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Updated: Jul 22, 2025

Chemotherapy-induced Vascular Toxicity - Real-time In vivo Imaging of Vessel Impairment
Published on: January 7, 2015
Delayed presentation of vincristine extravasation.
Saba Ghaffary1, Nasrin Gholami1, Sama Samankan2
1Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Vincristine extravasation, a severe chemotherapy complication, can cause tissue necrosis. A case study shows a successful treatment approach using betamethasone cream, DMSO, and levofloxacin for delayed vincristine extravasation.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Vincristine is a vesicant chemotherapy agent that can cause extravasation, leading to tissue necrosis and oncological emergencies.
- Extravasation occurs when chemotherapy leaks from the intended vessel into surrounding perivascular tissue.
Observation:
- A 29-year-old woman with B-cell acute lymphoblastic leukemia (ALL) on maintenance chemotherapy (POMP regimen) developed symptoms 48 hours after intravenous vincristine administration.
- Symptoms included burning, pain, and tenderness at the injection site, progressing to a large brown lesion within 7 days.
Findings:
- The patient was treated with betamethasone cream, dimethyl sulfoxide (DMSO) solution, and oral levofloxacin.
- Complete lesion improvement was observed within 10 days of initiating this therapy, with no significant adverse events.
Implications:
- This clinical approach demonstrated a beneficial effect in managing delayed vincristine extravasation.
- The findings suggest this treatment strategy could be considered for similar cases, especially when standard antidote therapies are ineffective.
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