EMQs in Clinical Medicine.pdf - Peshawar Medical College
EMQs in Clinical Medicine.pdf - Peshawar Medical College
EMQs in Clinical Medicine.pdf - Peshawar Medical College
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
The peripheral blood film – answers 63<br />
22 The peripheral blood film<br />
Answers: E G A J B<br />
E<br />
G<br />
A<br />
J<br />
B<br />
Presence of Burr cells <strong>in</strong> a patient be<strong>in</strong>g treated <strong>in</strong> the ICU with<br />
multiple organ failure.<br />
Burr cells <strong>in</strong>dicate uraemia.<br />
Howell–Jolly bodies <strong>in</strong> a patient with coeliac disease.<br />
Howell–Jolly bodies are found <strong>in</strong> hyposplenism.<br />
Neutrophil hypersegmentation <strong>in</strong> a patient with paraesthesia <strong>in</strong> the<br />
f<strong>in</strong>gers and toes.<br />
Vitam<strong>in</strong> B 12 deficiency is a recognized cause of megaloblastic anaemia<br />
and, if left untreated, can lead to a polyneuropathy affect<strong>in</strong>g the peripheral<br />
nerves. There is early loss of vibration sense and proprioception<br />
because the posterior columns are affected first.<br />
Other changes <strong>in</strong> megaloblastic anaemia <strong>in</strong>clude chromat<strong>in</strong> deficiency,<br />
premature haemoglob<strong>in</strong>ization and the presence of giant metamyelocytes.<br />
Microcytic hypochromic film <strong>in</strong> a 24-year-old woman present<strong>in</strong>g with<br />
lethargy.<br />
Target cells are a feature of iron deficiency anaemia. Koilonychia (brittle<br />
spoon-shaped nails) are found <strong>in</strong> severe disease. Other rare signs <strong>in</strong>clude<br />
angular cheilosis and oesophageal web. The presence of an iron deficiency<br />
anaemia plus oesophageal web is known as the<br />
Plummer–V<strong>in</strong>son/Paterson–Brown–Kelly syndrome.<br />
Film of a 3-month-old baby boy shows a hypochromic microcytic<br />
anaemia with target cells and nucleated red blood cells. There are<br />
markedly high HbF levels.<br />
In -thalassaemia there is defective synthesis of cha<strong>in</strong>s with a severity<br />
that depends on the <strong>in</strong>heritance of the defect. A patient with thalassaemia<br />
m<strong>in</strong>or is an asymptomatic heterozygous carrier. The thalassaemia<br />
major patient is homozygous and usually presents <strong>in</strong> the first year of life<br />
with a severe anaemia and failure to thrive. The symptoms of anaemia<br />
start at this po<strong>in</strong>t because this is the period when cha<strong>in</strong> production is<br />
switched off and cha<strong>in</strong>s fail to form <strong>in</strong> adequate numbers.<br />
Blood transfusions are required to keep the Hb 9–10 g/dl. Iron<br />
chelators are required to protect the major organs from transfusionmediated<br />
iron overload. Ascorbic acid (vitam<strong>in</strong> C) can also be used to<br />
<strong>in</strong>crease ur<strong>in</strong>ary excretion of iron. The patient requires long-term folic<br />
acid supplements caused by the extreme demand associated with bone<br />
marrow hyperplasia.