From the Department of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, Arizona (Butt, Smith, Tazelaar, Larsen).
From the Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota (Roden).
Arch Pathol Lab Med. 2022 May 1;147(5):525-533. doi: 10.5858/arpa.2021-0616-OA.
CONTEXT.—: Diffuse parenchymal lung disease (DPLD) is a well-recognized complication of systemic connective tissue disease (CTD) but rarely arises in patients with psoriasis or psoriatic arthritis, a poorly understood phenomenon.
OBJECTIVE.—: To characterize DPLD associated with psoriasis or psoriatic arthritis, with or without prior immunomodulation.
DESIGN.—: Pathology consultation files were searched for patients having psoriasis or psoriatic arthritis and DPLD. After excluding cases with active infection or smoking-related DPLD only, 44 patients (22 women; median age, 60 years; range, 23-81 years) were enrolled. Clinical history and pathology slides were reviewed.
RESULTS.—: Twenty-seven of 44 patients (61%) had psoriatic arthritis; the remainder had psoriasis alone. Most presented many years later with nonspecific respiratory symptoms. Nearly one-third had no prior immunosuppression, and most had no concomitant CTD. Radiographically, ground-glass opacities, consolidation, and/or reticulation were typical. Histologically, nonspecific interstitial pneumonia and unclassifiable fibrosis were seen in 24 patients (55%) and 8 patients (18%), respectively; usual interstitial pneumonia and airway-centered fibrosis were rare. Superimposed acute lung injury was common, usually manifesting as organizing pneumonia. Lymphoplasmacytic infiltrates, lymphoid aggregates, and chronic pleuritis were frequent. Interstitial granulomas were seen in 17 patients (39%) but were usually rare, poorly formed, and nonnecrotizing. No histologic differences were apparent among patients with or without concomitant CTDs or prior therapy.
CONCLUSIONS.—: Some patients with psoriasis or psoriatic arthritis develop clinically significant DPLD, even without prior therapy. Histopathologic findings mirror changes seen with other CTDs. Additional studies are warranted to clarify the association between psoriasis or psoriatic arthritis and DPLD.
弥漫性肺实质疾病(DPLD)是系统性结缔组织病(CTD)的一种公认并发症,但在患有银屑病或银屑病关节炎的患者中很少发生,这是一个尚未被充分理解的现象。
描述与银屑病或银屑病关节炎相关的 DPLD,无论是否存在先前的免疫调节治疗。
检索有银屑病或银屑病关节炎和 DPLD 的患者的病理会诊档案。在排除活动性感染或与吸烟相关的 DPLD 后,仅纳入 44 例患者(22 名女性;中位年龄 60 岁;范围 23-81 岁)。回顾临床病史和病理切片。
44 例患者中有 27 例(61%)患有银屑病关节炎;其余的仅有银屑病。大多数患者多年后出现非特异性呼吸系统症状。近三分之一的患者没有先前的免疫抑制治疗,大多数患者没有同时患有 CTD。影像学表现为磨玻璃影、实变和/或网状影。组织学上,24 例患者(55%)表现为非特异性间质性肺炎,8 例患者(18%)表现为无法分类的纤维化;寻常型间质性肺炎和气道中心性纤维化罕见。急性肺损伤重叠很常见,通常表现为机化性肺炎。淋巴浆细胞浸润、淋巴样聚集和慢性胸膜炎很常见。17 例患者(39%)存在间质肉芽肿,但通常数量较少、形态不规则且无坏死。无论患者是否同时患有 CTD 或是否存在先前的治疗,组织学表现均无明显差异。
一些患有银屑病或银屑病关节炎的患者会出现有临床意义的 DPLD,即使没有先前的治疗。组织病理学发现与其他 CTD 所见的变化相似。需要进一步研究来阐明银屑病或银屑病关节炎与 DPLD 之间的关联。