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Pure Red Cell Aplasia (PRCA) is
a rare blood disorder in which the bone marrow produces very few or no red
blood cell precursors. Unlike many other blood disorders, white blood cells
and platelets are usually produced normally. The resulting shortage of red
blood cells can cause severe anaemia and reduced oxygen delivery
throughout the body.
Possible triggers include autoimmune
disorders, certain viral infections, thymoma, medications, and other
underlying diseases. In some cases, it may be associated with inherited genetic
abnormalities.
Common symptoms are related
to anaemia and may include persistent tiredness, weakness, pale skin,
shortness of breath, dizziness, headaches, and reduced exercise tolerance.
Diagnosis generally involves a complete blood count, reticulocyte count, and bone marrow examination. The marrow typically shows a marked reduction or
absence of erythroid precursors while other cell lines remain relatively
preserved.
Treatment depends on the
underlying cause and severity. Options may include stopping a causative
medicine, treating an associated disorder, blood transfusions,
immunosuppressive therapy, or other specialist-directed treatments. Patients
with persistent PRCA require careful monitoring because prolonged
anaemia can significantly affect quality of life. Early diagnosis and
appropriate management can help restore red blood cell production and
prevent complications.