Pancoast syndrome and hepatocellular carcinoma – a rare association

Authors

  • Isália Miguel Serviço de Medicina III, Serviço de Anatomia Patológica, do Hospital Distrital de Santarém
  • Helena Vieira Dias Serviço de Medicina III, Serviço de Anatomia Patológica, do Hospital Distrital de Santarém
  • Ana Costa Braga Serviço de Medicina III, Serviço de Anatomia Patológica, do Hospital Distrital de Santarém
  • Christine Dellau Serviço de Medicina III, Serviço de Anatomia Patológica, do Hospital Distrital de Santarém
  • Maria Filomena Roque Serviço de Medicina III, Serviço de Anatomia Patológica, do Hospital Distrital de Santarém

Keywords:

Pancoast´s syndrome, hepatocellular carcinoma, bone metastasis, HCV

Abstract

Pancoast´s syndrome (PS) includes all signs and symptoms resulting from a tumor affecting the pulmonary apex and adjacent
structures. Its main clinical feature is pain in the shoulder, supra-clavicular and arm along with the distribution of the ulnar nerve.
The majority of cases are caused by non-small-cell bronchogenic
carcinoma. Etiologic diagnosis is mostly achieved by histological
examination of a percutaneous transthoracic needle biopsy. PS
is a rare manifestation of a hepatocellular carcinoma (HCC). HCC
is the most common primary liver tumor having a multifactorial
etiology and high mortality rates. It often spreads itself to the lungs
and regional lymphatic nodes; bone metastases are uncommon
(2-20%); Patients with HCC can experience bone pain with no
signs of hepatic dysfunction.

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References

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Additional Files

Published

2013-09-30

How to Cite

1.
Miguel I, Vieira Dias H, Costa Braga A, Dellau C, Roque MF. Pancoast syndrome and hepatocellular carcinoma – a rare association. RPMI [Internet]. 2013 Sep. 30 [cited 2024 Sep. 7];20(3):119-22. Available from: https://revista.spmi.pt/index.php/rpmi/article/view/1086

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Section

Case Reports