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Primary Liver Large B-Cell Lymphoma: A Rare Diagnosis

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DOI: 10.4236/ojbd.2015.51002    4,637 Downloads   5,261 Views  
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Joana de Castro Rocha1, Raquel Lopes2, Ana Rita Cruz1, Cristina Gonçalves2, João Araújo Correia1, Jorge Coutinho2

Affiliation(s)

1Internal Medicine Department, Centro Hospitalar do Porto, Porto, Portugal.
2Hematology Department, Centro Hospitalar do Porto, Porto, Portugal.

ABSTRACT

Primary liver lymphoma is extremely rare, in most of cases it is a B cell lymphoma. Usually the diagnosis is made in middle-aged individuals and most of them have a relatively short life expectancy. In this article, the authors present a case report of a 75-year-old woman with symptoms of three weeks of evolution of diffuse abdominal pain, asthenia and anorexia. The analysis showed cyto cholestasis and the radiological image with lush hepatomegaly because of a large hepatic mass. The patient started chemotherapy and actually is well twenty months after the end of the chemotherapy.

KEYWORDS

Large B Cell Lymphoma, Liver, Rarity

Cite this paper

de Castro Rocha, J. , Lopes, R. , Cruz, A. , Gonçalves, C. , Correia, J. and Coutinho, J. (2015) Primary Liver Large B-Cell Lymphoma: A Rare Diagnosis. Open Journal of Blood Diseases, 5, 9-12. doi: 10.4236/ojbd.2015.51002.

Conflicts of Interest

The authors declare no conflicts of interest.

References

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