Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1976
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1978 1
1987 2
1989 5
1990 3
1991 2
1992 2
1993 1
1994 10
1995 3
1996 4
1997 1
1998 5
1999 9
2000 6
2001 6
2002 4
2003 5
2004 5
2005 9
2006 6
2007 4
2008 2
2009 5
2010 4
2011 7
2012 4
2013 8
2014 7
2015 9
2016 5
2017 5
2018 12
2019 5
2020 8
2021 14
2022 7
2023 4
2024 3
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

178 results

Results by year

Filters applied: . Clear all
Page 1
DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma.
González IA, Stewart DR, Schultz KAP, Field AP, Hill DA, Dehner LP. González IA, et al. Mod Pathol. 2022 Jan;35(1):4-22. doi: 10.1038/s41379-021-00905-8. Epub 2021 Oct 1. Mod Pathol. 2022. PMID: 34599283 Free PMC article. Review.
The detection of the germline mutation in DICER1 provided the opportunity to identify and continue to recognize a number seemingly unrelated extrapulmonary neoplasms: Sertoli-Leydig cell tumor, gynandroblastoma, embryonal rhabdomyosarcomas of the cervix and other sites, multinodu …
The detection of the germline mutation in DICER1 provided the opportunity to identify and continue to recognize a number seemingly unrelated …
Neonatal Liver Tumors.
Katzenstein HM, Aguado A, Cheek B, Gresh R. Katzenstein HM, et al. Clin Perinatol. 2021 Mar;48(1):83-99. doi: 10.1016/j.clp.2020.11.005. Clin Perinatol. 2021. PMID: 33583509 Review. No abstract available.
Mesenchymal Neoplasms of the Liver.
Papke DJ Jr. Papke DJ Jr. Surg Pathol Clin. 2023 Sep;16(3):609-634. doi: 10.1016/j.path.2023.04.013. Epub 2023 Jun 11. Surg Pathol Clin. 2023. PMID: 37536892 Review.
Mesenchymal neoplasms of the liver can be diagnostically challenging, particularly on core needle biopsies. Here, I discuss recent updates in neoplasms that are specific to the liver (mesenchymal hamartoma, undifferentiated embryonal sarcoma, calcifying neste
Mesenchymal neoplasms of the liver can be diagnostically challenging, particularly on core needle biopsies. Here, I discuss recent up
Cartilage-forming tumors.
Qasem SA, DeYoung BR. Qasem SA, et al. Semin Diagn Pathol. 2014 Jan;31(1):10-20. doi: 10.1053/j.semdp.2014.01.006. Epub 2014 Jan 23. Semin Diagn Pathol. 2014. PMID: 24680178 Review.
Some of these tumors are true neoplasms while others are hamartomas or developmental abnormalities. The morphologic heterogeneity of these tumors may be explained by a common multipotent mesenchymal cell differentiating along the lines of fetal-adult cartilage matur …
Some of these tumors are true neoplasms while others are hamartomas or developmental abnormalities. The morphologic heterogeneity of …
Malignant liver tumors.
Suriawinata AA, Thung SN. Suriawinata AA, et al. Clin Liver Dis. 2002 May;6(2):527-54, ix. doi: 10.1016/s1089-3261(02)00005-3. Clin Liver Dis. 2002. PMID: 12122869 Review.
Primary malignant liver tumors can arise from different components of the liver, such as hepatocytes, bile duct epithelium, neuroendocrine cells, and mesenchymal cells. A specific diagnosis frequently can be suggested from imaging studies, but biopsy remains the gold stand …
Primary malignant liver tumors can arise from different components of the liver, such as hepatocytes, bile duct epithelium, neuroendocrine c …
Mesenchymal hamartoma of the liver--a case report and literature review.
Rosado E, Cabral P, Campo M, Tavares A. Rosado E, et al. J Radiol Case Rep. 2013 May 1;7(5):35-43. doi: 10.3941/jrcr.v7i5.1334. Print 2013 May. J Radiol Case Rep. 2013. PMID: 23705055 Free PMC article. Review.
We report a case of a mesenchymal hamartoma of the liver in a two-year-old boy. He presented to the emergency room with abdominal distention and vomiting. ...The lesion was surgically resected. Pathological examination revealed a mesenchymal hamartoma
We report a case of a mesenchymal hamartoma of the liver in a two-year-old boy. He presented to the emergency room with abdomi …
Prenatal chest wall mesenchymal hamartoma: a case report and review of the literature.
Sheidaei S, Ghasemi M, Mousavi SA. Sheidaei S, et al. J Matern Fetal Neonatal Med. 2022 Feb;35(3):613-615. doi: 10.1080/14767058.2020.1728737. Epub 2020 Feb 25. J Matern Fetal Neonatal Med. 2022. PMID: 32098529 Review.
Mesenchymal hamartoma of the chest wall (MHCW) is a rare but benign tumor of childhood. Its clinical presentation varies from nonsymptomatic to respiratory distress. ...
Mesenchymal hamartoma of the chest wall (MHCW) is a rare but benign tumor of childhood. Its clinical presentation varies from
A Rare Case of Cardiac Mesenchymal Hamartoma and Comprehensive Review of the Literature With Emphasis on Histopathology.
Jobbagy S, Patel S, Marboe C, Jiang JG, Jobbagy Z. Jobbagy S, et al. Int J Surg Pathol. 2021 Oct;29(7):764-769. doi: 10.1177/10668969211002264. Epub 2021 Mar 22. Int J Surg Pathol. 2021. PMID: 33749361 Review.
This characterization is most consistent with cardiac mesenchymal hamartoma. Relevant differential diagnoses for this lesion include hamartoma of mature cardiac myocytes (HMCMs) and intramuscular hemangioma. ...Absence of S100-positive nerve and mature adipos …
This characterization is most consistent with cardiac mesenchymal hamartoma. Relevant differential diagnoses for this lesion i …
Mesenchymal cystic hamartoma presenting with pneumothorax: case report and review of the literature.
Leopizzi M, Cerbelli B, Merenda E, Pignataro MG, Bassi M, Venuta F, d'Amati G, Della Rocca C, Pernazza A. Leopizzi M, et al. Gen Thorac Cardiovasc Surg. 2020 Dec;68(12):1573-1578. doi: 10.1007/s11748-020-01370-x. Epub 2020 May 2. Gen Thorac Cardiovasc Surg. 2020. PMID: 32361809 Review.
Mesenchymal cystic hamartoma (MCH) of the lung is a rare disease, with an indolent course in the majority of cases. It can be single or multifocal and it is composed of primitive mesenchymal cells admixed with cystic spaces. Only few cases have been reported
Mesenchymal cystic hamartoma (MCH) of the lung is a rare disease, with an indolent course in the majority of cases. It can be
178 results