A Coagulation Defect in Amyloidosis
نویسندگان
چکیده
The association of the presence of an abnormal serum protein fraction between P and y globulins in reticuloendothelial disease and lymphatic leukaemia is a Ml recognized phenomenon (Rundles et al., 1954; Buffa and Rappaport, 1957; Owen e* 1959). The combination of leukaemia and amyloidosis is also recognized, but he presence of a coagulation defect in amyloidosis must be relatively uncommon. CASE HISTORY A man aged 60 was first seen in another hospital in October 1958 with a four week history of Pain in the left hypochondrium and a feeling of fulness in the lower abdomen after meals. We had recently noted a swelling in the left upper quadrant. On examination, the liver and the sPleen were both enlarged, and lymph glands were palpable in both axillae.
منابع مشابه
Acquired Factor X Deficiency Associated with Systematized Amyloidosis - A Report
C OAGULATION DEFECTS due to the lack of a single blood clotting factor are almost exclusively congenital and symptoms appear in early life. Acquired defects other than iatrogenic are usually the result of liver dysfunction and in such cases more than one clotting factor is depressed. A case of selective factor X deficiency developing in middle life and associated with extensive amyloidosis has ...
متن کاملAmyloidosis presenting as severe bleeding diathesis
Bleeding is one of the rare presentations of Amyloidosis. The mechanism behind spontaneous or periinterventional bleeding in patients of amyloidosis is complex and involves multiple co-existing factors like coagulation factor deficiency, abnormal synthesis of coagulation factors due to advanced liver dysfunction, acquired Von Willebrand disease, platelet dysfunction, amyloid angiopathy and othe...
متن کاملRecessive dystrophic epidermolysis bullosa (RDEB) complicated by secondary hepatic amyloidosis
Fig 1. Squamous cell carcinoma identified after multiple biopsy specimens of poorly healing area over left E pidermolysis bullosa (EB) consists of a heterogeneous group of autosomal dominant or recessive disorders, characterized by epithelial fragility. In dystrophic EB, patients have a genetic defect in the gene encoding collagen VII, COL7A1. Generalized severe recessive dystrophic EB (RDEB) i...
متن کاملFactor X deficiency: An uncommon presentation of AL amyloidosis
Factor X deficiency is the most common coagulation factor deficiency amongst patients with AL amyloidosis. It presumably occurs due to adsorption of factor X to amyloid fibrils. The deficiency of this factor, in conjunction with other hemostatic defects, can cause bleeding complications. A case of acquired factor X deficiency due to AL amyloidosis is reported, where abnormal coagulation paramet...
متن کاملSELF ASSESSMENT ANSWERS Purple skin and a swollen thigh in an alcoholic
Q1: How would you describe these skin lesions? What is the differential diagnoses? Figure 1 (see p 430) shows confluent ecchymosis in the background of icteric skin, mainly involving the left thigh. The differential diagnoses of non-palpable purpura/ ecchymosis include primary skin conditions (trauma, solar purpura, steroid purpura, capillaritis, and lividoid vasculitis), clotting disorders (th...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 76 شماره
صفحات -
تاریخ انتشار 1961