Schneiderman Prelims Vol-I. qxd

PSYCHOCUTANEOUS DISEASES
Factitial panniculitis 
JAAD 45:325–361, 2001
SYNDROMES
Acute anterior tibial compartment syndrome – cellulitis-like
JAAD 34:521–522, 1996
Albright’s hereditary osteodystrophy
(pseudohypoparathyroidism) – osteomas
Ataxia telangiectasia – cutaneous granulomas present as
papules or nodules, red plaques with atrophy or ulceration;
telangiectasias of bulbar conjunctivae, tip of nose, ears,
antecubital and popliteal fossae, dorsal hands and feet; atrophy
with mottled hypo- and hyperpigmentation, dermatomal CALMs,
photosensitivity, canities, acanthosis nigricans, dermatitis 
AD
134:1145–1150, 1998; JAAD 10:431–438, 1984
Autoerythrocyte sensitization syndrome (painful bruising
syndrome) 
Ann DV 129:1029–1032, 2002
Buschke–Ollendorff syndrome
Epidermodysplasia verruciformis 
AD 131:1312–1318, 1995
Farber’s disease (disseminated lipogranulomatosis) – red
papules and nodules of joints and tendons of hands and feet;
deforming arthritis; papules, plaques, and nodules of ears, back
of scalp and trunk 
Rook p.2642, 1998, Sixth Edition; Am J Dis
Child 84:449–500, 1952
Familial eosinophilic cellulitis, short stature, dysmorphic habitus,
and mental retardation – bullae, vesicles, and red plaques
JAAD 38:919–928, 1998
Familial Hibernian fever – mimicking infectious cellulitis 
Ann
Intern Med 142:47–55, 2005; Q J Med 51:469–480, 1982
Familial Mediterranean fever – autosomal recessive; erysipelas-
like erythema – mutation in pyrin/marenostrin 
JAAD
42:791–795, 2000; AD 136:1487–1494, 2000; mimicking
infectious cellulitis 
Ann Intern Med 142:47–55, 2005; Isr Med
Assoc J 1:31–36, 1999; Q J Med 75:607–616, 1990
Glucagonoma syndrome – cellulitis-like 
Ann Intern Med
142:47–55, 2005
Goltz’s syndrome
Hypereosinophilic syndrome – urticarial plaque; red plaque
BJD 143:641–644, 2000; Sem Derm 14:122–128, 1995;
Blood 83:2759–2779, 1994; Medicine 54:1–27, 1975
Hyper-IgD syndrome 
AD 130:59–65, 1994
Infantile systemic hyalinosis – autosomal recessive; dusky red
plaques of buttocks, synophrys, thickened skin, perianal
nodules, gingival hypertrophy, joint contractures, juxta-articular
nodules (knuckle pads), osteopenia, growth failure, diarrhea,
frequent infections, facial red papules 
JAAD 50:S61–64, 2004
Kawasaki’s disease – mimicking periorbital cellulitis 
NEJM
350:904–912, 2004
KID syndrome – keratosis, ichthyosis, deafness syndrome –
fixed orange, symmetrical hyperkeratotic plaques of scalp, ears,
face, and extremities with perioral rugae; aged or leonine facies;
erythrokeratoderma-like; later hyperkeratotic nodules develop
Ped Derm 17:115–117, 2000; Ped Derm 13:105–113, 1996