Thrombotic Microangiopathic Haemolytic Anaemia
نویسندگان
چکیده
منابع مشابه
Thrombotic microangiopathic haemolytic anaemia.
The syndrome of thrombotic microangiopathic haemolytic anaemia is rare and almost all the cases reported have been in adults. Very few cases occurring in childhood have been reported and the youngest recorded case was 22 months old (Craig and Gitlin, 1957). We report the clinical and pathological details and the response to treatment of a child aged 21 months, who was seen at the Austin Hospita...
متن کاملThrombotic microangiopathic haemolytic anaemia and antiphospholipid antibodies.
OBJECTIVE To analyse the clinical and laboratory features of patients with thrombotic microangiopathic haemolytic anaemia (TMHA) associated with antiphospholipid antibodies (aPL). METHODS A computer assisted (PubMed) search of the literature was performed to identify all cases of TMHA associated with aPL from 1983 to December 2002. RESULTS 46 patients (36 female) with a mean (SD) age at pre...
متن کاملMicroangiopathic haemolytic anaemia.
Correspondence BRITISH 465 Melbourne (Daily Telegraph, 30 June). A plastic tube 4 inches (10 cm.) long is reported to have been used, but I doubt if it will be successful as it has no cilia and no secretion. There is yet time to develop, in Britain a live transplant which, even if eventually rejected, would serve to secure at least one SIR,-Microangiopathic haemolytic anaemia (M.H.A.) has been ...
متن کاملCancer-related microangiopathic haemolytic anaemia.
Donato AA, et al. BMJ Case Rep 2017. doi:10.1136/bcr-2017-223382 Description A 71-year-old woman with widely metastatic breast cancer to liver and bone marrow presented with 2 weeks of fatigue. Examination revealed a severely ill-appearing woman in moderate distress with icterus and jaundice. Laboratory investigations revealed profound anaemia (haemoglobin 5.2 g/dL) with appropriate reticulocyt...
متن کاملMicroangiopathic haemolytic anaemia and systemic vasculitis.
Two cases of systemic vasculitis complicated by microangiopathic haemolytic anaemia (MAHA) are described: this association has not previously been reported. Both patients had atypical presentations of their primary disease, one with parotitis and one with a Guillain-Barré syndrome. Other causes of MAHA were excluded and a possible link with macromolecular von Willebrands factor is speculated upon.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: BMJ
سال: 1952
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.2.4790.897