Auszug
Die erste Beschreibung der Erkrankung geht auf Mikulicz im Jahr 1888 zurück. 1933 fasste der schwedische Ophthalmologe Henrik Sjögren in einer Monographie 19 Patienten mit typischer Keratoconjunctivitis sicca und Xerostomie sowie systemischen Manifestationen zusammen. Differenzial diagnostische Erfordernisse in der Einordnung einer Sicca-Symptomatik mit verbesserten Einstichten in die pathogenese und Möglichkeiten der Diagnostik haben wesentlich für die Erkennung des Sjögren-Syndroms und zur Abgrenzung einer Vielzahl von Erkrankungen ohne autoimmune Groundlage beigetragen.
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Dörner, T. et al. (2008). Sonstige Systembeteiligung des Bindegewebes (M 35). In: Zeidler, H., Zacher, J., Hiepe, F. (eds) Interdisziplinäre klinische Rheumatologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-34105-5_61
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