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328 A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1<br />

Gout<br />

Median nerve injury<br />

Osteoid osteoma Rook p.2847, 1998, Sixth Edition<br />

Sarcoid<br />

Trauma<br />

Unilateral<br />

Aneurysm – left innominate artery<br />

Axillary Pancoast tumors<br />

Brachial arteriovenous aneurysm<br />

Patent ductus arteriosus with pulmonary hypertension<br />

Prolonged hemiplegia<br />

Bronchogenic carcinoma<br />

Bronchiectasis, cysts<br />

Carcinoma of the nasopharynx, colon, esophagus, stomach<br />

Ghatan p.79, 2002, Second Edition<br />

Celiac sprue JAAD 52:1020–1028, 2005<br />

CINCA syndrome JAAD 52:1020–1028, 2005<br />

Cirrhosis<br />

Crohn’s disease<br />

Congestive heart failure<br />

Cyanotic congenital heart disease<br />

JAAD 52:1020–1028, 2005<br />

Cystic fibrosis JAAD 52:1020–1028, 2005<br />

Diarrhea, chronic<br />

Down’s syndrome<br />

Familial<br />

Hemochromatosis<br />

Hereditary – autosomal dominant<br />

Hereditary mucoepithelial dysplasia<br />

HIV disease JAAD 52:1020–1028, 2005<br />

Hyperparathyroidism<br />

Hypertrophic osteoarthropathy<br />

Hypersensitivity pneumonitis JAAD 52:1020–1028, 2005<br />

Hypervitaminosis A<br />

Idiopathic<br />

Idiopathic pulmonary fibrosis JAAD 52:1020–1028, 2005<br />

Infective endocarditis JAAD 52:1020–1028, 2005<br />

Inflammatory bowel disease JAAD 52:1020–1028, 2005<br />

Juvenile polyposis coli JAAD 52:1020–1028, 2005<br />

Laxative abuse SMJ 76:1071, 1983; Lancet 2:947, 1978<br />

Liver disease JAAD 52:1020–1028, 2005<br />

Lung abscess, empyema<br />

Lupus erythematosus BJD 89:533–535, 1973<br />

Lymphoma JAAD 52:1020–1028, 2005<br />

Malabsorption<br />

Malaria<br />

Malnutrition Ghatan p.79, 2002, Second Edition<br />

Marfan’s syndrome – pseudoclubbing<br />

Myxedema, Graves’ disease (thyroid acropachy) Med Clin<br />

North Am 52:393–395, 1968<br />

Marie–Bamberger syndrome<br />

Mesothelioma JAAD 52:1020–1028, 2005<br />

Nasopharyngeal carcinoma JAAD 52:1020–1028, 2005<br />

Parasitic bacillary dysentery JAAD 52:1020–1028, 2005<br />

Phosphorus toxicity<br />

Pleural tumors JAAD 52:1020–1028, 2005<br />

POEMS syndrome JAAD 52:1020–1028, 2005<br />

Polycythemia<br />

Psoriatic onycho-pachydermoperiostitis BJD 143:901–902,<br />

2000; Rev Rheum Mal Osteoartic 56:579–582, 1989<br />

Pulmonary arteriovenous malformation JAAD<br />

52:1020–1028, 2005<br />

Pycnodysostosis – pseudoclubbing (acro-osteolysis) Br Med<br />

J iii:712–714, 1967<br />

Sarcoidosis JAAD 52:1020–1028, 2005<br />

Sprue<br />

Subacute bacterial endocarditis<br />

Syringomyelia<br />

Systemic lupus erythematosus<br />

Thymoma, malignant<br />

Thyroid disease JAAD 52:1020–1028, 2005<br />

Tuberculosis JAAD 52:1020–1028, 2005<br />

Ulcerative colitis<br />

Venous stasis JAAD 52:1020–1028, 2005<br />

X-linked reticulate pigmentary disorder with<br />

systemic manifestations (familial cutaneous amyloidosis)<br />

(Partington syndrome II) – X-linked; rare; Xp21–22; boys<br />

with generalized reticulated muddy brown pigmentation<br />

(dyschromatosis) with hypopigmented corneal<br />

dystrophy (dyskeratosis), coarse unruly hair,<br />

unswept eyebrows, silvery hair, hypohidrosis, recurrent<br />

pneumonia with chronic obstructive disease, clubbing;<br />

failure to thrive, female carriers with linear macular nevoid<br />

Blascko-esque hyperpigmentation Ped Derm 22:122–126,<br />

2005; Semin Cut Med Surg 16:72–80, 1997;<br />

Am J Med Gen 10:65:1981<br />

Gout<br />

Hyperthyroidism – thyroid acropachy JAAD 26:885–902, 1992<br />

Mucopolysaccharidoses – Sly syndrome, Hurler’s syndrome<br />

Multiple sulfatase deficiency – broad thumbs, ichthyosis,<br />

gargoylism Ped Derm 18:388–392, 2001<br />

Pulmonary osteoarthropathy<br />

Tuberous xanthomas JAAD 13:1–30, 1986<br />

NEOPLASTIC DISEASES<br />

Aggressive digital papillary adenoma (adenocarcinoma)<br />

Cutis 69:179–182, 2002; AD 120:1612, 1984<br />

Chondrosarcoma<br />

Connective tissue nevi JAAD 33:154–155, 1995<br />

Epidermal nevus JAAD 33:154–155, 1995<br />

Epidermoid cyst Rook p.2847, 1998, Sixth Edition; intraosseous<br />

epidermoid cyst BJD 145:366–368, 2001<br />

Epithelioid sarcoma JAAD 26:302–305, 1992<br />

Exostosis JAAD 19:132, 1988<br />

Fibrolipoma<br />

Fibromatosis – localized digital fibromatosis<br />

Acta DV 74:386–387, 1994; Clin Exp Dermatol<br />

16:121–123, 1991<br />

Fibro-osseous pseudotumor of the digits BJD 144:1274–1275,<br />

2001<br />

Fibrosarcoma<br />

Fibrous hamartoma Ped Derm 17:270–276, 2000<br />

Garlic clove tumor – acquired periungual fibrokeratoma<br />

Cutis 46:118–124, 1990<br />

Giant cell tumor of the tendon sheath BJD 146:125–128, 2002<br />

Glomus tumor<br />

Growth promoting neoplasm – adrenocortical tumor, testicular<br />

tumor, Wilms tumor Ped Derm 17:270–276, 2000<br />

Infantile desmoid-type fibromatosis Ped Derm 12:149–151, 1995<br />

Intraosseous chondroid syringoma JAAD 30:374–378, 1994<br />

Kaposi’s sarcoma – epidemic; endemic African Kaposi’s<br />

sarcoma JAAD 22:1237–1250, 1990<br />

Lipofibromatous hamartoma J Hand Surg 13:67–75,<br />

1988; lipofibromatous hamartoma of the median<br />

nerve Ped Derm 15:378–380, 1998; congenital<br />

lipofibromatosis Foot Ankle 12:40–46, 1991;<br />

hyperostotic macrodactyly and lipofibromatous hamartoma<br />

of the median nerve Chir Main 18:261–271, 1999;<br />

fibrolipomatous hamartoma of the nerve (nerve<br />

territory-oriented macrodactyly) (macrodystrophia lipomatosa)<br />

Skeletal Radiol 24:296–297, 1995

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