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DOI 10.1002/jbio.201800075

Медицинская библиотека · Journal of biophotonics · 2018

Argon plasma coagulation of actinic keratoses imaged by optical coherence tomography: An in vivo study indicating a possible lesion-directed treatment.

Schmitz Lutz, Hessam Schapoor, Scholl Lisa, Reitenbach Sarah, Segert Marc H, Gambichler Thilo, Stockfleth Eggert, Bechara Falk G

Клиническое исследованиеСтатьяПеревод пока не подготовлен

Аннотация

Actinic keratoses (AKs) can progress into invasive squamous cell carcinoma and thus may become a life threatening disease. Argon plasma coagulation (APC) might complement the therapeutic armamentarium in particular for AK lesions. However, there is no data on APC-induced micromorphological changes following the treatment of AKs. We aimed to determine in vivo APC-induced effects on the epidermis and dermoepidermal junction (DEJ) zone in AK lesions. We performed APC in 108 AKs using the spray mode with a power setting of 15 W and a flow rate of 2.0 L/min. Before and after the intervention, optical coherence tomography (OCT) was performed. After APC, 74.2% (46/62) lesions presented with clearly demarcated DEJ and without any epidermal tissue left, 25.8% (16/62) of treated lesions showed residual epidermal tissue left. In 19.4% (12/62), parts of the DEJ and in 6.5% (4/62), the entire DEJ could not be discriminated. The χ2 test showed a significant (P = 0.0025) association between the presence of hyperkeratosis prior to APC and intact DEJ after APC. In conclusion, APC as shown by OCT is a well controllable treatment modality for AKs causing only limited damage to dermal tissue. Further studies are needed to evaluate clinical outcome as well as recurrence rates.

Для цитирования: Schmitz Lutz, Hessam Schapoor, Scholl Lisa, Reitenbach Sarah, Segert Marc H, Gambichler Thilo, Stockfleth Eggert, Bechara Falk G. Argon plasma coagulation of actinic keratoses imaged by optical coherence tomography: An in vivo study indicating a possible lesion-directed treatment.. Journal of biophotonics. 2018. DOI: 10.1002/jbio.201800075.

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