Literature DB >> 24656411

An open-label study to evaluate sildenafil for the treatment of lymphatic malformations.

Christina Danial1, Andrea L Tichy1, Umar Tariq2, Glenda L Swetman1, Phuong Khuu1, Thomas H Leung1, Latanya Benjamin1, Joyce Teng1, Shreyas S Vasanawala2, Alfred T Lane3.   

Abstract

BACKGROUND: Lymphatic malformations can be challenging to treat. Mainstay interventions including surgery and sclerotherapy are invasive and can result in local recurrence and complications.
OBJECTIVE: We sought to assess the effect of 20 weeks of oral sildenafil on reducing lymphatic malformation volume and symptoms in children.
METHODS: Seven children (4 boys, 3 girls; ages 13-85 months) with lymphatic malformations were given oral sildenafil for 20 weeks in this open-label study. The volume of the lymphatic malformation was calculated blindly using magnetic resonance imaging performed before and after 20 weeks of sildenafil. Lymphatic malformations were assessed clinically on weeks 4, 12, 20, and 32. Both the physician and parents evaluated the lymphatic malformation in comparison with baseline.
RESULTS: Four subjects had a lymphatic malformation volume decrease (1.0%-31.7%). In 2 subjects, despite a lymphatic malformation volume increase (1.1%-3.7%), clinical improvement was noted while on sildenafil. One subject had a 29.6% increase in lymphatic malformation volume and no therapeutic response. Lymphatic malformations of all 6 subjects who experienced a therapeutic response on sildenafil softened and became easily compressible. Adverse events were minimal. LIMITATIONS: A randomized controlled trial will be necessary to verify the effects of sildenafil on lymphatic malformations.
CONCLUSIONS: Sildenafil can reduce lymphatic malformation volume and symptoms in some children.
Copyright © 2014 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.

Entities:  

Keywords:  congenital; lymphatic malformation; macrocystic; magnetic resonance imaging; microcystic; phosphodiesterase-5 inhibitors; sclerotherapy

Mesh:

Substances:

Year:  2014        PMID: 24656411      PMCID: PMC4024322          DOI: 10.1016/j.jaad.2014.02.005

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


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