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EMQs in Clinical Medicine.pdf - Peshawar Medical College

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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.

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