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Dermatologic Differential Diagnosis.pdf. - Famona Site

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esponse element binding protein Ped Derm 21:44–47, 2004;<br />

JAAD 46:161–183, 2002; JAAD 46:159, 2002<br />

Sweet’s syndrome; with septal granulomatous or neutrophilic<br />

lobular panniculitis AD 121:785–788, 1985<br />

Thrombocytopenia-absent radius syndrome (TAR syndrome) –<br />

extensive proliferative hemangioma of the face<br />

Trichothiodystrophy syndromes – BIDS, IBIDS,<br />

PIBIDS – hemangiomas, sparse or absent eyelashes<br />

and eyebrows, brittle hair, premature aging,<br />

sexual immaturity, ichthyosis, dysmyelination,<br />

bird-like facies, dental caries; trichothiodystrophy with<br />

ichthyosis, urologic malformations, hypercalciuria and<br />

mental and physical retardation JAAD 44:891–920, 2001;<br />

Ped Derm 14:441–445, 1997<br />

Partial trisomy 2P – hemangiomas Rook p.2812, 1998,<br />

Sixth Edition<br />

Tuberous sclerosis – angiofibromas Syndromes of the Head<br />

and Neck, p.410–415, 1990<br />

Von Hippel–Lindau syndrome – hemangiomas Rook p.2710,<br />

1998, Sixth Edition<br />

X-linked hyper-IgM syndrome treated with G-CSF –<br />

disseminated pyogenic granulomas JAAD 49:105–108, 2003<br />

XXYY syndrome – features of Klinefelter’s; sparse body hair;<br />

also multiple angiomas, acrocyanosis, and premature peripheral<br />

vascular disease AD 94:695–698, 1966<br />

TRAUMA<br />

Chondrodermatitis nodularis chronicus helicis<br />

Fiddler’s neck JAAD 22:657–663, 1990<br />

Nose piercing with pyogenic granuloma Rook p.925, 1998,<br />

Sixth Edition<br />

Perniosis<br />

Picker’s papule<br />

Pseudo-Kaposi’s sarcoma in reflex sympathetic dystrophy JAAD<br />

22:513–520, 1990<br />

VASCULAR<br />

Acral pseudolymphomatous angiokeratoma of children<br />

(APACHE) – unilateral multiple persistent vascular papules<br />

on hands and feet; may have keratotic surface or collar<br />

JAAD 38:143–175, 1998; BJD 124:387–388, 1991; AD<br />

126:1524–1525, 1990<br />

Acroangiodermatitis of Mali JAAD 37:887–920, 1997;<br />

Int J Dermatol 33:179–183, 1994; due to A-V shunts<br />

JAAD 21:499–505, 1989; Arch Derm Res 281:35–39, 1989;<br />

AD 110:907, 1974; AD 111:1656, 1975; AD 100:297, 1969;<br />

associated with chronic venous insufficiency AD 96:176, 1967;<br />

AD 92:515, 1965<br />

Angiokeratoma – circumscriptum; angiokeratoma of Fordyce;<br />

Mibelli – acral vascular papules JAAD 45:764–766, 2001;<br />

solitary papular, of scrotum or vulva; angiokeratoma corporis<br />

diffusum (Fabry’s disease (α-galactosidase A) NEJM<br />

276:1163–1167, 1967; fucosidosis (α1-fucosidase) – autosomal<br />

recessive Rook p.2639, 1998, Sixth Edition; AD 107:754–757,<br />

1973; Kanzaki’s disease (α-N-acetylgalactosidase) – lesions on<br />

face and extremities AD 129:460–465, 1993; β-mannosidase<br />

deficiency; neuraminidase deficiency (sialidosis) Ghatan p.124,<br />

2002, Second Edition; aspartylglycosaminuria<br />

(aspartylglycosaminidase) Paediatr Acta 36:179–189, 1991;<br />

adult-onset GM1 gangliosidosis (β-galactosidase) Clin Genet<br />

17:21–26, 1980; galactosialidosis (combined β-galactosidase<br />

