2020
DOI: 10.1007/s00270-020-02420-w
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Fatal Lung Toxicity After Intralesional Bleomycin Sclerotherapy of a Vascular Malformation

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Cited by 23 publications
(7 citation statements)
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“…[21][22][23] There has been a single report on fatal lung toxicity in a 15-month-old girl 1 week after injection of 7 units of bleomycin into a cheek macrocystic LM. 24 In the present study, adverse reactions noted were inflammation in 7 (29%) and transient hyperpigmentation in 12 (50%) of the patients. No long-term side effects occurred in any of the patients.…”
Section: Discussionsupporting
confidence: 48%
“…[21][22][23] There has been a single report on fatal lung toxicity in a 15-month-old girl 1 week after injection of 7 units of bleomycin into a cheek macrocystic LM. 24 In the present study, adverse reactions noted were inflammation in 7 (29%) and transient hyperpigmentation in 12 (50%) of the patients. No long-term side effects occurred in any of the patients.…”
Section: Discussionsupporting
confidence: 48%
“…By binding to the DNA of lymphatic endothelial cells (LECs), bleomycin inhibited DNA synthesis, cut DNA strands, damaged endothelial cells, thickened walls, narrowed the lumen, and eventually caused focal atrophy. However, bleomycin has dose-dependent pulmonary toxicity, and there is a risk of pulmonary fibrosis when the cumulative dose exceeds 160 mg. 24 Therefore, in this study, the cumulative dose of bleomycin did not exceed 15 mg. As a result, there was no pulmonary toxicity-related side effects. Simultaneously, lauromacrogol, a secondary sclerosing agent, was combined with bleomycin to destroy the cell membrane of LECs, cause organ fibrosis, prolong the action time of bleomycin in the lesion, reduce the amount of bleomycin, and accelerate luminal occlusion and lesion atrophy.…”
Section: Discussionmentioning
confidence: 90%
“…The most worrisome side-effect is pulmonary toxicity, which is less likely to occur in the doses used for sclerotherapy, occurring most commonly during its use in oncologic practice. However, anecdotal reports have noted this rare, non-immunologically mediated adverse effect after its use for sclerotherapy [12,13]. There have also been anecdotal reports of acute adverse effects including hyperpyrexia, hypotension, altered mental status, and respiratory distress during the administration of bleomycin for chemotherapy in oncology patients [11,14].…”
Section: Discussionmentioning
confidence: 99%