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Vocabulary practice cards covering the general characteristics of collagenoses, Systemic Lupus Erythematosus (SLE), and Systemic Sclerosis based on lecture notes.
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Kollagenosen
Autoimmune diseases that affect connective tissue and where organ involvement is in the foreground.
UCTD
Undifferenzierte Kollagenose (Undifferentiated Connective Tissue Disease).
Overlap-Syndrom
Mixed clinical pictures (Mischbilder) comprising features of different autoimmune diseases.
ANA
Anti-Nukleäre Antikörper (Anti-Nuclear Antibodies), which are positive in collagenoses and specifically 95−100% positive in SLE.
Raynaud-Syndrom
A common symptom in systemic autoimmune diseases involving vascular spasms; it occurs in 90% of systemic sclerosis cases.
Sicca-Syndrom
A condition characterized by dryness of the eyes and mouth.
Hypergammaglobulinämie
An increase in gamma globulins reflecting B-cell hyperactivity.
Systemischer Lupus erythematodes (SLE)
An episodic autoimmune systemic disease with immunological hyperactivity and loss of tolerance against nuclear antigens.
Hypokomplementämie
The lowering or consumption of complement factors C3 and C4, often observed in SLE.
Schmetterlingserythem
Butterfly rash; a characteristic skin manifestation of Systemic Lupus Erythematosus.
Pannikulitis
Inflammation of the subcutaneous fatty tissue.
Lupusnephritis
Glomerulonephritis associated with SLE, classified into histological classes I-VI.
EULAR Klassifikationskriterien
Criteria used for the classification of SLE, where a score of >10 points is required.
Systemische Sklerose
A disease characterized by the triad of vasculitis (vaskulopathie), inflammation/autoimmunity, and fibrosis.
lcSSC
Limitierte systemische Sklerose; features sclerodactyly and skin involvement distal to the elbows.
dcSSC
Diffuse systemische Sklerose; features skin involvement proximal to the elbows and on the trunk (Stammbetont).
Sklerodaktylie
Hardening and tightening of the skin on the fingers, a symptom of systemic sclerosis.