F. Blei et al., THE RESPONSE OF PAROTID HEMANGIOMAS TO THE USE OF SYSTEMIC INTERFERONALFA-2A OR CORTICOSTEROIDS, Archives of otolaryngology, head & neck surgery, 123(8), 1997, pp. 841-844
Objective: To evaluate medical treatment for hemangiomas involving the
parotid area with or without other areas of involvement. Design: Retr
ospective analysis of pediatric patients treated medically for prolife
rative hemangiomas of the parotid region with or without hemangiomas i
n other regions. Indication for treatment included respiratory symptom
s relating to hemangiomas of the upper airway, difficulty feeding, rap
id rate of growth of the hemangioma, and deformity or obstruction of t
he ear canal. Setting: New York University Multidisciplinary Vascular
Anomaly Conference, New York, NY, and the Pediatric Oncology Departmen
t of Ospedale Pediatrico Bambino Gesu, Rome, Italy. Patients: Thirteen
patients with proliferative hemangiomas in the parotid area were trea
ted medically to inhibit growth and enhance involution of the hemangio
ma. Intervention: Six patients were treated with corticosteroids alone
(2-1 mg/kg daily). Two patients were treated with corticosteroids (2-
4 mg/kg daily) followed by interferon alfa-2a (3 million U/m(2) daily)
because of a failure to respond to corticosteroid therapy. One patien
t was treated with interferon alfa-2a alone (3 million U/m(2) daily).
Four patients were initially treated with interferon alfa-2a, then tre
ated with corticosteroids. One of these patients required intralesiona
l corticosteroid therapy for a massively enlarged lip and is therefore
included in this group. The other patient was given oral corticostero
ids for unknown reasons at another institution. In the remaining 2 pat
ients, there was no response to the use of interferon alfa-2a. Main Ou
tcome Measures: The size, bulk, and symptoms relating to the hemangiom
as of the patients were assessed. Results: None of the patients had a
significant improvement of the lesions of the parotid hemangiomas. In
contrast, for those patients with clinical symptoms due to hemangiomas
elsewhere or with cutaneous involvement typical of hemangiomas, the s
ymptoms improved with either of the above therapies, and the cutaneous
areas demonstrated signs of involution. Conclusions: The results in t
he 13 patients in this article demonstrate that hemangiomas in certain
anatomic sites, such as the parotid area, may be more resistant to th
erapy with corticosteroids or interferon alfa-2a. Differences in drug
metabolism, caliber of blood vessels, and/or blood flow in the parotid
gland may account for this observation.