2009
DOI: 10.1002/ppul.21139
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Acute pulmonary toxicity following intralesional administration of bleomycin for a lymphovenous malformation

Abstract: This case illustrates the importance of early recognition and aggressive treatment of acute bleomycin toxicity resulting from intralesional administration of this medication for lymphovenous malformations.

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Cited by 37 publications
(22 citation statements)
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“…There has been one reported case of pulmonary toxicity following IBI in a lymphatic malformation in over 2600 patients in the literature [24]. This unit treats most patients with a dose of 0.5 mg/kg, which is in keeping with the published studies.…”
Section: Discussionsupporting
confidence: 56%
“…There has been one reported case of pulmonary toxicity following IBI in a lymphatic malformation in over 2600 patients in the literature [24]. This unit treats most patients with a dose of 0.5 mg/kg, which is in keeping with the published studies.…”
Section: Discussionsupporting
confidence: 56%
“…However, pulmonary pneumonitis and fibrosis are very rarely listed in the literature as complications of percutaneous bleomycin sclerotherapy. We are aware of two such reports . Both of these involved young children with small body surface area, which may indicate the need for a greater margin of safety in smaller people.…”
Section: Discussionmentioning
confidence: 99%
“…We are aware of two such reports. 52,53 Both of these involved young children with small body surface area, which may indicate the need for a greater margin of safety in smaller people.…”
Section: Bleomycin As a Sclerosant For The Treatment Of Symptomatic Vmsmentioning
confidence: 99%
“…39,49 A common institutional dose policy is 0.5 to 1 mg/kg with a single-session maximum dose of 15 mg. To date, no percutaneous sclerotherapy-associated cases of pulmonary fibrosis have been reported, although a single case of acute lung toxicity from bleomycin treatment of a vascular malformation has been reported. [50][51][52] A small prospective study of pediatric patients with microcystic LMs undergoing percutaneous bleomycin sclerotherapy showed no significant changes in chest radiography and pulmonary function tests 6 and 12 months following treatment, and abnormalities in diffusing capacity of the lungs for carbon monoxide and vital capacity have been described as most sensitive and specific for bleomycin-induced damage, respectively. 39 Importantly, because of the rarity of pulmonary complications associated with bleomycin sclerotherapy (with adherence to dose limits), it is not common practice to obtain preprocedure chest X-rays or pulmonary function tests.…”
Section: Bleomycinmentioning
confidence: 99%