Cryosurgery during topical imiquimod: a successful combination modality for lentigo maligna

Background  Either cryosurgery or topical imiquimod have been used to treat patients with lentigo maligna in cases where surgery is not feasible. Methods  We report a patient with lentigo maligna, who was treated with the combination of topical imiquimod and cryosurgery, and review the rationale, wh...

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Veröffentlicht in:International journal of dermatology 2008-05, Vol.47 (5), p.519-521
Hauptverfasser: Bassukas, I. D., Gamvroulia, C., Zioga, A., Nomikos, K., Fotika, C.
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Sprache:eng
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Zusammenfassung:Background  Either cryosurgery or topical imiquimod have been used to treat patients with lentigo maligna in cases where surgery is not feasible. Methods  We report a patient with lentigo maligna, who was treated with the combination of topical imiquimod and cryosurgery, and review the rationale, which led us to design the present combined cryo‐immunological treatment modality. Results  Sustained clearance of lentigo maligna to date (26 months after treatment). The successful treatment of this patient was based on the following rationale: A cryosurgery session during continuing imiquimod application may: (i) reinforce apoptosis of tumor cells; (ii) strengthen antiangiogenesis in the treated tumor; and (iii) build‐up a potent tumor‐destructive immune response by a cascade of events starting with imiquimod‐promoted attraction of immature dendritic antigen‐presenting cells (DCs) into the tumor. DCs further mature within the tumor‐antigen‐rich environment of subsequently cryo‐destructed tumor and upon imiquimod‐driven migration into the peripheral lymph nodes can stimulate a specific antineoplastic cell‐mediated immunity. Finally, continuing imiquimod application after cryosurgery may increase recruitment of activated effector cells into the tumor tissue leading to its destruction. Conclusion  Cryosurgery during continued topical imiquimod seems to be a promising treatment for lentigo maligna.
ISSN:0011-9059
1365-4632
DOI:10.1111/j.1365-4632.2008.03562.x