14 results
SLICC SLE Diagnostic Criteria - Systemic Lupus Erythematosus
Clinical and Immunologic Criteria

CLINICAL CRITERIA
 - ACUTE CUTANEOUS LUPUS
SLICC SLE Diagnostic ... Clinical and Immunologic ... Criteria CLINICAL ... #Diagnosis #Rheumatology ... #SLE #Lupus #Erythematosus
CNS Manifestations of Systemic Lupus Erythematosus (SLE)

Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
cause ischemia and ... vasculopathy, thrombosis and ... (@neudrawlogy) and ... #CNS #neurology ... #rheumatology #
Lupus is diagnosed using clinical and laboratory diagnostic criteria set by the American College of Rheumatology.
Lupus is diagnosed ... using clinical ... and laboratory diagnostic ... (SLE) requires ... #SLE #Lupus #Erythematosus
Drug Induced Lupus vs SLE
Drug Induced Lupus (DIL):
 • Epidemiology: -10% of all lupus cases, drug-dependent,
with PTU (50%) and ... weeks to months) and ... Lupusreference #druginduced ... #lupus #sle #comparison ... #table #rheumatology
EULAR/ACR Classification Criteria for Systemic Lupus Erythematosus
Clinical Domains:
 • Constitutional domain: Fever
 • Cutaneous domain: Non-scarring
Classification Criteria ... Erythematosus Clinical ... low C4, Low C3 and ... #SLE #Systemic ... #diagnosis #rheumatology
Management of Lupus Nephritis
Lupus nephritis (LN) in 10 to 40% of SLE
Hallmark = proteinuria 20.5 g/g
in 10 to 40% of SLE ... classification) and ... (NC) : active and ... (A/C) : active and ... #nephrology
SLE (Systemic Lupus Erythematosus)

Suspect:
Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
SLE (Systemic Lupus ... ) Suspect: Clinical ... findings (ANA, ... Non-autoimmune rheumatologic ... and CNS • Headache
Focal Hand Neuromyotonia 

Focal neuromyotonia in SLE.  A 42 year old with a 10 year
Focal Hand Neuromyotonia ... history of Systemic lupus ... of her left 4th and ... #clinical #video ... #neurology #physicalexam
Macrophage Activation Syndrome (MAS)
Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH)

What?
A subset of
, such as IL-1 and ... hemophagocytosis and ... nervous system (CNS ... • Heart, lung, and ... #Rheumatology
Behçet's Syndrome
Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy
Epidemiology:
 • Young
association • M > F Clinical ... Behcet syndrome (Clinical ... Oral aphthae : SLE ... • Arthritis: SLE ... signs #symptoms #rheumatology