Schneiderman Prelims Vol-I. qxd

INFILTRATIVE DISEASES
Amyloidosis 
JAAD 52:1009–1019, 2005
Intravascular or intralymphatic histiocytosis in rheumatoid
arthritis – livedoid red patches 
JAAD 50:585–590, 2004
INFLAMMATORY DISEASES
Fibromyalgia 
JAAD 52:1009–1019, 2005
Pancreatitis, chronic – livedo reticularis; ‘Walzel’s sign’
JAAD 39:1035–1036, 1998
METABOLIC
Anti-thrombin III deficiency 
JAAD 52:1009–1019, 2005
Calciphylaxis (vascular calcification cutaneous necrosis
syndrome) (chronic renal failure and hyperparathyroidism)
JAAD 40:979–987, 1999; JAAD 33:53–58, 1995; JAAD
33:954–962, 1995;J Dermatol 28:27–31, 2001; Br J Plast
Surg 53:253–255, 2000; J Cutan Med Surg 2:245–248, 1998;
JAAD 33:954–962, 1995; AD 131:786, 1995; AD 127:225–230,
1991; Arch Int Med 136:1273–1280, 1976; acute reversible
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renal failure; associated with hepatitis C infection
JAAD 50:S125–128, 2004
Cardiac failure 
JAAD 52:1009–1019, 2005
Cold agglutininemia 
Rook p.964, 1998, Sixth Edition
Cretinism – coarse facial features, lethargy, macroglossia,
cold dry skin, livedo, umbilical hernia, poor muscle tone, coarse
scalp hair, synophrys, no pubic or axillary hair at puberty
Rook p.2708, 1998, Sixth Edition
Cryofibrinogenemia 
Am J Med 116:332–337, 2004
Cryoglobulinemia 
JAAD 48:311–340, 2003; Rook p.964, 1998,
Sixth Edition
Cushing’s syndrome 
JAAD 52:1009–1019, 2005
Diabetes mellitus – peripheral neuropathy 
JAAD 52:1009–1019,
2005
Disseminated intravascular coagulation, including symmetric
peripheral gangrene 
JAAD 52:1009–1019, 2005
Hemolytic uremic syndrome 
JAAD 52:1009–1019, 2005
Homocystinuria – cystathionine-beta synthase deficiency
JAAD 40:279–281, 1999
Hypercalcemia 
JAAD 52:1009–1019, 2005
Hyperparathyroidism with vascular calcification 
Rook p.964,
1998, Sixth Edition
Hyperviscosity
Hypothyroidism 
JAAD 52:1009–1019, 2005
Pellagra 
JAAD 52:1009–1019, 2005
Pernicious anemia 
JAAD 52:1009–1019, 2005
Pregnancy – cutis marmorata of legs 
Ghatan p.297, 2002,
Second Edition
Primary oxalosis (primary hyperoxaluria) – type 1 – alanine
glyoxalate aminotransferase (transaminase) deficiency;
chromosome 2q36–37; type 2 (rare) – 
D
-glyceric acid
dehydrogenase deficiency 
JAAD 49:725–728, 2003; JAAD
46:S16–18, 2002; AD 137:957–962, 2001; JAAD 22:952–956,
1990; AD 131:821–823, 1995; AD 125:380–383, 1989; livedo
reticularis, ulcers, and peripheral gangrene 
AD 136:1272–1274,
2000
Protein S and C deficiency 
JAAD 52:1009–1019, 2005
Renal disease, chronic – calciphylaxis
Thrombocytopathy 
JAAD 52:1009–1019, 2005
Thrombotic thrombocytopenic purpura 
JAAD 52:1009–1019, 2005