Primary Immunodeficiencies

49


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. 49.149.8); 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

Full access? Get Clinical Tree

Get Clinical Tree app for offline access