scholarly journals Acute Pancreatitis as a Complication of Sickle Cell Anaemia

Reports ◽  
2018 ◽  
Vol 1 (3) ◽  
pp. 19
Author(s):  
Parisa Moori ◽  
Alexios Dosis ◽  
Zoheb Ahmad ◽  
Ambareen Kausar ◽  
Diana Triantafyllopoulou

A common cause of abdominal pain is acute pancreatitis, with the majority of cases being attributed to gallstones and excess alcohol. Sickle cell anaemia (SCA) is an autosomal recessive disease causing the production of abnormal haemoglobin. Physiological changes can lead to vaso-occlusion in sickle cell anaemia. Cholelithiasis is frequently seen in patients with SCA and complications from this can increase patient morbidity. We present a rare case of acute pancreatitis inducing a vaso-occlusive crisis.

Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 3802-3802 ◽  
Author(s):  
Julie Makani ◽  
Elineema Meda ◽  
Stella Rwezaula ◽  
Khadija Mwamtemi ◽  
Swee Lay Thein ◽  
...  

Abstract Background: The recognition of Sickle cell anaemia (SCA) as a problem of public health significance by the world health organisation in May 2006 has major implications in Africa where an estimated 300,000 children are born every year. In Tanzania, 20% of the population are heterozygous for the S Gene; up to 10,000 children are born every year with SCA. In order to target limited resources, research and interventional programmes require the identification of problem areas that will need to have maximum impact. Despite the protection against malaria in heterozygous individuals, paradoxically malaria is thought to be a common cause of morbidity and mortality in SCA. Bacterial infections have been implicated as a common cause of mortality and Transcranial Doppler ultrasonography (TCD) has been used to identify patients at increased risk of stroke, a recognised cause of morbidity. Aims: The study attempts to define causes of morbidity and mortality in SCA in Tanzania focusing on three major areas where it is important to establish clear answers. The aims of the study are to determine the role of malaria infection in SCA patients, to describe the major bacterial pathogens associated with admission in SCA patients and to describe the spectrum of cerebral blood flow velocities (CBFv) using TCD in SCA patients in East Africa. Study design: This is a prospective, descriptive cohort study in Muhimbili national hospital, Dar-es-salaam, Tanzania with clinical surveillance of patients in outpatient clinic every three months and during admission to hospital for any acute clinical event. Results: From March 2004 to June 2006, there have been 5,601 visits during which clinical and laboratory data has been collected on 1,000 (male 51.4%) SCA patients. The mean age of the patients is 10 7.4 years, (range 7 months54 yrs), with 91.7% below 20 years of age; 8.28% under the age of 5 years. The frequency of major clinical events, including fits (5.2%), stroke (1.9%) is reported. The prevalence of malaria parasitaemia in outpatients and during admission was 2.9% and 7.7% respectively which was lower than in the non-sickle population. There have been 516 admissions during this period, presenting with pain (44%), anaemia (17%) and fever (15%). Salmonella species (Non typhoid salmonella) was the commonest bacterial pathogens isolated. TCD was done in 400 patients (age 2 – 16 years); with 25% having a time averaged maximal mean velocity of 150 cms/second or more, suggesting stenosis. Conclusion: Preliminary analysis suggest over 90% of the SCA population are under 20 years of age, with a deficit in the under 5 year age group. There is reduced malaria infection, suggesting resistance to malaria and not susceptibility as previously reported. Painful crises were the commonest cause of admission with salmonella the most frequent pathogen isolated. TCD identified at least 25% of patients with CBFv suggestive of stenosis. This study is the initial step in describing the causes of morbidity in patients with SCD disease in Tanzania and will form the basis of longitudinal studies that will attempt to guide interventional strategies, target research and provide insight into natural history of SCD in East Africa.


