15 results
diagnosis rheumatology dermatology disease lupus photo druginduced henoch hsp physicalexam purpura schonlein signs sle symptoms adultonset algorithm arteritis behcet causes
Causes of Petechial Rash - Differential Diagnosis Algorithm Pinpoint areas (less than 2 mm) of hemorrhage, which
- Differential ... Infection - Vasculitis ... Vasculitis (lupus ... deficiency Work ... #Differential #
Palpable Purpura seen in Henoch Schonlein Purpura (HSP, IgA Vasculitis) 55 year old male on tuberculosis treatment
Purpura (HSP, IgA Vasculitis ... on tuberculosis treatment ... rash. ... #clinical #photo ... #dermatology #skin
Dermatologic Manifestations of Granulomatosis with Polyangiitis (GPA) Skin involvement in granulomatosis with polyangiitis (GPA) is common and
Rarely dominate the clinical ... • Petechiae, Palpable ... Maculopapular rash ... reticularis Differential ... #rash #diagnosis
Henoch Schonlein Leg Rash - Palpable Purpura Purpura: Low Platelets or Vasculitis? 45 years old, seen in our
Schonlein Leg Rash ... Tip: To differentiate ... Palpable = vasculitis ... #clinical #photo ... #dermatology #HSP
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
40, F:M 9:1 • Clinical ... Manifestations: Malar rash ... • Immunologic Workup ... life-threatening • Treatment ... #Summary #rheumatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... arthritis, Skin rash ... fraction < 20% Differential ... Disease #diagnosis #management ... #treatment #rheumatology
Drug Induced Lupus vs SLE Drug Induced Lupus (DIL): • Epidemiology: -10% of all lupus cases, drug-dependent,
to 1:1 F:M • Clinical ... NPSLE rare, Malar rash ... • Immunologic Workup ... 40, F:M 9:1 • Clinical ... • Immunologic Workup
IgG4-Related Disease Clinical history: Man, 60 years, multiorgan involvement, unique or multiple inflammatory pseudotumor 4 phenotypes: •
Related Disease Clinical ... No necrosis, No vasculitis ... Disease #diagnosis #management ... #phenotypes #workup ... #treatment #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 ... multiforme-like lesions, palpable ... Behcet disease) Differential ... Arthritis, AS Treatment ... Syndrome #diagnosis #management
Pulmonary Renal Syndromes - OnePager Summary Autoimmune ANCA vasculitis (AAV): GPA (granulomatous with polyangiitis), EGPA (eosinophilic granulomatosis
Autoimmune ANCA vasculitis ... • Cutaneous: palpable ... mononeuritis multiplex WORKUP ... #diagnosis #management ... #treatment
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