Download Differential Diagnosis for the Dermatologist by Scott M. Jackson, Lee T. Nesbitt (auth.) PDF

By Scott M. Jackson, Lee T. Nesbitt (auth.)

When confronted with a not easy dermatologic challenge, physicians are usually required to accomplish a time-consuming seek via huge dermatologic texts as a way to locate details that might help in the mandatory differential analysis. This complete and concise guide is designed to simplify this approach dramatically, allowing swift id of the proper analysis. thousands of dermatologic diagnoses, morphologic good points, drug-induced problems, extracutaneous manifestations, histologic findings, and random different findings are indexed in alphabetical order and in a homogeneous, reader-friendly constitution. The differential diagnoses are proven less than each one major prognosis, looked after in accordance with similarity with that analysis. because the first variation, impending 50 new diagnoses were additional, and plenty of new photographs integrated. This simply transportable publication should be of serious worth for dermatologists and all who take care of dermatologic diseases.

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Am J Gastroenterol 101(3):541–546 Cleft Lip and/or Palate • • • • • • • • • • • • • • • • • 4p syndrome Hay−Wells syndrome Beare−Stevenson cutis gyrata syndrome Branchio-oculo-facial syndrome Cleft lip/palate − ectodermal dysplasia syndrome Dermal melanocytosis EEC syndrome Encephalocele Nasal glioma Nail−patella syndrome Nevoid basal cell carcinoma syndrome Oculocerebrocutaneous syndrome Oral−facial−digital syndrome Popliteal pterygium syndrome Rapp−Hodgkin syndrome Robert syndrome Van der Woude syndrome Chapter 2 32 • • Waardenburg syndrome, type 1 or 3 Wolf−Hirschhorn syndrome Further reading: • Steele JA, Hansen H, Arn P, Kwong PC (2005) Spectrum of phenotypic manifestations from a single point mutation of the p63 gene, including new cutaneous and immunologic findings.

Pediatr Dermatol 19(6):550–552 Gastrointestinal Hemorrhage • • • • • • • • • • Blue rubber bleb nevus syndrome Chronic urticaria (H. pylori infection) Cowden’s disease Crohn’s disease Cronkhite–Canada syndrome Diffuse neonatal hemangiomatosis Ehlers–Danlos syndrome, type IV Gardner’s syndrome Hemangiomatosis Henoch–Schönlein purpura The Past Medical History, Social History, and Review of Systems • • • • • • • • • • • • Hereditary hemorrhagic telangiectasia Kaposi’s sarcoma Kawasaki disease Maffucci’s syndrome Malignant atrophic papulosis Muir–Torre syndrome Peutz–Jeghers syndrome Polyarteritis nodosa Pseudoxanthoma elasticum Scurvy Ulcerative colitis Vasculitis Further reading: • Braverman IM (2003) Skin signs of gastrointestinal disease.

1 Acral acanthosis nigricans Chapter 2 36 • • • • • • • • • • Injection lipoatrophy Mucormycosis Necrobiosis lipoidica Neuropathic ulcers Partial lipodystrophy Perforating disorders Pruritus Rubeosis Scleredema adultorum Xerosis Further reading: • Ahmed I, Goldstein B (2006) Diabetes mellitus. Clin Dermatol 24(4):237–246 Digital Anomalies • • • • • • • • • • • • • • • Adams–Oliver syndrome Apert syndrome Cleft lip/palate–ectodermal dysplasia EEC syndrome Epidermal nevus syndrome Focal dermal hypoplasia Klippel–Trenaunay syndrome Limb–mammary syndrome Nevoid basal cell carcinoma syndrome Oculodentodigital syndrome Oral–facial–digital syndrome Popliteal pterygium syndrome Proteus syndrome Trichorhinophalangeal syndrome Waardenburg syndrome, type 3 Further reading: • Kalla G, Garg A (2002) Ectrodactyly.

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