Haemolytic uraemic syndrome preceding acute lymphoblastic leukaemia

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Atypical haemolytic uraemic syndrome as a complication of induction chemotherapy for acute lymphoblastic leukaemia.

This report describes a case of fatal haemolytic uraemic syndrome (HUS) developing in a child with acute lymphoblastic leukaemia (ALL) during induction chemotherapy. The aetiology in this case is uncertain but it may have resulted from treatment with L-asparaginase or vincristine. The possibility of HUS during induction chemotherapy for ALL should be considered early on in the treatment regimen...

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CASE REPORT Atypical haemolytic uraemic syndrome as a complication of induction chemotherapy for acute lymphoblastic leukaemia

This report describes a case of fatal haemolytic uraemic syndrome (HUS) developing in a child with acute lymphoblastic leukaemia (ALL) during induction chemotherapy. The aetiology in this case is uncertain but it may have resulted from treatment with L-asparaginase or vincristine. The possibility of HUS during induction chemotherapy for ALL should be considered early on in the treatment regimen...

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Haemolytic uraemic syndrome following acute pancreatitis.

CONTEXT Haemolytic uraemic syndrome is a common cause of renal failure in children but it is a rare condition in adults. Acute pancreatitis in adult as a cause of haemolytic uraemic syndrome is very rare. CASE REPORT A 19-year-old male presented with symptom and signs suggestive of acute pancreatitis which was confirmed as his serum amylase was significantly raised. Within three days of admis...

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Atypical haemolytic uraemic syndrome.

The haemolytic uraemic syndrome (HUS) is characterized by the triad of thrombocytopenia, microangiopathic haemolytic anaemia and acute renal failure. HUS may be classified as either diarrhoeal-associated or non-diarrhoeal/atypical (aHUS). aHUS has recently been shown to be a disease of complement dysregulation, with 50% of cases involving the complement regulatory genes, factor H (CFH), membran...

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Haemolytic uraemic syndrome

Haemolytic uraemic syndrome and the related disorder thrombotic thrombocytopenic purpura have recently been the subject of much interest and research.' A wide variety of phenomena have been observed and several pathogenetic mechanisms have been proposed, matched by a correspondingly diverse array of promising but unsubstantiated methods of treatment. Consideration of the heterogeneity of the cl...

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ژورنال

عنوان ژورنال: Case Reports

سال: 2011

ISSN: 1757-790X

DOI: 10.1136/bcr.05.2011.4285