DERMATITIS
AUTOIMMUNE DISEASES, AND DISEASES
OF IMMUNE DYSFUNCTION
Agammaglobulinemia
Curr Prob Derm 10:41–92, 1998;
J Allergy 33:406–411, 1962; X-linked hypogammaglobulinemia
(agammaglobulinemia)
J Allergy 33:406–411, 1962
Allergic contact dermatitis – numerous allergens
Rook
pp.733–819, 1998, Sixth Edition; plants Rook p.788, 1998,
Sixth Edition; woods Rook p.794, 1998, Sixth Edition; implanted
alloys
Rook p.771, 1998, Sixth Edition; ingested antibiotics after
topical sensitization (systemic eczematous contact dermatitis)
Contact Dermatitis 1:187, 1975; Acta DV 49:422–426, 1969;
lichens (woodcutters dermatitis)
Rook p.794–795, 1998, Sixth
Edition; p-phenylenediamine in color developers – lichenoid or
eczematous dermatitis
BJD 115:23–31, 1986; Contact
Dermatitis 10:280–285, 1984; complicating venous stasis Rook
p.2261, 1998, Sixth Edition; nail polish – generalized dermatitis
Contact Dermatitis 34:140–141, 1996; acrylic nails – dorsal
fingers
Rook p.2867, 1998, Sixth Edition; fingertip dermatitis –
garlic, tulips,
Alstroemeria; airborne contact dermatitis to
sesquiterpene lactones
Bolognia p.260, 2004; nickel allergic
contact dermatitis to school chairs with dermatitis of the upper
posterior thighs in girls
Cutis 74:27–28, 2004; hand and/or foot
dermatitis due to nickel in dental appliances
Contact Dermatitis
27:259–260, 1992
Anti-synthetase syndrome – mechanics’ hands, Raynaud’s
phenomenon, interstitial lung disease, anti-Jo-1 antibody
AD 141:779–784, 2005
Autoimmune estrogen dermatitis
JAAD 32:25–31, 1995
Autoimmune progesterone dermatitis
Acta DV 69:308–310, 1989
Bare lymphocyte syndrome
Rook p.2745, 1998, Sixth Edition
Bruton’s hypogammaglobulinemia – atopic-like dermatitis;
dermatomyositis-like syndrome
Rook p.2749, 1998, Sixth Edition
Bullous pemphigoid – eczematous lesions
JAAD 29:293–299,
1993; subacute prurigo variant JAAD 47:133–136, 2002
C3 deficiency – recurrent infections, vasculitis, LE; C3
inactivator deficiency – dermatitis early in infancy
Rook p.2744,
1998, Sixth Edition
Cell-associated glycoprotein deficiency
Chronic granulomatous disease – seborrheic dermatitis-like
changes, X-linked or autosomal recessive, Xp21 (distal end of
Xp), localized pyodermas, abscesses, granulomas, perioral and
intraoral ulcers, lungs/liver/spleen, defect in NADPH oxidase
system; including NADPH, phagocyte cytochrome b, and
cytosolic proteins; membrane-associate NADPH oxidase
system fails to produce superoxide and other toxic oxygen
metabolites;
Staphylococcus aureus, Klebsiella, Pseudomonas,
Escherichia coli, Serratia, Aspergillus, Candida, Cryptococcus,
Nocardia
Cicatricial pemphigoid
Dermatitis herpetiformis
Caputo p.24, 2000; dermatitis with or
without lichenification
Rook p.1890, Sixth Edition
Dermatomyositis
Bolognia p.210, 2004
DiGeorge’s syndrome (congenital thymic aplasia) – autosomal
dominant or sporadic; seborrheic dermatitis, atopic dermatitis;
developmental defects of 3rd and 4th pharyngeal pouches,
congenital thymic aplasia, neonatal tetany due to absence of
parathyroids, cardiac anomalies (truncus arteriosus), short
philtrum, low-set malformed ears, hypertelorism, increased
susceptibility to
Candida, viral and Pneumocystis carinii
infections, loss of portion of proximal long arm of chromosome
22, may be the same as velocardiofacial syndrome
Rook p.498,
1998, Sixth Edition
Fogo selvagem
Graft vs. host disease, chronic – lichenoid dermatitis
AD
119:683–689, 1983
Immunodeficiency diseases (Wiskott–Aldrich syndrome,
immunoglobulin deficiency diseases, severe
combined immunodeficiency) – alopecia and dermatitis
Ped Derm 16:95–102, 1999
X-linked immunodeficiency with hyper-IgM – atopic dermatitis-
like rash
Rook p.2749, 1998, Sixth Edition
Immunologic amnesia syndrome
NEJM 281:285–290, 1969
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