NODULES, RED OR VIOLACEOUS, WITH VASCULAR APPEARANCE 409<br />

and sialidase) AD 120:1344–1346, 1984; no enzyme<br />

deficiency AD 123:1125–1127, 1987; JAAD 12:885–886,<br />

1985) – telangiectasias or small angiokeratomas; and<br />

arteriovenous fistulae without metabolic disorders – papules<br />

AD 131:57–62, 1995<br />

Angiolymphoid hyperplasia with eosinophilia (Kimura’s disease) –<br />

papules and/or nodules along hairline AD 136:837–839, 2000;<br />

JAAD 38:143–175, 1998; JAAD 12:781–796, 1985<br />

Arteriovenous aneurysms<br />

Arteriovenous fistula with venous hypertension and<br />

pseudo-Kaposi’s sarcoma Rook p.2731, 1998, Sixth Edition;<br />

Clin Exp Dermatol 14:289–290, 1989<br />

Arteriovenous hemangioma (cirsoid aneurysm or acral<br />

arteriovenous tumor) – associated with chronic liver disease<br />

BJD 144:604–609, 2001<br />

Arteriovenous malformation<br />

Benign (reactive) angioendotheliomatosis (benign<br />

lymphangioendothelioma, acquired progressive lymphangioma,<br />

multifocal lymphangioendotheliomatosis) – present at birth; red<br />

brown or violaceous nodules or plaques on face, arms, legs with<br />

petechiae, ecchymoses, and small areas of necrosis<br />

AD 140:599–606, 2004; JAAD 38:143–175, 1998;<br />

AD 114:1512, 1978<br />

Bossed hemangioma with telangiectasia and peripheral pallor<br />

AD 134:1145–1150, 1998<br />

Cherry angiomas (Campbell de Morgan spots) Rook p.2092,<br />

1998, Sixth Edition<br />

Churg–Strauss disease<br />

Congenital infiltrating giant cell angioblastoma<br />

JAAD 37:887–920, 1997<br />

Congenital non-progressive hemangiomas – blue nodules<br />

AD 137:1607–1620, 2001<br />

Deep vein thrombosis<br />

Endovascular papillary angioendothelioma (Dabska’s tumor) –<br />

vascular nodule JAAD 38:143–175, 1998<br />

Epithelioid angiosarcoma – legs – resembles angiosarcoma<br />

JAAD 38:143–175, 1998<br />

Epithelioid hemangioendothelioma JAAD 20:362–366, 1989<br />

Eruptive pseudoangiomatosis – red papules Ped Derm<br />

19:243–245, 2002; BJD 143:435–438, 2000; JAAD 29:857–859,<br />

1993<br />

Erythema induratum<br />

Extravascular papillary angioendothelioma Ped Derm<br />

4:332–335, 1987<br />

Exuberant granulation tissue<br />

Familial cutaneo-cerebral capillary malformations –<br />

hyperkeratotic cutaneous vascular malformations Hum Mol<br />

Genet 9:1351–1355, 2000; Ann Neurol 45:250–254, 1999<br />

Familial multiple mucocutaneous venous malformations Hum<br />

Mol Genet 8:1279–1289, 199: Cell 87:1181–1190, 1996<br />

Glomangiomyoma – congenital multiple plaque-like<br />

glomangiomyoma Am J Dermatopathol 21:454–457, 1999<br />

Glomus tumor, solitary – painful pink, purple nodule Rook<br />

p.2357, 1998, Sixth Edition; multiple or plaque type; hemi-facial<br />

JAAD 45:239–245, 2001; Ped Derm 18:223–226, 2001;<br />

AD 127:1717–1722, 1991<br />

Hemangioendothelioma<br />

Hemangioma, proliferative, thrombosed; hemangioma of lower<br />

lateral cheek associated with airway obstruction; large facial<br />

hemangiomas of PHACES syndrome; sacral hemangiomas<br />

associated with spinal dysraphism; benign neonatal

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