a 19 year girl was admitted in fmw with complains of fever with chills and rigor abdominal pain loose motion on examination pallor hepatosplenomegaly was present past history of same complains was present three to four times with in 6 month past history of pcod. severe hypomenorrhoea and 2 BT WAS DONE. I POSTED present cbc findings ps blood image and sickling test images......may be useful and rare to find intresting case.....give ur expert opinion thanks



Sickle cell anemia

Sickle cell disease.

Sickle cells seen

Sickle cell disease

?Sickle cell disease Adv- Hb typing

Nice Sickle cell disease

Moderate aniso poikilocytosis hypochromia Fair number of microcytes.targets.schistocytes Dacryocytes.leptocytes.irregularly contracted cells and many sickle cells. Many polychromatic cells noted. SICKLE CELL DISEASE. As hepatosplenomegaly is present..a sickle beta thalassemia or compound hemoglobinopathy is likely. Sug.clinical correlation HPLC.Hb electrophoresis Cbc

Sickle cell disease with possible iron deficiency anemia

Sickle cell anemia

Sickel cell Anemia

Sickle cell crisis
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