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diagnosis rheumatology dermatomyositis neck photo poikiloderma treatment activation adultonset aflp algorithm antimda5 antimda5dm antinxp2 antinxp2dm arteritis central civatte common cvid
Maculopapular Rashes - THE ALGORITHMIC APPROACH The term maculopapule is a portmanteau, a combination of macule and
macule and papule (Table ... febrile have a wide differential ... rashes but without signs ... have a broader differential ... #Diagnosis #Dermatology
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
infiltration) Differential ... Maternal Support - Critical ... Monitor and Treat Complications ... #Pregnancy #hepatology ... obgyn #diagnosis #management
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 ... , Schnitzler) Complications ... Disease #diagnosis #management
ANTI-MDA5 DERMATOMYOSITIS Cutaneous manifestations: • Periorbital heliotrope (blue-purple) rash with edema • Erythematous rash on the face, or the
(blue-purple) rash ... • Erythematous rash ... auricular papules Clinical ... Liver biopsies show ... #dermatology #diagnosis
Shawl sign poikiloderma in Dermatomyositis Poikiloderma in general is a common finding in older individuals with chronic
Shawl sign poikiloderma ... symptoms helps differentiate ... Dermatomyositis #Rash ... Dermatomyositis #Dermatology ... #Clinical #Photo
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... Diagnosis: HLH signs ... lymph node, or liver ... Lymphohistiocytosis #diagnosis #management ... #treatment #hematology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Fever is the main clinical ... Petechial or purpuric rash ... thrombocytopenia • Liver ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... noninfectious complications ... disease • Liver ... hypogammaglobulinemia #immunology #hematology ... #diagnosis #management
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
and ophthalmic complications ... Diagnosis = clinical ... systemic sx + signs ... very remarkable w/differential ... Symptoms #Diagnosis #Management
Monkeypox What? Monkeypox virus belongs to the family Poxviridae, subfamily Chordopoxvirinae, and genus orthopoxvirus Viral zoonotic disease that is
• Fomites • Live ... three weeks Clinical ... IgM antibody Complications ... MPOX #Diagnosis #Management ... #Dermatology
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