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December 1987

Panniculitis Associated With Severe a1-Antitrypsin Deficiency: Treatment and Review of the Literature

Author Affiliations

From the Department of Dermatology, Mayo Clinic and Mayo Foundation, Rochester, Minn.

Arch Dermatol. 1987;123(12):1655-1661. doi:10.1001/archderm.1987.01660360083017

• Panniculitis associated with homozygous severe α1-antitrypsin deficiency was documented in three women hospitalized for painful cutaneous and subcutaneous ulcerations (severe panniculitis with spontaneous ulceration and drainage of clear or serosanguineous fluid). None had a history of trauma or infection. One patient responded rapidly and completely to treatment with dapsone. One patient, who had more extensive disease, failed to respond to prednisone plus dapsone; infusions of α1-proteinase inhibitor concentrate led to resolution of her panniculitis. One patient who had severe and extensive panniculitis and pleural effusions failed to respond to corticosteroids but did well when both dapsone and infusions of α1-proteinase inhibitor concentrate were added to her treatment program.

(Arch Dermatol 1987;123:1655-1661)

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