Mw. Sung et al., Sclerotherapy with picibanil (OK-432) for congenital lymphatic malformation in the head and neck, LARYNGOSCOP, 111(8), 2001, pp. 1430-1433
Hypothesis/Objectives: Congenital lymphatic malformations of the head and n
eck (LMHN) present special challenges to the otolaryngologist-head and neck
surgeon. Recently, a number of sclerotherapy trials have shown promising r
esults. In this study, we present our experiences with picibanil (OK-432) s
clerotherapy for this lesion. Study Design: Retrospectively review. Methods
: We retrospectively reviewed 21 patients who have undergone selerotherapy
with picibanil for LMHN. Results: Satisfactory response with complete or ne
arly complete shrinkage of the lesions was observed in 15 cases after repea
ted sclerotherapy (average, two times). We did not observe any significant
morbidity or complications in the patients treated with picibanil. Reductio
n in size of the mass was achieved in weeks to months. Some of the patients
who had not had any other previous treatment showed remarkable reductions
in size even after the first therapy. When we used picibanil sclerotherapy
as a primary treatment for the LMHN, most of our patients showed satisfacto
ry results regardless of the size or location of the lesions. Conclusion: G
iven with our experience and the reports that failure of picibanil scleroth
erapy does not hinder subsequent surgical salvage procedures, we recommend
trying picibanil sclerotherapy as a primary treatment for the LMHN and perf
orming surgical excision as a secondary modality if the response to the scl
erotherapy is not satisfactory.