UOC Dermatologia, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti, Università degli Studi di Milano, Milan, Italy.
Dermatol Ther. 2021 Jan;34(1):e14706. doi: 10.1111/dth.14706. Epub 2021 Jan 3.
Hidradenitis suppurativa (HS) is a debilitating skin disease presenting with nodules, abscesses, and fistulae preferentially in the main folds. Adalimumab is the only licensed biologic for moderate-to-severe HS. Ultrasound demonstrated good sensitivity to provide anatomic and functional information in HS; in particular assessing vascularization, related to inflammation, and fibrosis in HS lesions before and after adalimumab treatment with ultrasound and Color Doppler may integrate clinical evaluation with imaging. Patients with moderate-to-severe HS were enrolled in this observational prospective study. Clinical evaluation (according to Hurley classification and International Hidradenitis Suppurativa Severity Score System score) and ultrasound (according to US HS-PGA)/Color Doppler were performed at baseline and after 12 weeks of adalimumab. Ultrasound was used for assessing fibrosis and Color Doppler for vascularization. For each patient, the three most severe lesions among abscesses and fistulae were chosen for total 96 lesions. Thirty-two patients were included, 18 men (56%) and 14 women (44%) with mean age 41.2. Mean IHS4 was 22.4 at baseline and dropped to 14.7 at week 12. Based on US HS-PGA, 14 out of 32 patients fell down by one or more classes of severity. Interestingly, adalimumab led to overall decrease in vascularization, particularly in lesions with intense vascular flow, which were 78 (81.3%) at baseline and became only 25 (26.04%). Finally, marked increase in fibrosis was seen after adalimumab, notably in lesions without fibrosis, which were 81 (84.4%) at baseline and became 15 (15.6%). This study confirms the efficacy of adalimumab in HS and provides value for vascularization and fibrosis as important ultrasonographic tools integrating clinical scores.
化脓性汗腺炎(HS)是一种使人衰弱的皮肤病,主要表现为结节、脓肿和瘘管,优先发生在主要褶皱处。阿达木单抗是唯一批准用于中重度 HS 的生物制剂。超声对提供 HS 的解剖和功能信息具有很好的敏感性;特别是在阿达木单抗治疗前后,通过超声和彩色多普勒评估 HS 病变的血管化情况,与炎症和纤维化相关,可能将临床评估与影像学相结合。本研究纳入了中重度 HS 患者。在基线时和阿达木单抗治疗 12 周后进行临床评估(根据 Hurley 分类和国际化脓性汗腺炎严重程度评分系统评分)和超声(根据 US HS-PGA)/彩色多普勒。超声用于评估纤维化,彩色多普勒用于评估血管化。每位患者从脓肿和瘘管中选择三个最严重的病变,共 96 个病变。共纳入 32 例患者,其中男性 18 例(56%),女性 14 例(44%),平均年龄为 41.2 岁。基线时 IHS4 平均为 22.4,治疗 12 周后降至 14.7。根据 US HS-PGA,32 例患者中有 14 例下降了一个或多个严重程度级别。有趣的是,阿达木单抗导致血管化总体减少,特别是在血管血流强烈的病变中,基线时为 78 例(81.3%),治疗 12 周后仅为 25 例(26.04%)。最后,阿达木单抗治疗后纤维化明显增加,特别是在无纤维化的病变中,基线时为 81 例(84.4%),治疗 12 周后为 15 例(15.6%)。本研究证实了阿达木单抗在 HS 中的疗效,并提供了血管化和纤维化作为重要的超声工具的价值,将临床评分与影像学相结合。