COELIAC DISEASE haematological features. and delay in diagnosis
- 1 October 1979
- journal article
- Published by Wiley in The Medical Journal of Australia
- Vol. 2 (7) , 335-338
- https://doi.org/10.5694/j.1326-5377.1979.tb104135.x
Abstract
Seventy patients consecutively diagnosed as having coeliac disease were studied with regard to the clinical and laboratory features of related blood disorders and the delays that occurred in making the eventual correct diagnosis. Eighty-four percent of these patients had some readily demonstrable haematological abnormality. Thrombocytosis was present in 44% of the patients appropriately studied and hyposplenism was diagnosed in 21% of the total group. The importance of associating these conditions with coeliac disease has been stressed. The average delay from the time of initial presentation with relevant symptoms to correct diagnosis was 73 months.Keywords
This publication has 11 references indexed in Scilit:
- Lymphocyte subpopulations in adult coeliac disease.Gut, 1978
- Celiac sprue and refractory sprueGastroenterology, 1978
- Hyposplenism in inflammatory bowel disease.Gut, 1978
- THE CHANGING CLINICAL PRESENTATION OF COELIAC DISEASE IN ADULTSThe Medical Journal of Australia, 1977
- Thrombocytosis in Patients with Celiac SprueGastroenterology, 1976
- Splenic Function in Adult Coeliac DiseaseBritish Journal of Haematology, 1970
- ADULT CŒLIAC DISEASE IN HYPOSPLENIC PATIENTSThe Lancet, 1970
- Malignancy in adult coeliac disease and idiopathic steatorrhoeaThe American Journal of Medicine, 1967
- Lymphoreticular dysfunction in idiopathic steatorrhoea.Gut, 1966
- THREE FATAL ADULT CASES OF MALABSORPTION OF FATArchives of internal medicine (1908), 1923