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



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

Siclkle cell disease. Degree of splenomegaly is not mentioned. if moderate to severe Adv Hemoglobin electrophoresis to exclude presence of Thallassemia minor.

Sickel cell Anemia

Sickle cell crisis

Sickle cell anaemia.

Sickle cell disease.

sickle cell anemia

?Sickle cell disease Adv- Hb typing

Nice Sickle cell disease

Sickle cell anaemia

Sickle cell disease

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