Schneiderman Prelims Vol-I. qxd

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A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
Schneiderman page 600-722.qxd 5/16/2006 6:51 PM Page 666

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Sixth Edition; Int J Dermatol 27:49–53, 1988; BJD 116:31–37,
1987; Trans R Soc Trop Med Hyg 82:185–189, 1988
Tularemia 
Clin Inf Dis 20:174–175, 1995; Cutis 54:279–286,
1994
Yaws
INFLAMMATORY DISORDERS
Pyoderma gangrenosum 
Dermatology 195:50–51, 1997;
J Derm Surg Oncol 20:833–836, 1994; JAAD 18:559–568,
1988; pyoderma gangrenosum with C 7 deficiency JAAD
27:356–359, 1992; AD 22:655–680, 1930
METABOLIC DISEASES
Antithrombin III deficiency
Calciphylaxis
Metastatic Crohn’s disease – granulomatous ulcer
JAAD
41:476–479, 1999
Cryofibrinogenemia
Cryoglobulinemia
Essential thrombocythemia 
JAAD 24:59–63, 1991
Factor XII deficiency – livedo with ulceration 
BJD 143:897–899,
2000
Gaucher’s disease
Hemoglobinopathy (sickle cell anemia)
Homocysteinuria 
JAAD 40:279–281, 1999; Ned Tijdschr
Geneeskd 142:2706–2707, 1998 (Dutch)
Porphyrin retention
Prolidase deficiency – autosomal recessive; skin spongy and
fragile with annular pitting and scarring; leg ulcers;
photosensitivity, telangiectasia, purpura, premature graying,
lymphedema 
BJD 147:1227–1236, 2002; Ped Derm 13:58–60,
1996; AD 127:124–125, 1991; AD 123:493–497, 1987
Protein C deficiency – including IV catheter-induced thrombosis
in protein S deficiency 
JAAD 23:975–989, 1990
Protein S deficiency
Red blood cell disorders – sickle cell disease, hereditary
spherocytosis, thalassemia, polycythemia vera,
hereditary elliptocytosis, hereditary nonspherocytic hemolytic
anemia
Sickle cell ulcer 
Hematol Oncol Clin North Am 10:1333–1344,
1996