Pacheco-Tena César, Pérez-Tamayo Ruy, Pineda Carlos, González-Chávez Susana A, Quiñonez-Flores Celia, Ugalde Vitelly Antonio, Inman Robert D, Aubin Jane E, Vázquez-Mellado Janitzia, Burgos-Vargas Rubén
From the Facultad de Medicina, Universidad Autónoma de Chihuahua, Chihuahua; Unidad de Medicina Experimental, Facultad de Medicina, Universidad Nacional Autónoma de México; Instituto Nacional de Rehabilitación; Servicio de Cirugía Plástica y Reconstructiva, and Servicio de Reumatología, Hospital General de México, México D.F., México; Arthritis Centre for Excellence, Toronto Western Hospital, and Department of Molecular Genetics University of Toronto, Toronto, Ontario, Canada.C. Pacheco-Tena, MD; S.A. González-Chávez, MSc; C. Quiñonez-Flores, MSc, Facultad de Medicina, Universidad Autónoma de Chihuahua; R. Pérez-Tamayo, MD, Unidad de Medicina Experimental, Facultad de Medicina, Universidad Nacional Autónoma de México; C. Pineda, MD, Dirección de Investigación, Instituto Nacional de Rehabilitación; A. Ugalde Vitelly, MD, Servicio de Cirugía Plástica y Reconstructiva, Hospital General de México; J. Vázquez-Mellado, PhD; R. Burgos-Vargas, MD, Servicio de Reumatología, Hospital General de México, Facultad de Medicina, Universidad Nacional Autónoma de México; R.D. Inman, MD, Arthritis Centre for Excellence, Toronto Western Hospital; J.E. Aubin, PhD, Department of Molecular Genetics, University of Toronto.
J Rheumatol. 2015 Apr;42(4):630-7. doi: 10.3899/jrheum.140218. Epub 2014 Dec 15.
Patients with juvenile-onset spondyloarthritis (SpA) may develop ankylosis of the midfoot resembling the spinal changes seen in patients with ankylosing spondylitis (AS). The study of the histopathology of the feet of patients with tarsitis could help us understand the pathogenesis of bone formation in affected structures in the SpA. The objective of our study was to describe the histopathologic characteristics of the midfoot in patients with tarsitis associated with SpA.
We obtained synovial sheaths, entheses, and bone samples from 20 patients with SpA with midfoot pain/tenderness and swelling. Tissue samples underwent H&E staining; immunohistochemistry for CD3, CD4, CD8, CD68, and CD20 cell identification; and immunofluorescence for bone lineage proteins, including osteocalcin, osteopontin, parathyroid hormone-related protein, bone sialoprotein, and alkaline phosphatase.
Slight edema and hyalinization were found in some tendon sheaths, and few inflammatory cells were detected in the entheses. In bones, we found some changes suggesting osteoproliferation, including endochondral and intramembranous ossification, but no inflammatory cells. In entheses showing bone proliferation, we detected osteocalcin and osteopontin in cells with a fibroblast-mesenchymal phenotype, suggesting the induction of entheseal cells toward an osteoblast phenotype.
Osteoproliferation and abnormal expression of bone lineage proteins, but no inflammatory infiltration, characterize midfoot involvement in patients with SpA. In this sense, tarsitis (or ankylosing tarsitis) resembles the involvement of the spine in patients with AS. Ossification may be in part explained by the differentiation of mesenchymal entheseal cells toward the osteoblastic lineage.
青少年起病的脊柱关节炎(SpA)患者可能会出现中足关节强直,类似于强直性脊柱炎(AS)患者的脊柱改变。研究跗骨炎患者足部的组织病理学有助于我们理解SpA中受累结构骨形成的发病机制。我们研究的目的是描述与SpA相关的跗骨炎患者中足的组织病理学特征。
我们从20例有中足疼痛/压痛及肿胀的SpA患者中获取滑膜鞘、附着点及骨样本。组织样本进行苏木精-伊红(H&E)染色;进行免疫组化以鉴定CD3、CD4、CD8、CD68和CD20细胞;进行免疫荧光检测骨系蛋白,包括骨钙素、骨桥蛋白、甲状旁腺激素相关蛋白、骨唾液蛋白和碱性磷酸酶。
在一些腱鞘中发现轻微水肿和玻璃样变,在附着点检测到少量炎症细胞。在骨骼中,我们发现一些提示骨增殖的改变,包括软骨内成骨和膜内成骨,但未发现炎症细胞。在显示骨增殖的附着点中,我们在具有成纤维细胞-间充质表型的细胞中检测到骨钙素和骨桥蛋白,提示附着点细胞向成骨细胞表型的诱导。
骨增殖和骨系蛋白的异常表达,但无炎症浸润,是SpA患者中足受累的特征。从这个意义上说,跗骨炎(或强直性跗骨炎)类似于AS患者的脊柱受累情况。骨化可能部分是由于间充质附着点细胞向成骨细胞系的分化所致。