(2):124-6.
Hamartoma
2
(4.0%)
24783100
Benign Hepatic Mesenchymal Hamartoma (HMH) - A Case Report.
Patel SR, Misra V, Verma K, Gupta P, Dhingra V.
J Clin Diagn Res. 2014;8(3):119-20.
Hamartoma
2
(4.0%)
24027729
(3762050)
Neonatal mesenchymal hamartoma of liver: an unusual presentation.
Ramareddy RS, Alladi A.
J Clin Neonatol. 2012;1(4):211-3.
Hamartoma
2
(4.0%)
23351454
[Left lobe mesenchymal hamartoma of liver. Uncommon location].
Martinez-Mier G, Canas-Acar J, Gomez-Dorantes S, Santos-Aguilar U, Alderete-Vazquez G, Franco-Ahumada GE.
Cir Cir. 2012;80(5):466-9.
Abdominal pain
Abdominal Pain Biomarkers, Tumor Child, Preschool Epithelial Cells Hamartoma Hepatectomy Homo sapiens Male Mesoderm Neutrophil Infiltration Stromal Cells X-Ray Computed Tomography
2
(4.0%)
23301651
Incidentally discovered white subcupsular liver nodules during laparoscopic surgery: biliary hamartoma and peribiliary gland hamartoma.
Ioannidis O, Iordanidis F, Paraskevas G, Ntoumpara M, Tsigkriki L, Chatzopoulos S, Kotronis A, Papadimitriou N, Konstantara A, Makrantonakis A, Sakkas A, Kakoutis E.
Klin Onkol. 2012;25(6):468-70.
Bile duct proliferation
Adult Bile Duct Diseases Cholecystectomy, Laparoscopic Females Hamartoma Homo sapiens Incidental Findings Male Middle Aged
2
(4.0%)
22567520
(3335557)
Prenatal diagnosis of congenital mesenchymal hamartoma of liver: a case report.
Kodandapani S, Pai MV, Kumar V, Pai KV.
Case Rep Obstet Gynecol. 2011;2011:932583.
Hamartoma
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 8

HPO ID Term # of case reports
HP:0002664 Neoplasm 2
HP:0010566 Hamartoma 2
HP:0001081 Cholelithiasis 1
HP:0001394 Cirrhosis 1
HP:0002612 Congenital hepatic fibrosis 1
HP:0030731 Carcinoma 1
HP:0100242 Sarcoma 1
HP:0100632 Pulmonary sequestration 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID