Sjögren's syndrome in progressive systemic sclerosis (scleroderma)

Sicca features of Sjögren's syndrome were investigated in 25 consecutive patients with progressive systemic sclerosis by means of clinical examination, Schirmer's tests, rose bengal staining tests, secretory parotid sialographies, scintillation scanning of salivary glands with 99-mTc perte...

Full description

Saved in:
Bibliographic Details
Published inThe American journal of medicine Vol. 57; no. 1; pp. 78 - 85
Main Authors Alarcón-Segovia, Donato, Ibánez, Graciela, Hernández-Ortíz, Jorge, Velázquez-Forero, Francisco, González-Jiménez, Yolanda
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.1974
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Sicca features of Sjögren's syndrome were investigated in 25 consecutive patients with progressive systemic sclerosis by means of clinical examination, Schirmer's tests, rose bengal staining tests, secretory parotid sialographies, scintillation scanning of salivary glands with 99-mTc pertechnetate, radionuclide salivary excretion studies and lip biopsies for study of minor salivary glands. All 25 patients had at least one abnormal test and all but 3 patients had more than two abnormal tests. Pathologic findings in minor salivary glands included both lymphocytic infiltration and duct cell proliferation characteristic of Sjögren's syndrome, as well as collagen infiltration and disruption attributable to scleroderma. However, the finding of lacrimal and major salivary gland involvement indicates that Sjögren's syndrome does occur in the majority of patients with progressive systemic sclerosis. Because Sjögren's syndrome coexists almost exclusively with autoimmune disorders, our findings support the contention that progressive systemic sclerosis is related to autoimmunity.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0002-9343
1555-7162
DOI:10.1016/0002-9343(74)90771-2