Schneiderman Prelims Vol-I. qxd

NEOPLASTIC DISEASES
Familial hyperplasia of the pineal body
Linear epidermal nevus 
BJD 95:433–436, 1976
Lymphoma – lesions of CTCL simulating acanthosis nigricans
Am J Dermatopath 7:367–371, 1985
Melanocytic nevi – giant melanocytic lesions – acanthosis
nigricans-like changes
Parapsoriasis en plaque 
Ann Dermatol Venereol 118:23–26,
1991
PARANEOPLASTIC DISORDERS
Adenocarcinoma of breast, lung, colon, esophagus,
gallbladder, kidney, liver, ovary, pancreas, prostate,
rectum, uterus, gastrointestinal tract 
Ghatan p.121, 2002,
Second Edition
APUDomas 
Ghatan p.121 , 2002, Second Edition
Leser–Trelat 
JAAD 42:357–362, 2000
PRIMARY CUTANEOUS DISEASES
Acanthosis nigricans, benign – sporadic, familial (autosomal
dominant) 
Int J Dermatol 35:126–127, 1996; J R Soc Med
87:169, 1994; benign generalized Ped Derm 21:277–279, 2004;
Ped Derm 20:254–256, 2003; malignant – gastrointestinal
malignancies, especially gastric carcinoma; rarely lymphoma
JAAD 31:1–19, 1994
Atopic dermatitis – acanthosis nigricans-like changes
Bullous congenital ichthyosiform erythroderma (epidermolytic
hyperkeratosis) – acanthosis nigricans-like changes
Confluent and reticulated papillomatosis 
AD 129:961–963, 1993
Granular parakeratosis
Ped Derm 20:215–220, 2003
Ichthyosis hystrix – acanthosis nigricans-like changes
Unilateral acanthosis nigricans
SYNDROMES
Acral hypertrophy syndrome
Adrenogenital syndrome
Alström’s syndrome – retinitis pigmentosa, sensorineural
deafness, obesity, diabetes mellitus 
BJD 147:1096–1011, 2002;
Acta Paediatr Taiwan 41:270–272, 2000; Hum Mol Genet
6:213–219, 1997
Ataxia-telangiectasia 
JAAD 10:431–438, 1984
Bannayan–Riley–Ruvalcaba–Zonana syndrome (PTEN
phosphatase and tensin homolog hamartoma) – dolicocephaly,
frontal bossing, macrocephaly, ocular hypertelorism, long