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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

VASCULAR DISORDERS
Arteriosclerosis – tongue necrosis 
Oral Surg Oral Med Oral
Pathol 89:316–318, 2000
Necrotizing vasculitis in HIV 
Schweiz Monatsschr Zahnmed
105:54–62, 1995
Polyarteritis nodosa – tongue necrosis 
Acta Pediatr
84:1333–1336, 1995
TONGUE, ULCER
647
Schneiderman page 600-722.qxd 5/16/2006 6:51 PM Page 647


Temporal arteritis (giant cell arteritis) – ulcer progressing to
gangrene 
BJD 151:721–722, 2004; Oral Surg 74:582–586,
1992; Acta Med Scand 220:379–380, 1986; JAAD
6:1081–1088, 1982; BJD 76:299–308, 1964
Wegener’s granulomatosis 
Br J Clin Pract 46:268–269, 1992
TRANSIENT BLISTERS IN INFANTS
Congenital self-healing mechanobullous dermatosis
Perinatal trauma/iatrogenic injury 
Textbook of Neonatal
Dermatology, p.148, 2001
Self-limited forms of epidermolysis bullosa (Bart’s syndrome) 
Sucking blisters
Transient bullous dermolysis of the newborn
Transient maternal autoimmune blistering dermatosis
TRICHOMEGALY
Arch Ophthalmol 115:557–558, 1997; Principles and
Practice of Ophthalmol, p.1852, 1994; AD 123:1599–1601,
1987
Acrodynia
AIDS 
AIDS 17:1695–1696, 2003; J Eur Acad Dermatol
Venereol 11:89–91, 1998; Arch Ophthalmol 115:557–558,
1997; JAAD 28:513, 1993; AD 123:1599–1601, 1987
AIDS and alopecia areata 
Dermatology 193:52–53, 1996
Allergic diseases – children 
Ped Derm 21:534–537, 2004
Anorexia nervosa
Bimatoprost 
JAAD 51:S77–78, 2004
Cataract and spherocytosis 
Am J Ophthalmol 73:333–335, 1972
Coffin–Siris syndrome – autosomal recessive; hypertrichosis of
eyelashes, eyebrows, and lumbosacral areas 
JAAD
48:161–179, 2003
Cone-rod congenital amaurosis associated with congenital
hypertrichosis 
J Med Genet 26:504–510, 1989
Cornelia de Lange syndrome (Brachmann de Lange) –
trichomegaly, synophrys, low hairline, low birth weight, mental
deficiency, abnormal speech development, malformed upper
limbs 
Am J Med Genet 47:940–946, 1993; J Pediatr Ophthalmol
Strabismus 27:94–102, 1990; Syndromes of the Head and
Neck; Gorlin; 1990;p.300–304
Cyclosporin A 
Am J Ophthalmol 109:293–294, 1990
Dermatomyositis 
Dermatology 205:305, 2002
Drug-induced – benoxaprofen, corticosteroids, cyclosporine
Ann Ophthalmol 24:465–469, 1992; Nephrol Dial Transplant
11:1159–1161, 1996; diazoxide, interferon-
α
Lancet 359, 1107,
March, 2002; J Interferon Cytokine Res 20:633–634, 2000;
Eye 13:241–246, 1999; latanaprost Cutis 67:109–110, 2001;
Clin and Exp Ophthalmol 29:272–273, 2001; minoxidil,
penicillamine, phenytoin, psoralen, streptomycin, zidovudine
Familial trichomegaly 
Arch Ophthalmol 115:1602–1603, 1997
Gefitinib (epidermal growth factor receptor inhibitor) 
BJD
151:1111–1112, 2004; Acta Oncol 42:345–346, 2003
Hermansky–Pudlak syndrome 
AD 135:774–780, 1999
Hypertrichosis lanuginose, congenital 
Rook p.2890—2891,
1998, Sixth Edition; J Genet Humaine 17:10–13, 1969
Hypothyroidism
Interferon – interferon A 
NEJM 311:1259, 1984; interferon-
α
2B
Lancet 359:1107, 2002
Kabuki makeup syndrome 
J Pediatr 105:849–850, 1984
Liver disease, chronic
Leishmaniasis – Kala-azar (Pitaluga’s sign) 
Rook p.2994, 1998,
Sixth Edition
Lupus erythematosus, systemic 
Clin Rheumatol 19:245–246,
2000
Malnutrition
Metastatic adenocarcinoma 
Clin Exp Dermatol 20:237–239, 1995
Oliver–McFarlane syndrome – autosomal recessive;
trichomegaly, pigmentatary degeneration of retina, mental and
growth retardation, peripheral neuropathy, anterior pituitary
deficiencies 
Br J Ophthalmol 87:119–120, 2003; Can J
Ophthalmol 28:191–193, 1993; Genet Couns 2:115–118,
1991; Am J Med Genet 34:199–201, 1989; Am J Ophthalmol
101:490–491, 1986; Am J Dis Child 121:344–345, 1971;
Arch Ophthalmol 74:169–171, 1965
Phenylketonuria 
Rook p.2812, 2994, 1998, Sixth Edition
Porphyria
Pregnancy
Pretibial myxedema coma
Vitreochorioretinal degeneration 
Ann Ophthalmol 8:811–815,
1976

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