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Correspondence and communication| Volume 65, ISSUE 8, P1124-1126, August 2012

Reply to the letter to the Editor on “Low-dose propranolol for infantile haemangioma”

Published:January 24, 2012DOI:https://doi.org/10.1016/j.bjps.2012.01.001
      We thank you for the opportunity to respond to Dr Zheng’s letter regarding our article, Low-Dose Propranolol for Infantile Haemangioma.
      • Tan S.T.
      • Itinteang T.
      • Leadbitter P.
      Low-dose propranolol for infantile haemangioma.
      The serendipitous discovery of accelerated involution of infantile haemangioma induced by propranolol
      • Leaute-Labreze C.
      • Dumasde la Roque E.
      • Hubiche T.
      • Boralevi F.
      • Thambo J.B.
      • Taieb A.
      Propranolol for severe hemangiomas of infancy.
      and acebutalol
      • Bigorre M.
      • Van Kien A.K.
      • Huguette V.
      Beta-blocking agent for the treatment of infantile hemangioma.
      has resulted in a paradigm shift in the management for this condition. This mirrors the previous serendipitous observation of the effect of high dose steroids on infantile haemangioma
      • Zarem H.A.
      • Edgerton M.T.
      Induced resolution of cavernous hemangiomas following prednisolone therapy.
      which naturally invited logical questions on the (1) mechanism of action; (2) the optimal dose regimen and duration of treatment; and (3) the side effects of treatment in infants and young children with problematic infantile haemangioma. Over the last 40 years, some of these questions have been answered and the dose regimen settled on 2–3 mg/kg/day
      • Boon L.M.
      • MacDonald D.M.
      • Mulliken J.B.
      Complications of systemic corticosteroid therapy for problematic hemangioma.
      but the mechanism of action of steroid therapy remains incompletely elucidated with induced apoptosis through the up-regulation of mitochondrial cytochrome b gene being proposed.
      • Hasan Q.
      • Tan S.T.
      • Gush J.
      • Peters S.
      • Davis P.F.
      Steroid therapy of a hemangioma: histochemical and molecular changes.
      • Hasan Q.
      • Tan S.T.
      • Gush J.
      • Davis P.F.
      Altered mitochondrial cytochrome b gene expression during the regression of hemangioma.
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      References

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          We present a 55 year old female, with gradual painless thickening of her eyelids and nose over several months, who requested aesthetic surgery to correct these changes. One-year prior to this she had undergone a craniotomy and debulking of an olfactory groove meningioma and commenced on prophylactic phenytoin therapy. On examination she was found to have a widened nasal bridge and soft-tissue thickening of the glabellar region and medial canthi. (Figure 1a). Her paranasal and eyelid thickening was presumed to be phenytoin-related and under the supervision of her neurologist this was tailed off.
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