Schneiderman Prelims Vol-I. qxd


PRIMARY CUTANEOUS DISEASE



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[Encyclopedia of Differential Diagnosis in Dermatology] Paul Schneiderman, Marc E. Grossman - A Clinician\'s Guide to Dermatologic Differential Diagnosis, Volume 1 The Text (Encyclopedia of Differential Diagnosis in D

PRIMARY CUTANEOUS DISEASE
Acanthosis nigricans 
Syndromes of the Head and Neck,
p.355, 1990
Angiolymphoid hyperplasia 
JAAD 11:333–339, 1984
Crenated tongue
TONGUE, MULTILOBULATED
643
Schneiderman page 600-722.qxd 5/16/2006 6:51 PM Page 643


Darier’s disease
Fissured tongue
Hypertrophy of circumvallate, foliate, or fungiform papillae
TRAUMA
Tension, scalloped tongue 
JAAD 15:1289, 1986
SYNDROMES
Blue rubber bleb nevus syndrome
Cowden’s syndrome – scrotal tongue 
JAAD 11:1127–1141, 1984
Down’s syndrome – scrotal tongue 
Rook p.3123, 1998,
Sixth Edition
Epidermal nevus syndrome
Focal epithelial hyperplasia (Heck’s disease) 
BJD 96:375–380,
1977
Gardner’s syndrome – multiple fibrous tumors
Goltz’s syndrome
LAMB syndrome – myxoma 
JAAD 10:72–82, 1984
Maffucci’s syndrome – multiple hemangiomas 
BJD 99
(Suppl 16):31–33, 1978; J Bone Jt Surg 55A:1465–1479, 1973
Melkersson–Rosenthal syndrome – scrotal tongue; orofacial
edema; edema of cheeks, forehead, eyelids, scalp
Oral Surg
Oral Med Oral Pathol 75:220–224, 1993; Oral Surg Oral Med
Oral Pathol 74:610–619, 1992; JAAD 21:1263–1270, 1989
Multicentric reticulohistiocytosis 
JAAD 20:530–532,535–536,
1989; Oral Surg Oral Med Oral Pathol 65:721–725, 1988
Multiple mucosal neuroma syndrome (MEN IIB) (Gorlin’s
syndrome) – skin-colored papules and nodules of lips, tongue,
oral mucosa 
AD 139:1647–1652, 2003; JAAD 36:296–300,
1997; Oral Surg 51:516–523, 1981; J Pediatr 86:77–83, 1975;
Am J Med 31:163–166, 1961
Neurofibromatosis 
Syndromes of the Head and Neck, p.395, 1990
Nevus sebaceous syndrome (Schimmelpenning–Feuerstein–
Mims syndrome) – papillomas of tongue, gingival hyperplasia,
thickened mucosa, anodontia, dysodontia 
JAAD 52:S62–64,
2005; Ped Derm 13:22–24, 1996; Int J Oral Maxillofac Surg
12:437–443, 1983
Oral–facial–digital syndrome type I (Papillon–Leage syndrome) –
X-linked dominant; short upper lip, hypoplastic alanasi, hooked
pug nose, hypertrophied labial frenulae, bifid or multilobed
tongue with small tumors within clefts, clefting of hard and soft
palate, teeth widely spaced, trident hand or brachydactyly,
syndactyly, or polydactyly; hair dry and brittle, alopecic,
numerous milia of face, ears, backs of hands, mental retardation
Ped Derm 9:52–56, 1992
Oral–facial–digital syndrome type II – autosomal recessive;
lobulated, bifid tongue; poly-, syn- and brachydactyly, cleft
palate, broad bifid nasal tip 
Clin Genet 2:261–266, 1971
Oral–facial–digital syndrome type III – lobulated hamartomatous
tongue, mental retardation, eye abnormalities, dental
abnormalities, bifid uvula, skeletal anomalies 
Clin Genet
2:248–254, 1971
Pachyonychia congenita – scrotal tongue
Sjögren’s syndrome – scrotal tongue
Werdnig–Hoffmann spinal muscular atrophy

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