Haemolytic anaemia in Indian childhood cirrhosis.

نویسندگان

  • A Perkash
  • A Nair
  • R Bhorchi
  • B N Walia
چکیده

Perkash, A., Nair, A., Bhorchi, R., and Walia, B. N. S. (1971). Archives of Disease in Childhood, 46, 45. Haemolytic anaemia in Indian childhood cirrhosis. Fifty-five patients with Indian childhood cirrhosis were investigated for the occurrence of haemolysis and for its possible underlying mechanisms. Increased haemolysis was present in 76°/o of patients, and was severe in 12%. The degree of anaemia was not always proportional to the severity of haemolysis. No single factor accounted for haemolysis. Evidence of hypersplenism was present in only 7 (13%) patients. The haemolysis appeared to be more severe in patients with advanced liver disease. Evidence for autoimmune haemolytic anaemia was found in 27% of patients. No relation was seen between the degree of haemolysis and hypercholesterolaemia. These findings are compared with those reported in adult patients with cirrhosis of the liver.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Indian Childhood Cirrhosis: Case Report and Pediatric Diagnostic Challenges

Introduction: Indian childhood cirrhosis is a chronic liver disease usually seen in paediatric age group and is unique to the Indian subcontinent. The definitive causative factor for the disease is not found till now but excess copper ingestion has been associated with it.Case presentation: An Indian origin one and half year old premorbidly normal male child presented with history of gradual di...

متن کامل

Atypical congenital haemolytic anaemia.

The most common type of congenital haemolytic anaemia found in Great Britain is familial haemolytic anaemia (chronic acholuric jaundice). A similar congenital haemolytic anaemia may be found on rare occasions in children in whom the red cells do not show spherocytosis, or increased osmotic fragility. The response to splenectomy is not very satisfactory and the syndrome does not fit into the est...

متن کامل

Decrease of serum cholesterol ester in haemolytic disease of the newborn.

The conception of the pathological entity of the three manifestations of haemolytic disease of the newborn: hydrops foetalis, icterus gravis and congenital haemolytic anaemia has been confirmed by the discovery of the Rhesus factor. Moreover, this discovery has allowed us finally to abandon any sharp clinical distinction between the two latter forms of the disease. This is in accord with the fa...

متن کامل

Haemolytic anaemia in a child receiving nitrofurantoin.

In 1956, West and Zimmerman reported a 'first case' of haemolytic anaemia, apparently caused by the use of nitrofurantoin (Furadantin). Since then, no further reports of this untoward effect of the drug have appeared in the literature. Recently a case of acute pyelonephritis treated with Furadantin, observed in the Paediatric Department of the Poriah Government Hospital in Tiberias, developed s...

متن کامل

Haemolytic anaemia as first manifestation of Wilson's disease: a report of two cases.

Wilson's disease can have different manifestations like jaundice, cirrhosis of liver, extrapyramidal symptoms and dementia. Haemolytic anaemia may occur but it is commonly associated with florid manifestation of liver disease. Sometimes, liver cell necrosis can release huge free copper ions in blood, giving rise to oxidant damage to erythrocytes. Oxidative damage to cell membrane, haemoglobin a...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Archives of disease in childhood

دوره 46 245  شماره 

صفحات  -

تاریخ انتشار 1971