Skip to main content
Log in

Hepatocellular adenoma: A case with a solitary huge one surgically excised successfully

  • Case Report
  • Published:
Gastroenterologia Japonica Aims and scope Submit manuscript

Summary

A case of hepatocellular adenoma was reported, who showed bleeding tendency, coagulation abnormalities, amenorrhea, hypertention, and albuminuria which all returned to normal negative after successful right hepatic lobectomy. Laboratory data on blood coagulation was suggstive of incrcases of Ac-globulin (Factor V, Proaccelerin) and/or fibrin-stabilizing-factor in the plasma probably released from the adenoma although they were not determined. Hypertention and albuminuria might be induced by downward displacement of the right kidney and stretching of the right renal arterties by a huge tumor, and it is most likely that this adenoma was the cause of these adnomalities: bleeding tendency and also amenorrhea.

Hepatocellular adenoma is a rare tumor of the liver, besides that with some metabolic abnormalities is extremely rare. Hepatomas accompanying some metabolic functions have been already reported as “paraneoplastic syndromes”, but none of such a case as shown here was presented. This case is probably the first one of hepatocellular adenoma with probable increases of Ac-globulin and/or fibrin-stabilizing-factor in the plasma and with some other syndromes which all disappeared after removing the adenoma.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Viallet, A. et al., Primary carcinoma of the liver and dysproteinemia. Gastroenterol. 43; 88, 1962.

    CAS  Google Scholar 

  2. Henson, S.T. et al., Benign tumor of the liver, Surg. Gyne. & Obst., 193; 23, 1956.

    Google Scholar 

  3. Warvi, W.N., Primary tumors of the liver., Surg. Gyne. & Obst., 80; 643, 1954.

    Google Scholar 

  4. Araki, Y., Biochmical syndromes of primary cancer of the liver, Naika, 16; 1048, 1965.

    PubMed  CAS  Google Scholar 

  5. Becker, F., Extremitätennekrose bei Polycythaemia vera., Klin. Wscher., 2; 1260, 1932.

    Article  Google Scholar 

  6. McFadzean, A.J.S. et al, Polycythemia in primary carcinoma of the liver, Blood 13; 427, 1958.

    PubMed  CAS  Google Scholar 

  7. Donati, R.M. et al., Erythrocythemia and neoplastic tumors, Ann. Int. Med., 58; 47, 1963.

    PubMed  CAS  Google Scholar 

  8. Josephs, B. M. et al., Polycythemia secondary to hamartoma of the liver, JAMA 179; 867, 1962.

    PubMed  CAS  Google Scholar 

  9. Feasby, W. R. Primary carcinoma of the liver, Canad. Med. Assoc. J., 53; 486, 1945.

    Google Scholar 

  10. Kwaan, H.C. et al, Antifibrinolytic activity in primary carcinoma of the liver, Clin. Sci., 18; 251, 1959.

    PubMed  CAS  Google Scholar 

  11. Clinico-pathological conference, Am. J. Med., 29; 1060, 1960.

    Google Scholar 

  12. Desbuquois, B. et al., Les tumeurs malignes du foie, p. 129, Masson & Cie, Paris, 1963.

    Google Scholar 

  13. Natsume et al., Wandering kidney and hypertention. J. Jap. Soc. Intern. Med., 53; 1218, 1964.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kurokawa, K., Oda, T., Suzuki, H. et al. Hepatocellular adenoma: A case with a solitary huge one surgically excised successfully. Gastroenterol Jpn 3, 390–395 (1968). https://doi.org/10.1007/BF02782266

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02782266

Keywords

Navigation