## Abstract Serum eosinophil chemotactic activity was determined by the Boyden chamber technique in 20 patients with eosinophilic fasciitis. Increased eosinophil chemotactic activity (>125% of background) was found in all 20 patients (mean 297% Β± 129), whereas sera of 20 controls with systemic scle
Capillary Microscopy in Eosinophilic Fasciitis
β Scribed by Michael B. Rozboril; Hildegard R. Maricq; Gerald P. Rodnan; Stephania Jablonska; Giles G. Bole
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 504 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
β¦ Synopsis
Capillary microscopy was performed on 19 patients with eoslnophilic fasciitis. These patients were compared with 13 individuals with progressive systemic sclerosis (scleroderma). Capillary patterns were normal in 16 of 19 (84%) eosinophilic fasciitis patients; 3 exhibited either borderline or nonspecific changes, and none showed a definite scleroderma pattern. In contrast, characteristic nailfold capillary changes, consisting of both dilatation and loss of capillaries, were present in 11 of 13 (85%) scleroderrna patients; the remaining 2 showed scleroderma-type abnormalities of only 1 finger and were, therefore, classified as borderline. These results suggest that capillary microscopy may help to distinguish these 2 disorders.
π SIMILAR VOLUMES
## Abstract Serum immune complexes were measured in 22 patients with eosinophilic fasciitis, 8 of whom had serial determinations. Elevated levels were found by Raji cell radioimmunoassay in 14 (64%) patients, by agarose gel electrophoresis in 13 (59%), and by C1q agglutinationβinhibition in 9 (41%)