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  Vol. 126 No. 5, May 1990 TABLE OF CONTENTS
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Eosinophilic Fasciitis

Increased Collagen Production and Type I Procollagen Messenger RNA Levels in Fibroblasts Cultured From Involved Skin

Veli-Matti Kähäri, MD, PhD; Jyrki Heino, MD, PhD; Leo Niskanen, MD; Jorma Fräki, MD, PhD; Jouni Uitto, MD, PhD

Arch Dermatol. 1990;126(5):613-617.


Abstract

• Two patients with eosinophilic fasciitis were studied to elucidate the activation of collagen production in this disorder. Histologic examination of biopsy specimens from the involved area of skin revealed the presence of inflammatory cell infiltrates and various degrees of collagen accumulation in the dermis, subcutis, fascia, and underlying muscle. Fibroblast cultures initiated from the involved skin exhibited 2.0- to 3.7-fold increased collagen production when compared with control fibroblast cultures established from the uninvolved skin of the same patients. Eosinophilic fasciitis fibroblasts also displayed 2.4- to 6.2-fold higher steady-state levels of type I procollagen messenger RNA than did the control cells, indicating pretranslational activation of type I procollagen gene expression. In addition, cellular fibronectin messenger RNA steady-state levels were elevated 1.9- to 3.3-fold in eosinophilic fasciitis fibroblasts. These results suggest that fibroblasts in the involved skin of patients with eosinophilic fasciitis exhibit an activated phenotype, similar to that of scleroderma fibroblasts, leading to accumulation of collagen in the skin and the underlying structures.

(Arch Dermatol. 1990;126:613-617)



Author Affiliations

From the Departments of Dermatology and Biochemistry and Molecular Biology, Jefferson Medical College, Philadelphia, Pa (Drs Kähäri and Uitto); the Department of Medical Biochemistry, University of Turku (Finland) (Dr Heino); and the Departments of Internal Medicine (Dr Niskanen) and Dermatology (Dr Fräki), University of Kuopio (Finland).


Footnotes

Accepted for publication January 14, 1990.

Presented, in part, at the annual meeting of the Society for Investigative Dermatology, Washington, DC, April 27, 1989, and published in abstract form (Kähäri V-M, Heino J, Niskanen L, Fräki J, Uitto J. J Invest Dermatol. 1989;92:454).

Reprint requests to Department of Dermatology, Thomas Jefferson University, 1020 Locust St, Philadelphia, PA 19107 (Dr Kähäri).



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