Severe Tacrolimus-Induced Granulomatous Rosacea Recalcitrant to Oral Tetracyclines

June 2015 | Volume 14 | Issue 6 | Case Reports | 628 | Copyright © June 2015


Lissy Hu BA,a Christina Alexander BA,b Nicole F. Velez MD,c F. Clarissa Yang MD,c
Alvaro Laga Canales MD MMSc,c,d Stephanie Liu MD,c and Ruth Ann Vleugels MD MPHc,

aHarvard Medical School, Boston, MA
bDivision of Dermatology, University of Arizona, Tucson, AZ
cDepartment of Dermatology, Brigham and Women’s Hospital, Boston, MA
dDepartment of Pathology, Brigham and Women’s Hospital, Boston, MA

D. folliculorum is one precipitant) plays a central role in the pathogenesis.10 Pimecrolimus cream, another topical calcineurin inhibitor, has also been reported to induce rosaceiform eruptions.11-14 However the eruptions associated with pimecrolimus cream, which is mostly water-based, are less severe than those reported with tacrolimus ointment due to the occlusive properties of the latter.11
To the best of our knowledge, severe GR induced by tacrolimus and recalcitrant to tetracyclines has not previously been reported. In prior case reports, patients improved within a few months after topical tacrolimus was withdrawn and oral doxycycline or minocycline was initiated. The severity of this patient’s eruption may correspond to the duration of tacrolimus use, which spanned multiple years, given that topical tacrolimus can disrupt epidermal permeability and antimicrobial function by impairing skin-barrier recovery, as shown in recent studies.15 These barrier-recovery deficiencies, acquired over long-term use of tacrolimus, may have predisposed our patient to a more severe eruption and protracted recovery. Accordingly, our patient required aggressive treatment with multiple topical therapies in conjunction to oral tetracyclines.
Topical tacrolimus is generally a well-tolerated medication that is used successfully for a variety of conditions. Although tacrolimus-induced granulomatous rosacea is rarely reported, recognition of the entity is important, and successful treatments strategies may include combining systemic and topical therapies with chemical peels.

DISCLOSURES

The authors have no conflicts of interest to declare.

REFERENCES

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AUTHOR CORRESPONDENCE

Previous presentations of this manuscript: Presented in poster form at the International Investigative Dermatology meeting 2013