Schneiderman Prelims Vol-I. qxd

VASCULAR DISEASES
Eczematoid pigmented purpuric eruption
Port wine stain with overlying dermatitis 
BJD 144:1269–1270,
2001
Post-phlebitic syndrome – pain, edema, night cramps,
hemosiderin deposition, dermatitis 
Phlebology 11:2–5, 1996
Saphenous vein graft donor site dermatitis
Arch Surg 129:609,
1993
Vasculitis simulating eczematous dermatitis – with C
2
deficiency
Acta DV 67:265–7, 1987
Venous stasis dermatitis 
Rook p.659, 1998, Sixth Edition
DERMATITIS, FACIAL, PEDIATRIC
AUTOIMMUNE DISEASES, AND DISEASES
OF IMMUNE DYSFUNCTION
Allergic contact dermatitis
Bare lymphocyte syndrome 
Rook p.2745, 1998, Sixth Edition
Bruton’s hypogammaglobulinemia – atopic-like dermatitis;
dermatomyositis-like syndrome 
Rook p.2749, 1998, Sixth
Edition
C3 deficiency – recurrent infections, vasculitis, LE; C3
inactivator deficiency – dermatitis early in infancy 
Rook p.2744,
1998, Sixth Edition
Chronic granulomatous disease – X-linked or autosomal
recessive, seborrheic dermatitis-like changes, 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
DiGeorge’s syndrome (may be same as velocardiofacial
syndrome) – 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 
Rook p.498, 1998, Sixth Edition