Schneiderman Prelims Vol-I. qxd

MACRODACTYLY (ENLARGED DIGIT)
327
Schneiderman page 300-400.qxd 5/16/2006 6:50 PM Page 327

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Gout
Median nerve injury
Osteoid osteoma 
Rook p.2847, 1998, Sixth Edition
Sarcoid
Trauma
Unilateral
Aneurysm – left innominate artery
Axillary Pancoast tumors
Brachial arteriovenous aneurysm
Patent ductus arteriosus with pulmonary hypertension
Prolonged hemiplegia
Bronchogenic carcinoma
Bronchiectasis, cysts
Carcinoma of the nasopharynx, colon, esophagus, stomach
Ghatan p.79, 2002, Second Edition
Celiac sprue 
JAAD 52:1020–1028, 2005
CINCA syndrome 
JAAD 52:1020–1028, 2005
Cirrhosis
Crohn’s disease
Congestive heart failure
Cyanotic congenital heart disease
JAAD 52:1020–1028, 2005
Cystic fibrosis 
JAAD 52:1020–1028, 2005
Diarrhea, chronic
Down’s syndrome
Familial
Hemochromatosis
Hereditary – autosomal dominant
Hereditary mucoepithelial dysplasia
HIV disease 
JAAD 52:1020–1028, 2005
Hyperparathyroidism
Hypertrophic osteoarthropathy
Hypersensitivity pneumonitis 
JAAD 52:1020–1028, 2005
Hypervitaminosis A
Idiopathic
Idiopathic pulmonary fibrosis 
JAAD 52:1020–1028, 2005
Infective endocarditis 
JAAD 52:1020–1028, 2005
Inflammatory bowel disease 
JAAD 52:1020–1028, 2005
Juvenile polyposis coli 
JAAD 52:1020–1028, 2005
Laxative abuse 
SMJ 76:1071, 1983; Lancet 2:947, 1978
Liver disease 
JAAD 52:1020–1028, 2005
Lung abscess, empyema
Lupus erythematosus 
BJD 89:533–535, 1973
Lymphoma 
JAAD 52:1020–1028, 2005
Malabsorption
Malaria
Malnutrition 
Ghatan p.79, 2002, Second Edition
Marfan’s syndrome – pseudoclubbing
Myxedema, Graves’ disease (thyroid acropachy) 
Med Clin
North Am 52:393–395, 1968
Marie–Bamberger syndrome
Mesothelioma 
JAAD 52:1020–1028, 2005
Nasopharyngeal carcinoma 
JAAD 52:1020–1028, 2005
Parasitic bacillary dysentery 
JAAD 52:1020–1028, 2005
Phosphorus toxicity
Pleural tumors 
JAAD 52:1020–1028, 2005
POEMS syndrome 
JAAD 52:1020–1028, 2005
Polycythemia
Psoriatic onycho-pachydermoperiostitis 
BJD 143:901–902,
2000; Rev Rheum Mal Osteoartic 56:579–582, 1989
Pulmonary arteriovenous malformation 
JAAD
52:1020–1028, 2005
Pycnodysostosis – pseudoclubbing (acro-osteolysis) 
Br Med
J iii:712–714, 1967
Sarcoidosis 
JAAD 52:1020–1028, 2005
Sprue
Subacute bacterial endocarditis
Syringomyelia
Systemic lupus erythematosus
Thymoma, malignant
Thyroid disease 
JAAD 52:1020–1028, 2005
Tuberculosis 
JAAD 52:1020–1028, 2005
Ulcerative colitis
Venous stasis 
JAAD 52:1020–1028, 2005
X-linked reticulate pigmentary disorder with
systemic manifestations (familial cutaneous amyloidosis)
(Partington syndrome II) – X-linked; rare; Xp21–22; boys
with generalized reticulated muddy brown pigmentation
(dyschromatosis) with hypopigmented corneal
dystrophy (dyskeratosis), coarse unruly hair,
unswept eyebrows, silvery hair, hypohidrosis, recurrent
pneumonia with chronic obstructive disease, clubbing;
failure to thrive, female carriers with linear macular nevoid
Blascko-esque hyperpigmentation 
Ped Derm 22:122–126,
2005; Semin Cut Med Surg 16:72–80, 1997;
Am J Med Gen 10:65:1981
Gout
Hyperthyroidism – thyroid acropachy 
JAAD 26:885–902, 1992
Mucopolysaccharidoses – Sly syndrome, Hurler’s syndrome
Multiple sulfatase deficiency – broad thumbs, ichthyosis,
gargoylism 
Ped Derm 18:388–392, 2001
Pulmonary osteoarthropathy
Tuberous xanthomas 
JAAD 13:1–30, 1986