2019 ◽  
Vol 38 (2) ◽  
pp. 128-131
Author(s):  
Nanda Kishwor Chaudhary ◽  
Ram Hari Chapagain ◽  
Sani Sipai ◽  
Suryakant Chaudhary ◽  
Krishan Prasad Paudel

Familial Chylomicronaemia is a rare autosomal recessive disease of lipoprotein metabolism characterized by deficiency or absence of lipoprotein lipase (LPL) or its co-factor apoC-II which causes severe elevation of triglyceride and chylomicron resulting in lipaemic plasma, recurrent attacks of acute pancreatitis, eruptive xanthomas, hepato-splenomegaly and lipaemiaretinalis. We report a case of term female neonate with lipaemic plasma, lipemia retinalis, markedly elevated triglyceride level which is consistent with diagnosis of Familial Chylomicronaemia. Keywords: Familial Chylomicronemia, lipemic plasma, triglyceride level, Lipemia retinalis


2016 ◽  
Vol 10 (2) ◽  
pp. 73-81 ◽  
Author(s):  
Anietie Ekong

The haemoglobinopathies are the most common monogenetic diseases in the world. They include the thalassaemias and sickle cell syndromes. The sickle cell syndromes encompass several abnormal haemoglobin variants, of which homozygosity for the sickle cell gene – that is, sickle cell anaemia is the most common and most severe. Originally characteristic of the tropics and subtropics, recent mobility and migratory trends have meant that the prevalence of sickle cell disease (SCD) has significantly increased in the UK. It is important that GPs have an understanding of this disease, in order to help their patients deal with complications of every-day life. This article will address three main aspects of SCD: diagnosis, health maintenance, and some acute and chronic complications of SCD.


Anemia ◽  
2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
A. Ganguly ◽  
W. Boswell ◽  
H. Aniq

Sickle cell anaemia is an autosomal recessive genetic condition producing abnormal haemoglobin HbS molecules that result in stiff and sticky red blood cells leading to unpredictable episodes of microvascular occlusions. The clinical and radiological manifestations of sickle cell anaemia result from small vessel occlusion, leading to tissue ischemia/infarction and progressive end-organ damage. In this paper we discuss and illustrate the various musculoskeletal manifestations of sickle cell disease focusing primarily on marrow hyperplasia, osteomyelitis and septic arthritis, medullary and epiphyseal bone infarcts, growth defects, and soft tissue changes.


2021 ◽  
Vol 7 (3) ◽  
pp. 1-3
Author(s):  
Benoy Varghese ◽  

Cystinosis is a rare autosomal recessive disease characterized by cystine accumulation in the lysosome leading to various organdysfunction. Kidneys are severely affected, of which nephropathic infantile form is the most common.


2021 ◽  
Vol 12 ◽  
Author(s):  
David C.-Y. Lu ◽  
Rasiqh Wadud ◽  
Anke Hannemann ◽  
David C. Rees ◽  
John N. Brewin ◽  
...  

Red cells from patients with sickle cell anaemia (SCA) contain the abnormal haemoglobin HbS. Under hypoxic conditions, HbS polymerises and causes red cell sickling, a rise in intracellular Ca2+ and exposure of phosphatidylserine (PS). These changes make sickle cells sticky and liable to lodge in the microvasculature, and so reduce their lifespan. The aim of the present work was to investigate how the peculiar conditions found in the renal medulla – hypoxia, acidosis, lactate, hypertonicity and high levels of urea – affect red cell behaviour. Results show that the first four conditions all increased sickling and PS exposure. The presence of urea at levels found in a healthy medulla during antidiuresis, however, markedly reduced sickling and PS exposure and would therefore protect against red cell adherence. Loss of the ability to concentrate urine, which occurs in sickle cell nephropathy would obviate this protective effect and may therefore contribute to pathogenesis.


2000 ◽  
Vol 111 (4) ◽  
pp. 1194-1197 ◽  
Author(s):  
A. O. Emeribe ◽  
A. E. Udoh ◽  
M. H. Etukudoh ◽  
C. C. Okany ◽  
M. Kehinde ◽  
...  

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