original diagnosis of CLL.
autoimmune hemolytic anemia
original diagnosis of CLL.
autoimmune hemolytic anemia
evaluation
problem list: anemia/fatigue, hepatosplenomegaly, icterus, PMHx of URTI/CLL
acalabrutinib (a BTK inhibitor)
-brutinib is tyrosine kinase BTK inhibitor
extremities
subacute combined degeneration due to B12 deficiency. DCML, spinocerebellar, and lateral CST tract affected
factors in this patient's history
rough pregnancy, history of anemia, over 40 years old
bone marrow aspiration
estimate iron stores in bone marrow and hyperplasia of RBCs, megakaryocyte hyperplasia.
causes of iron deficiency in adults
poor diet, gastrectomy, peptic ulcer, colon polyps DJI iron fist bro (iron, folate, B12)
etiology of her anemia?
<3% is an underproduction issue, microcytic likely cause is blood loss from menorrhagia
probable uterine mass
leimyoma is common in women older than 40
treatment
prenatal vitamins, folate
microcytic anemia that you analyze and determine to be due to iron deficiency.
unexplained IDA is not a final diagnosis-> most concerning cause is bullemia
How did this problem come about?
diet, prenatal vitamins, etc
ferritin = 8
usually on wards anything <50 is abnormal
leading hypothesis
folate deficiency-> macrocytosis iron deficiency -> microcytosis normal MCV is due to some very large, some very small RBCs
MCV 81
normocytic anemia
differential: renal insufficiency, autoimmune disease, IDA, bowel absorption issue, folate deficiency, tapeworm, hemolytic anemia
Impression
too much lipid--> in liver disease and thalassemia, target cells can form
Another significant problem is of course her chest pain
acute chest syndrome explains murmur and chest pain
G6PD assay during the acute hemolytic reaction
FALSELY normal instead of LOW: G6PD-deficient red blood cells, specifically the older, more deficient ones, are destroyed during hemolysis, leaving behind younger, reticulocyte-rich cells with higher G6PD activity. A true G6PD deficiency is diagnosed using a genotyping test or retesting the patient after the hemolytic episode has resolved
G6PD deficiency
Heinz bodies
Make a list of drugs and/or chemicals which may lead to hemolytic anemia due to G6PD deficiency. What other conditions can "trigger" hemolysis
TMP-SMX, fava bean, dapsone, primaquine, moth balls
Why is the bilirubin elevated
heme is source of bilirubin, which is probably source of elevated unconjugated bilirubin.
high AST and normal ALT: RBCs have AST but not ALT inside them, so this represents more RBC breakdown as opposed to liver damage (both would be elevated).
Reticulocyte count
higher reticulocyte=hemolysis
need LDH, bilirubin, haptoglobin, blood smear, Coombs test (looking for antibodies stuck to RBC), DAT (direct= RBCs have antibiotics already attached), IAT (indirect=Ab in plasma)
imaging with ultrasound
look for stones or prostatic obstruction
benign enlargement
mechanical obstruction can lead to increased infection risk