Aplastic Anaemia.
نویسنده
چکیده
منابع مشابه
Epidemiology of acquired aplastic anaemia in Pakistan.
BACKGROUND Acquired aplastic anaemia is a rare disease which results in morbidity and mortality at a young age. This study was carried out to determine the clinical presentation, haematological parameters and association factors of acquired aplastic anaemia in a cohort of Pakistani patients. METHODS This was a cross-sectional study conducted at Haematology Department, Shaikh Zayed Hospital, L...
متن کاملEpidemiology of aplastic anaemia in the state of Sabah, Malaysia.
Aplastic anaemia is a rare disease which is more prevalent in the Far East. In Malaysia, it appears to be unusually common in the state of Sabah. A retrospective analysis of all cases of aplastic anaemia diagnosed between January 1993 and March 1996 was undertaken. The criteria of the International Aplastic Anaemia and Agranulocytosis Study (IAAAS) was used. In this 39 month period, 31 cases we...
متن کاملClinical and chromosome studies in Fanconi's aplastic anaemia.
A pernicious anaemia-like picture of the peripheral blood associated with congenital abnormalities was first described by Fanconi (1927) in three brothers. Since then a similar syndrome has been reported from many parts of the world under the title of Fanconi's aplastic anaemia. Gmyrek and Syllm-Rapoport (1964) have reviewed 152 cases in the literature in considerable detail. Bloom et al. (1966...
متن کاملCytogenetic profile of aplastic anaemia in Indian children
BACKGROUND & OBJECTIVES Aplastic anaemia is a rare haematological disorder characterized by pancytopenia with a hypocellular bone marrow. It may be inherited/genetic or acquired. Acquired aplastic anaemia has been linked to many drugs, chemicals and viruses. Cytogenetic abnormalities have been reported infrequently with acquired aplastic anaemia. Majority of the studies are in adult patients fr...
متن کاملCourse and Prognosis in Aplastic Anaemia.
The diagnosis of aplastic anaemia depends upon the demonstration of hypocellularity of the bone-marrow, and before making the diagnosis it is essential to demonstrate this by appropriate marrow aspiration, bone-biopsy, and special investigations: Even so, this diagnosis includes a number of entities which differ in behaviour and prognosis and are probably due to different fundamental defects. T...
متن کاملGuillain Barré syndrome precipitated by the use of antilymphocyte globulin in the treatment of severe aplastic anaemia.
This report describes the case of a 54 year old woman with very severe aplastic anaemia who was treated with antilymphocyte globulin (ALG) and developed Guillain Barré syndrome (GBS). No antecedent infective aetiology was identified. Although there are numerous reports of autoimmune disease after treatment with ALG in aplastic anaemia, and GBS after immunosuppressive treatment, there are none r...
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ورودعنوان ژورنال:
- The Journal of the Association of Physicians of India
دوره 63 3 Suppl شماره
صفحات -
تاریخ انتشار 2015