Schneiderman Prelims Vol-I. qxd

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Schneiderman page 1-100.qxd 5/16/2006 6:49 PM Page 27

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Psoriasis 
BJD 149:1064–1066, 2003; JAAD 7:130–132, 1982
Raynaud’s phenomenon 
JAAD 44:381–384, 2001
Reynold’s syndrome – CREST syndrome and primary biliary
cirrhosis 
JAAD 44:381–384, 2001
Rheumatoid arthritis 
Rheumatologie 22:1–6, 1970
Sarcoidosis – mutilating form 
AD 133:882–888, 1997
Scleroderma (progressive systemic sclerosis) 
JAAD
44:381–384, 2001; linear scleroderma AD
132:1520–1521, 1996
Simonart syndrome 
Hautarzt 54:163–166, 2003
Syphilis, tertiary 
JAAD 44:381–384, 2001
Syringomyelia 
JAAD 44:381–384, 2001
Trauma 
JAAD 44:381–384, 2001
Vohwinkel’s syndrome (keratosis hereditarium mutilans) –
knuckle papules, palmoplantar keratoderma, ichthyosis,
pseudoainhum 
Clin Exp Dermatol 27:243–246, 2002; JAAD
44:376–378, 2001; Hautarzt 44:738–741, 1993
Warts – bone destruction of distal phalanx 
AD 107:275–276, 1973
ALOPECIA
N = non-scarring
S = scarring
AUTOIMMUNE DISEASES, AND DISEASES
OF IMMUNE DYSFUNCTION
Alopecia areata – associations with adrenal disease, atopy,
cytomegalovirus, Down’s syndrome, Hashimoto’s thyroiditis,
pernicious anemia, vitiligo 
Ghatan p.122, 2002, Second Edition
Rook p.2923–2925, 1998, Sixth Edition
APECED (polyendocrinopathy, candidiasis, ectodermal
dystrophy) syndrome 
Rook p.2743, 1998, Sixth Edition
Atrichia with severe T-cell immunodeficiency and nail dystrophy
Nature 398:473–474, 1999
Brunsting–Perry pemphigoid
Chronic mucocutaneous candidiasis 
NEJM 300:164–168,
1979; with dermatophytosis without endocrinopathy Rook
p.2744–2745, 1998, Sixth Edition
Cicatricial pemphigoid (S) 
Rook p.1874–1875, 1998, Sixth
Edition; AD 131:580–581, 1995; BJD 118:209–217, 1988; Oral
Surg 54:656–662, 1982
Dermatomyositis (NS or S) 
Epidermolysis bullosa acquisita 
AD 131:618–95, 1995
Fogo selvagem
Graft vs. host disease, chronic (S) 
JAAD 38:369–392, 1998
Immunodeficiency diseases (Wiskott–Aldrich syndrome,
immunoglobulin deficiency diseases, severe combined
immunodeficiency) – alopecia and dermatitis 
Ped Derm
16:95–102, 1999; combined immunodeficiency – desquamative
erythematous, morbilliform or vesiculopapular eruption of
newborn (3 weeks) with progressive alopecia 
Rook p.498–499,
1998, Sixth Edition; common variable immunodeficiency –
scarring alopecia with sarcoidal granulomas 
BJD 144:597–600,
2001; alopecia and infantile erythroderma – highly suggestive
of an immunodeficiency syndrome including Omenn syndrome
AD 136:875–880, 2000
IPEX syndrome – X-linked; immune dysregulation,
polyendocrinopathy, enteropathy; mutation of FOXP3;
nummular dermatitis, urticaria, scaly psoriasiform plaques of
trunk and extremities, penile rash, alopecia universalis, bullae
AD 140:466–472, 2004
Lupus erythematosus (LE) – systemic LE (NS or S) – diffuse,
patchy, or anterior with broken hairs (‘lupus hair’) 
Rook p.2475,
1998, Sixth Edition; subacute cutaneous lupus erythematosus –
non-scarring alopecia 
Med Clin North Am 73:1073–1090, 1989;
JAAD 19:1957–1062, 1988; bullous LE, discoid LE (S),
neonatal LE 
JAAD 50:25–32, 2004; Ped Derm 15:38–42, 1998
Morphea – including linear morphea (en coup de sabre)
Rook p.2504–2508,2936, 1998, Sixth Edition; pansclerotic
morphea 
JAAD 53:S115–119, 2005; – hypotrichosis Ped Derm
19:151–154, 2002
Pemphigus vulgaris
Scleroderma (S) 
Sjögren’s syndrome – patchy alopecia 
Ghatan p.174, 2002,
Second Edition, diffuse alopecia Rook p.2571, 1998, Sixth Edition