Pathology EMQ
Name:
Candidate number:
Theme: Paediatric Haematology
OPTION LIST
|
A |
Alloimmune thrombocytopenic purpura |
I |
Haemophilia B |
|
B |
Alpha thalassaemia |
J |
Henoch-Schönlein Purpura |
|
C |
Autoimmune thrombocytopenic purpura |
K |
Hereditary spherocytosis |
|
D |
Beta thalassaemia major |
L |
Non-hereditary spherocytosis |
|
E |
Diamond-Blackfan anaemia |
M |
Sickle cell disease |
|
F |
Fanconi’s anaemia |
N |
Sickle cell HbD disease |
|
G |
G6PD deficiency |
O |
Sickle cell trait |
|
H |
Haemophilia A |
P |
TAR syndrome |
For each scenario below, choose the most appropriate answer from the list above. Each option may be used once, more than once or not at all.
1. A neonate is born clinically jaundiced. Red blood cells are osmotically fragile and a peripheral blood film shows that they are markedly small, without a central zone of pallor.
2. A neonate is born with widespread petechiae and purpurae, but is otherwise well. The WCC and Hb are normal, and the peripheral blood film does not show blast cells.
3. A routine heel prick test on a neonate born in Chandigarh identifies Hb S and another variant Hb.
4. A neonate is born in Bangkok Hospital at 28 weeks severely oedematous and pale, with a massive placenta, and dies within an hour of birth.
5. A neonate is born with shortened arms; thumbs and digits are present. Blood tests reveal a thrombocytopenia.
ANSWERS
|
1. K |
2. A |
3. N |
4. B |
5. P |