Clinical Guide to Oral Diseases. Crispian Scully

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I am especially indebted to my wife Vasiliki and my children Panagiotis and Katerina for their continuous love and support for all those years of my involvement in Oral Medicine, and during the preparation of this guide.

      Don't forget to visit the companion website for this book:

      www.wiley.com/go/malamos/clinical_guide

      There you will find valuable material designed to enhance your learning, including:

       Clinical cases

       Further reading

      Scan this QR code to visit the companion website

Section I

Common and important conditions
Local conditionsGingivitis/periodontitisGranuloma pyogenic/giant cellJaw fractureTraumaTumors invading blood vesselsSystemic conditionsCongenitalHemophilia A or BVon Willebrand's diseaseOther factor deficienciesGlanzman thrombastheniaAcquiredrelated to coagulationLiver diseaseVit. K deficiency, warfarin drug useDisseminated intravascular coagulationrelated to thrombocytopeniaIdiopathicDrug‐inducedCollagen vascular diseaseSarcoidosisHemolytic anemiaLeukemiaMyelomaWaldestmomrelated to platelet dysregulationAlcoholismChronic renal failureDrugsLiver diseaserelated to vascular disordersAngina bullosa hemorrhagicaAngiomasEhrler‐Danlos syndromeHereditary hemorrhagic telangiectasiaInfections from Ebola, HIV, HSV; EBV, RubellaMarfan syndromePurpuraScurvyrelated to fibrinolysisAmyloidosisStreptokinase treatment

      Case 1.1

      CO: A 62‐year‐old woman was referred by her family doctor for evaluation of several red spots on her lips, mouth, and the skin of her fingers.

      HPC: The red spots had been present since childhood, but had become greater on the surface of her face over the last five years causing cosmetic problems and patient’s concern.

      Q1 Which is the possible cause of her red spots?

      1 Crest syndrome

      2 Sjogren syndrome

      3 Rendu‐Osler‐Weber syndrome

      4 Rosacea

      Ataxiatelangiectasia

      Answers:

      1 No

      2 No

      3 Rendu‐Osler‐Weber syndrome or hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant condition that affects blood vessels throughout the body (telangiectasia; arteriovenous malformations) with a tendency for bleeding. This vascular dysplasia is commonly seen in oral, nasopharynx, lung, liver, spleen, gastrointestinal and urinary tracts, conjunctiva and the skin of arms and fingers.

      4 No

      5 No

      Comments: Skin telangiectasias are also seen in patients with ataxia telangiectasia, Crest and Sjogren syndromes. In rosacea, main vascular lesions are the broken vessels that are located exclusively on the skin predominantly on the middle of the face, as in ataxia telangiectasia. In ataxia telangectasia, the vascular lesions are associated with poor coordination, and in Crest syndrome with calcinosis and sclerodactyly and Raynaud phenomenon. Sjogren's syndrome affects the mouth, eyes, nose and other organs causing dryness, swelling of the salivary glands and facial telangiectases.

      Q2 Which are the main complications of this condition?

      1 Anemia

      2 Pulmonary hemorrhage

      3 Ischemic stroke

      4 Skin photosensitivity

      5 Mental retardation

      Answers:

      1 Iron

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