Skip to main content
Gut logoLink to Gut
. 1970 May;11(5):423–429. doi: 10.1136/gut.11.5.423

Liver in haemoglobin H disease

Chew Beng Keng, Tan Kheng Khoo
PMCID: PMC1411547  PMID: 5428045

Abstract

There have been no published reports on the liver of patients with haemoglobin H disease. In 11 Chinese patients studied (six male and five female) with haemoglobin H disease hepatic function and histology were studied. Liver function was normal in all cases; however, the gamma globulin level was raised in four cases, the increase being mainly in IgG in all cases and IgA in six cases. Liver histology showed that one case had portal cirrhosis, six cases mild fibrosis, and four cases no fibrosis. Haemosiderosis, mainly in the parenchymal cells of the peripheral lobules, was mild in one case, moderate in four, and severe in the remainder of the cases.

Full text

PDF
423

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BOGOCH A., CASSELMAN W. G., MARGOLIES M. P., BOCKUS H. L. Liver disease in sickle cell anemia; a correlation of clinical, biochemical, histologic and histochemical observations. Am J Med. 1955 Oct;19(4):583–609. doi: 10.1016/0002-9343(55)90348-x. [DOI] [PubMed] [Google Scholar]
  2. BOWDLER A. J., HUEHNSER Thalassaemia minor complicated by excessive iron storage. Br J Haematol. 1963 Jan;9:13–24. doi: 10.1111/j.1365-2141.1963.tb05436.x. [DOI] [PubMed] [Google Scholar]
  3. Bannerman R. M., Keusch G., Kreimer-Birnbaum M., Vance V. K., Vaughan S. Thalassemia intermedia, with iron overload, cardiac failure, diabetes mellitus, hypopituitarism and porphyrinuria. Am J Med. 1967 Mar;42(3):476–486. doi: 10.1016/0002-9343(67)90276-8. [DOI] [PubMed] [Google Scholar]
  4. Berry C. L., Marshall W. C. Iron distribution in the liver of patients with thalassaemia major. Lancet. 1967 May 13;1(7498):1031–1033. doi: 10.1016/s0140-6736(67)91543-7. [DOI] [PubMed] [Google Scholar]
  5. Chew Beng Keng Latex fixation tests in liver diseases. Singapore Med J. 1966 Mar;7(1):38–41. [PubMed] [Google Scholar]
  6. GREEN T. W., CONLEY C. L., BERTHRONG M. [The liver in sickle cell anemia]. Bull Johns Hopkins Hosp. 1953 Feb;92(2):99–127. [PubMed] [Google Scholar]
  7. JIM R. T. Haemoglobin H disease in Hawaii. Acta Haematol. 1962;27:274–277. doi: 10.1159/000206807. [DOI] [PubMed] [Google Scholar]
  8. JORDAN R. A. Cholelithiasis in sickle cell disease. Gastroenterology. 1957 Dec;33(6):952–958. [PubMed] [Google Scholar]
  9. Kent G., Popper H. Liver biopsy in diagnosis of hemochromatosis. Am J Med. 1968 Jun;44(6):837–841. doi: 10.1016/0002-9343(68)90083-1. [DOI] [PubMed] [Google Scholar]
  10. Nanakorn S., Wasi P., Suingdumrong A. Hemoglobin H disease in Thailand. Clinical and hematological studies in 138 cases. Isr J Med Sci. 1965 Jul;1(4):762–764. [PubMed] [Google Scholar]
  11. SONG Y. S. Hepatic lesions in sickle cell anemia. Am J Pathol. 1957 Mar-Apr;33(2):331–351. [PMC free article] [PubMed] [Google Scholar]
  12. VELLA F. Abnormal haemoglobin variants in 10,441 Chinese subjects. Acta Haematol. 1960 Jun;23:393–397. doi: 10.1159/000206259. [DOI] [PubMed] [Google Scholar]

Articles from Gut are provided here courtesy of BMJ Publishing Group

RESOURCES