Primary Immunodeficiencies

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Primary Immunodeficiencies




• Heterogeneous group of disorders characterized by immune system defects that result in increased susceptibility to various infections, often with additional manifestations such as autoimmunity, allergy, and risk of malignancy.


• The genetic basis has been determined for >150 primary immunodeficiencies.


• Many immunodeficiency syndromes present with dermatologic findings that can facilitate early diagnosis (Table 49.1; Figs. 49.1–49.8); these features may be divided into three categories:


– Recurrent, severe, atypical or recalcitrant mucocutaneous infections, most often with Staphylococcus aureus, Candida spp., and human papillomaviruses.


– Patterns of cutaneous inflammation that are shared by several immunodeficiencies, e.g. eczematous dermatitis, non-infectious granulomas, lupus erythematosus-like lesions, small vessel vasculitis, and ulcers.


– More specific skin findings suggestive of particular disorders, e.g. oculocutaneous telangiectasias in ataxia telangiectasia and maternofetal GVHD in severe combined immunodeficiencies (SCID).







Apr 22, 2016 | Posted by in Dermatology | Comments Off on Primary Immunodeficiencies

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