2010
DOI: 10.1007/s00296-009-1348-y
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Malignancy in scleroderma patients from south west England: a population-based cohort study

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Cited by 36 publications
(31 citation statements)
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“…Hypotheses have been proposed, which suggest that systemic sclerosis and malignancy manifest as a result of alterations in the immune response or genetic background. In a study by Siau et al (3), the average time between initial diagnosis of systemic sclerosis and malignancy was observed to be seven years (3). …”
Section: Discussionmentioning
confidence: 99%
“…Hypotheses have been proposed, which suggest that systemic sclerosis and malignancy manifest as a result of alterations in the immune response or genetic background. In a study by Siau et al (3), the average time between initial diagnosis of systemic sclerosis and malignancy was observed to be seven years (3). …”
Section: Discussionmentioning
confidence: 99%
“…Large cohort in South West England has found that the prevalence of malignancy is increased in SSc [7]. Up to date it is found out that the concomitant malignancies with SSc are solid organ cancers like lung, breast, stomach, oesophagus, colon, pancreas, larynx, over, thyroid, liver, prostate and blood oriented malignancies including leukaemia, lymphoma, melanomas and non-melanomas.…”
Section: Discussionmentioning
confidence: 99%
“…This concurrence is not resulted from SSc but it is thought to be related with pulmonary Wbrosis. Despite the arguments that cytotoxic treatment may increase possibly the hematologic malignancy risk, a medical study based on oral Cyc proved the contrary [7]. After the discovery of the structure of endogenic PGI2 in 1976 by Vane et al, iloprost has been generated in 1978.…”
Section: Discussionmentioning
confidence: 99%
“…In some cases, systemic sclerosis could even represent a paraneoplastic syndrome (Vettori et al, 2010). In a population-based cohort study from south-west England to determine if patients with scleroderma have an increased risk of malignancy compared with general population, the highest risk among patients affected by scleroderma was found for haematological malignancies, especially for NHL (RR=25.8) (Siau et al, 2010). Another retrospective analysis of 218 Hungarian patients with SSc followed during a period of 12 years showed lymphoma development in three of them (1.38%), all of B cell phenotype, within 2 years after the onset of SSc.…”
Section: Systemic Sclerosismentioning
confidence: 99%