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Murine Model of Leukemia Relapse to Induction Chemotherapy for Acute Lymphoblastic Leukemia
Published on: October 17, 2025
Extensive skeletal lesions in childhood acute lymphoblastic leukemia
1Department of Paediatrics, Bangabandhu Sheikh Mujib Medical University, Shahbag, Dhaka, Bangladesh.
Insights
This case highlights a child with unusual bone pain and swelling initially misdiagnosed as Langerhan
Area of Science:
- Pediatric Oncology
- Skeletal Radiology
- Hematology
Background:
- Childhood leukemia often presents with non-specific symptoms.
- Skeletal involvement in Acute Lymphoblastic Leukemia (ALL) can mimic other bone diseases.
- Early and accurate diagnosis is crucial for effective treatment and improved outcomes.
Observation:
- A 2-year-old boy presented with fever, joint pain, and swelling, initially suspected to be Langerhan's cell histiocytosis.
- Radiological findings revealed destructive bone lesions, osteolytic lesions, and periosteal reactions.
- Hematological tests indicated high WBC, low platelets, lymphoblasts, elevated LDH, and uric acid.
Findings:
- Bone marrow aspiration and immunophenotyping confirmed pre-B Acute Lymphoblastic Leukemia (ALL).
- Extensive skeletal involvement was evident, including leukemic lines and subperiosteal new bone formation.
- The patient showed significant improvement with protocol-based chemotherapy.
Implications:
- Increased awareness of diverse skeletal manifestations in childhood ALL is essential for accurate diagnosis.
- Skeletal symptoms like limb pain and swelling in children warrant thorough investigation for underlying leukemia.
- Timely diagnosis of ALL is critical due to its curability compared to metastatic cancers.
Abstract:
A 2 years old male child was admitted in Dhaka Shishu Hospital with one month history of fever, swelling and pain in joints of right leg. Hematological and microbiological investigation revealed normal except radiological findings when there were destructive lesions of affected bones and thought to be Langerhan's cell histiocytosis but did not respond to treatment. Subsequently, he was transfer to Pediatric Hematology and Oncology, Bangabandhu Sheikh Mujib Medical University (BSMMU) for proper management. On examination, the boy was mildly pale, severe bone pain, no organomegaly but few occipital group of lymphnode were palpable. He had extensive red tender swelling over the hands and legs. Hematological values showed high WBC, low platelet count and lymphoblasts. Biochemical values were high serum LDH and serum uric acid. Skeletal survey showed diffuse osteolytic lesion and osteoporosis with evidence of transverse metaphyseal radiolucent bands (leukemic line), lamellar periosteal reactions and cortical erosions widespread throughout the skeleton with subperiosteal new bone formation. Radioisotop of skeleton showed increase uptake at the site of lesions. Bone marrow aspiration findings were suggestive of ALL-L1 and cytochemistry of aspirate showed PAS positive and Sudan black negative. Immunophenotype confirmed as pre-B ALL, Then, protocol based induction had given for 4 weeks. Thereafter, a short course of intensification followed by maintenance therapy had started with significant improvement of physical, hematological and radiological findings. So, an awareness of varied clinical and radiological manifestations of childhood ALL in bone marrow and skeletal system are needed in order to establish a correct diagnosis when the presenting signs and symptoms are enigmatic. It is also important to keep in mind the possibility of extensive skeletal involvement in ALL, especially when a child present with pain, swelling of limb with walking difficulties. The curability of ALL in contrast to metastatic malignancies makes accurate diagnosis of paramount importance.
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