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Livedo Reticularis and Livedo Racemosa

Livedo reticularis produces a mottled, purplish discoloration of the skin with reticulated cyanotic areas surrounding paler central cores (Figure 1–7ck). This distinctive “fishnet” pattern is

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IgG4-Related Disease

IgG4-related disease is a systemic disorder of unknown cause marked by highly characteristic fibroinflammation that contains IgG4 plasma cells and can infiltrate virtually any organ.

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Sjögren Syndrome

Sjögren syndrome is a systemic autoimmune disorder whose clinical presentation is usually dominated by dryness of the eyes and mouth due to immune-mediated dysfunction of

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Immune-Mediated Inflammatory Myopathies

Immune-mediated inflammatory myopathies include polymyositis, dermatomyositis, myositis resulting from a rheumatic disease or overlap syndrome, inclusion body myositis (IBM), and immune-mediated necrotizing myopathy. These disorders

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Raynaud Phenomenon

Raynaud phenomenon (RP) is a syndrome of paroxysmal digital ischemia, most commonly caused by an exaggerated response of digital arterioles to cold or emotional stress.

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Antiphospholipid Syndrome

The clinical features of primary antiphospholipid syndrome (APS) are venous or arterial occlusions or certain pregnancy complications. Laboratory criteria include the identification of at least

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Drug-Induced Lupus

Drug-induced lupus shares several clinical and serologic features with SLE but is due to ongoing exposure to a drug and resolves when the offending drug

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Systemic Lupus Erythematosus

SLE is an inflammatory autoimmune disorder characterized by autoantibodies to nuclear antigens. It can affect multiple organ systems. Many of its clinical manifestations are secondary

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Adult Still Disease

Still disease is a systemic form of juvenile chronic arthritis in which high spiking fevers are much more prominent, especially at the outset, than arthritis.

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