An 18-month-old boy with intermittent fever, weakness, some vomiting, and facial puffiness. There was no history of jaundice, bleeding, or transfusions.
Initial labs showed:
On the peripheral smear, we saw occasional blast cells, immature cells that can point to a blood cancer. That raised a careful question: Could this be leukaemia?
We performed a bone marrow aspiration and biopsy with a full leukaemia work-up. The marrow showed sheets of uniform blasts—cells with scant bluish cytoplasm, fine “open” chromatin, and typically 0–1 tiny nucleolus; a few showed nuclear grooves. Taken together, these features indicated B-cell Acute Lymphoblastic Leukaemia (B-ALL).
Plain English: the marrow was crowded with baby-like blood cells that hadn’t matured, classic for childhood B-ALL.
Flow cytometry (a detailed cell “fingerprint”) showed ~85.7% blasts with CD45 dim expression. The blasts were positive for CD10, CD19, HLA-DR, CD38, sCD22 and negative for CD20—a pattern that confirms B-ALL.
Plain English: the cancer cells wore the badge set typical of B-cell origin.
We started a standard BFM-2002–based chemotherapy regimen using Vincristine, Doxorubicin, Daunorubicin, L-asparaginase (Leunase), Methotrexate, 6-mercaptopurine, and Cytarabine.
After 1 month (end of induction):
The highly sensitive MRD test was negative—meaning remission. We proceeded to consolidation chemotherapy per NCCN guidance, and the child is now on oral maintenance.
Plain English: the first month hit the disease hard; the “deep-clean” test saw no detectable leukaemia cells, so we moved into phases designed to lock in the win and prevent a comeback.
Plain English: most children do very well with today’s treatments—and our patient’s path is very encouraging.
A toddler arrived tired and unwell; careful testing named the problem, modern chemo hit it hard, and one month later the deepest tests showed no trace, a small fighter firmly on the road to recovery.