Haemoglobin H disease (alpha-thalassemia): All in the family
The present case has been reported in The National Medical Journal of India.

An 18-year-old man had persistent anaemia not responding to iron and vitamin B12 supplements, and splenomegaly. Investigations showed a haemoglobin level of 6.7 g/dl, mean corpuscular volume (MCV) of 70.2 fL, mean corpuscular haemoglobin of 18.0 pg/dl, iron studies were normal and the lactate dehydrogenase level was 243 i.u./L. The peripheral smear revealed severe microcytic hypochromic anaemia with polychromasia.

The histogram of red blood cell (RBC) size showed a marked shift to the left and a high take-off from the Y-axis ([Figure 1]). We suspected thalassaemia or haemoglobinopathy. High-performance liquid chromatography (HPLC) done on Biorad D-10 revealed two fast peaks at <0.65 minute retention time, indicating haemoglobin H (HbH) disease. Methylene blue stained peripheral smear revealed a golf ball appearance of the erythrocytes with numerous HbH inclusions, indicative of HbH disease.

Screening of the family members was recommended.
The mother had RBC indices suggestive of a thalassaemia carrier, normal HPLC but occasional HbH inclusions. The father's values were normal. The brother's RBC histogram, HPLC and methylene blue-stained smear were similar to that of this patient.

Major takeaways:-
- Detection of alpha thalassaemia is important because it is common, but may remain silent or can manifest with haemolysis in HbH disease (alpha thalassaemia with three chain deletion), and have implications for genetic counselling.

- The RBC histogram is of crucial importance in diagnosis. Methylene blue stain may help in cases with low MCV, suggestive of thalassaemia silent carrier, if the haemoglobin A2 is normal or reduced, especially when patients cannot afford expensive confirmatory tests.

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Dr. S●●●●●●●●r P●●●●●a
Dr. S●●●●●●●●r P●●●●●a Pathology
Beautifully presented.... Informative. Thank you.
Dec 2, 2018Like1