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diagnosis rheumatology hematology activation behcet differential disease erythematosus hemeonc hemophagocytic hlh lymphohistiocytosis muscle myopathy pathophysiology primary sams sarcoidosis sjogrens statin
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Syndrome (MAS) ... lupus erythematosus ... (CNS) dysfunction ... [SLE], AOSD) • ... #Management #Hematology
Primary Sjogren’s Syndrome: Pathogenesis and Clinical Findings • Primary Sjögren's is a solitary process whereas secondary Sjögren's
may be seen in ... (PBC), or with systemic ... lupus erythematosus ... (SLE) Signs / ... #Symptoms
SLE (Systemic Lupus Erythematosus) Suspect: Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
SLE (Systemic Lupus ... polyclinic or patchy papulosquamous ... CNS • Headache ... : • Symptoms limited ... #Systemic #Lupus
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
Systemic disease ... symptoms (headache ... Oral aphthae : SLE ... #diagnosis #management ... #signs #symptoms
Statin Induced Muscle Toxicity - Summary Clinical Presentation: • Elevations of serum creatine kinase with proximal myalgia
(GBS), systemic ... lupus erythematosus ... (SLE), polymyositis ... (LEMS), systemic ... myopathy #diagnosis #management
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
Diagnosis and Management ... dysregulation: activated macrophages ... mediators such as ... skin (16-32%): lupus ... #Signs #Symptoms
Vasculitis - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions • Mononeuritis multiplex • Hematuria, proteinuria,
SLE, atherosclerotic ... Symptoms (SX) in ... purpura: Strong sign ... • Progressive symptoms ... chorioretinitis, CNS
TAFRO TAFRO syndrome was first described in 2010, standing for: - Thrombocytopenia - Anasarca - Fever - Reticulin fibrosis - Organomegaly TAFRO syndrome
lupus erythematosus ... (SLE), Sjögren’ ... and the systemic ... symptoms Histopathological ... TAFRO #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
of the immune system ... (often termed MAS-HLH ... : Macrophage Activation ... Presentation • Common Signs ... and Symptoms:
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