Department of Dermatology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Photodermatol Photoimmunol Photomed. 2010 Dec;26(6):297-302. doi: 10.1111/j.1600-0781.2010.00546.x.
As different tissue types have distinct capabilities to accumulate protoporphyrin IX, fluorescence diagnosis with aminolevulinic acid-induced porphyrins (FDAP) could be used to discriminate between different types of tissue. Previous results demonstrated higher fluorescence ratios in squamous cell carcinoma (SCC) compared with actinic keratoses (AKs).
The lesional : non-lesional fluorescence ratio of AKs was compared with the ratio of SCC. Other factors influencing macroscopic fluorescence were also assessed, including stratum corneum thickness, which has been demonstrated to account for heterogeneous fluorescence in psoriasis and in AKs.
After 1 week of keratolytic pretreatment, FDAP was performed in 13 patients with 36 lesions suspected for AK or SCC. Biopsies were taken for histopathological diagnosis and measurement of stratum corneum thickness.
No significant differences were found in the fluorescence ratio (lesional : non-lesional skin) between AKs and SCCs, although macroscopic fluorescence was significantly higher in Bowen's disease and micro-invasive SCCs.
There could be a potential applicability of FDAP to differentiate premalignant lesions with a tendency to progress into SCC and squamous cutaneous lesions already progressing into early invasive cancer from other squamous cutaneous (pre)malignancies. The amount of hyperkeratosis, invasiveness and degree of differentiation seem to be responsible for variations in fluorescence intensity.
由于不同组织类型对原卟啉 IX 的积累能力不同,因此可以使用氨基酮戊酸诱导的卟啉(FDAP)荧光诊断来区分不同类型的组织。先前的结果表明,与光化性角化病(AK)相比,鳞状细胞癌(SCC)具有更高的荧光比值。
比较 AK 的病变与非病变荧光比值与 SCC 的比值。还评估了其他影响宏观荧光的因素,包括角质层厚度,已经证明其在银屑病和 AK 中存在异质性荧光。
在角质层松解预处理 1 周后,对 13 名疑似 AK 或 SCC 的 36 个病变患者进行 FDAP。对活检进行组织病理学诊断和角质层厚度测量。
AK 和 SCC 之间的荧光比值(病变:非病变皮肤)没有显著差异,尽管 Bowen 病和微浸润 SCC 的宏观荧光明显更高。
FDAP 可能适用于区分有进展为 SCC 倾向的癌前病变和已经进展为早期浸润性癌的鳞状皮肤病变,以及其他鳞状皮肤(前)恶性肿瘤。角化过度、侵袭性和分化程度似乎是荧光强度变化的原因。