Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2009:2009:628206.
doi: 10.1155/2009/628206. Epub 2009 Sep 10.

Malignant rhabdoid tumour of the liver in the young adult: report of first two cases

Affiliations
Case Reports

Malignant rhabdoid tumour of the liver in the young adult: report of first two cases

Ettore Marzano et al. HPB Surg. 2009.

Abstract

Few cases of malignant rhabdoid tumour (MRT) of the liver are reported in literature and always in paediatric patients. We report the first two cases of young adults submitted to hepatic resection for MRT of the liver. A major liver resection was performed in both cases. The histology showed round or fusiform, loosely cohesive cells. The cytoplasm contained abundant eosinophilic inclusions, which caused the nuclei to be located in eccentric locations, giving the characteristic rhabdoid appearance. The immunohistochemical study was performed, and characteristic lack of nuclear INI1 protein expression was found. In a case surgery was associated to chemoradiotherapy. One patient died at 48 months followup for tumour recurrence. The other is still alive at 25 months followup. MRTs are rare tumours of pediatric age with poor prognosis. Hypothetical less malignant behaviour in the young adults could be supposed. Therefore an aggressive surgical and oncological treatment seems justified.

PubMed Disclaimer

Figures

Figure 1
Figure 1
CT-scan (a) and the Magnetic Resonance Imaging (b) showed a voluminous heterogeneous tumour occupying the left liver. The injection of contrast showed a late vascularisation.
Figure 2
Figure 2
The microscopic analysis of the specimen (hemotoxylin, Phloxine, and Safran coloration) with 200 × magnification (a) and 400 × magnification (b).

References

    1. Beckwith JB, Palmer NF. Histopathology and prognosis of Wilms tumor: results from the first national Wilms' Tumor Study. Cancer. 1978;41(5):1937–1948. - PubMed
    1. Weeks DA, Beckwith JB, Mierau GW, Luckey DW. Rhabdoid tumor of kidney: a report of 111 cases from the National Wilms' Tumor Study Pathology Center. American Journal of Surgical Pathology. 1989;13(6):439–458. - PubMed
    1. Gonzalez-Crussi F, Goldschmidt RA, Hsueh W, Trujillo YP. Infantile sarcoma with intracytoplasmic filamentous inclusions. Distinctive tumor of possible histiocytic origin. Cancer. 1982;49(11):2365–2375. - PubMed
    1. Yuri T, Danbara N, Shikata N, et al. Malignant rhabdoid tumor of the liver: case report and literature review. Pathology International. 2004;54(8):623–629. - PubMed
    1. Leong F, Leong A. Malignant rhabdoid tumor in adults-heterogenous tumors with a unique morphological phenotype. Pathology Research and Practice. 1996;192(8):796–807. - PubMed

Publication types