z-logo
open-access-imgOpen Access
Letters to the Editor: Refractory SAPHO syndrome with positive Th17-related pathway immunohistochemistry staining
Author(s) -
Shuo Zhang,
Chen Li,
Xiaohua Shi,
Wenrui Xu,
Mengchun Gong,
Wen Zhang,
Shuyang Zhang
Publication year - 2018
Publication title -
european journal of inflammation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.219
H-Index - 20
eISSN - 2058-7392
pISSN - 1721-727X
DOI - 10.1177/2058739218794058
Subject(s) - medicine , immunohistochemistry , pathology , rankl , sapho syndrome , synovitis , rheumatoid arthritis , receptor , activator (genetics) , pustulosis
A 34-year-old female was presented with left clavicle mass, recurrent ostalgia, and vesiculo-pustular rash in hands and feet. During 9 years of disease duration, she received first- and second-line therapies, however, with poor respond to non-steroidal anti-inflammatory drugs and disease-modifying antirheumatic drugs. Upon arrival, the physical examination revealed right clavicle swollen with severe tenderness and poor lumbar motility. Laboratory evaluation revealed elevated inflammatory indicators and imaging examinations revealed multiple bone erosion and sclerosis. The immunohistochemical staining of the bone biopsy presented the elevation of the Th17-related cytokines interleukin (IL)-6, IL-17, and IL-23, and negative expression of tumor necrosis factor (TNF)-β and receptor activator NK-κB ligand (RANKL). The immunohistochemical staining of target tissue revealed possible physiologic pathway and potential treatment target. Th17-related pathway might function as the central pathway of pathophysiologic process in SAPHO syndrome.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom