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    Paget's Disease

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    Pooja Patil
    This document provides information on Paget's disease, including its etiology, clinical features, oral manifestations, histological features, radiographic features, treatment, and prognosis. Paget's disease is characterized by excessive and abnormal bone remodeling, leading to enlarged and deformed bones. The cause is unknown but may be genetic or due to viral infection. Clinically, it most commonly affects bones after age 50 and presents as bone pain, warmth, and headaches. Oral manifestations include jaw enlargement and tooth migration. Histologically, there is disorganized bone formation by abnormal osteoclasts and osteoblasts. Radiographically, bones have a cotton wool appearance. Treatment focuses on suppressing bone resorption using calcitonin or

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    Paget's Disease

    Uploaded by

    Pooja Patil
    427 views13 pages
    This document provides information on Paget's disease, including its etiology, clinical features, oral manifestations, histological features, radiographic features, treatment, and prognosis. Paget's disease is characterized by excessive and abnormal bone remodeling, leading to enlarged and deformed bones. The cause is unknown but may be genetic or due to viral infection. Clinically, it most commonly affects bones after age 50 and presents as bone pain, warmth, and headaches. Oral manifestations include jaw enlargement and tooth migration. Histologically, there is disorganized bone formation by abnormal osteoclasts and osteoblasts. Radiographically, bones have a cotton wool appearance. Treatment focuses on suppressing bone resorption using calcitonin or

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    PAGET’S DISEASE

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    This document provides information on Paget's disease, including its etiology, clinical features, oral manifestations, histological features, radiographic features, treatment, and prognosis. Paget's disease is characterized by excessive and abnormal bone remodeling, leading to enlarged and deformed bones. The cause is unknown but may be genetic or due to viral infection. Clinically, it most commonly affects bones after age 50 and presents as bone pain, warmth, and headaches. Oral manifestations include jaw enlargement and tooth migration. Histologically, there is disorganized bone formation by abnormal osteoclasts and osteoblasts. Radiographically, bones have a cotton wool appearance. Treatment focuses on suppressing bone resorption using calcitonin or

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PPTX, PDF, TXT or read online from Scribd
    Download as pptx, pdf, or txt
    427 views13 pages

    Paget's Disease

    Uploaded by

    Pooja Patil
    This document provides information on Paget's disease, including its etiology, clinical features, oral manifestations, histological features, radiographic features, treatment, and prognosis. Paget's disease is characterized by excessive and abnormal bone remodeling, leading to enlarged and deformed bones. The cause is unknown but may be genetic or due to viral infection. Clinically, it most commonly affects bones after age 50 and presents as bone pain, warmth, and headaches. Oral manifestations include jaw enlargement and tooth migration. Histologically, there is disorganized bone formation by abnormal osteoclasts and osteoblasts. Radiographically, bones have a cotton wool appearance. Treatment focuses on suppressing bone resorption using calcitonin or

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PPTX, PDF, TXT or read online from Scribd
    Download as pptx, pdf, or txt
    of 13

    PAGETS DISEASE

    INTRODUCTION
    Pagets disease is named after Sir James Paget , an English surgeon who described the clinical course of this disorder under the name of osteitis deformans Pagets disease is characterized by excessive and abnormal remodeling of bone The excessive remodeling gives rise to bones that are extensively vascularized, weak, enlarged and deformed with subsequent complications Common in middle aged and elderly patients

    ETIOLOGY
    Etiology of Paget's disease is still unknown But possible etiology include Genetic Viral infection Inflammatory cause Autoimmune disorders Connective tissue and vascular disorders

    CLINICAL FEATURES
    Prevalence of Paget's disease increases with age Most commonly diagnosed after 50 years and rarely in people younger than 20 years Systemic findings include: almost all bones can be involved The major characteristic is enlargement of affected bone Patient complains of bone pain perceived as a dull constant aching pain deep below the soft tissues The involved bones becomes warm to touch because of the increased vascularity Non specific headaches, impaired hearing and tinnitus are common symptoms of Paget's disease

    ORAL MANIFESTATIONS include Involvement of jaws Maxilla exhibits progressive enlargement, the alveolar ridge becomes widened and palate is flattened If teeth are present, they become loose and migrate, producing some spacing When mandible is involved, findings are similar but not usually as severe as in maxilla As disease progress, mouth may remain open, exposing teeth, because the lips are too small to cover the enlarged jaw Edentulous patients complain of inability to wear dentures because of increasing tightness due to expansion of jaw

    Increase in the size of maxillary alveolar bone and drifting of teeth Pagets disease in 67 yr old woman showing enlargement of maxilla and protrusion of upper lip. Also there is deformity present at the root of the nose

    Enlargement on the right maxilla. Patient was unable to use denture

    HISTOLOGICAL FEATURES
    Paget's disease is characterized by enhanced resorption of bone by giant multinucleated osteoclast with formation of disorganized woven bone by osteoblast this process evolves through various phases of activity, followed by a quiescent stage Hence, Paget's disease consist of following 3 phases: Lytic Mixed lytic and blastic Sclerotic or burned out

    Initial osteolytic phase is marked by disordered areas of resorption by an increased number of overtly large osteoclasts (these abnormal osteoclast consist of as many as 100 nuclei)

    The next osteoblastic phase follows with haphazard laying of new bone matrix and formation of woven bone Repeated episodes of bone removal and formation results in appearance of many small irregularly shaped bone fragments that appear to be joined in jigsaw or mosaic pattern with deeply staining hematoxyphilic reversal lines. This pattern is histologic hallmark of Paget's disease Osteoblastic phase includes excessive abnormal bone formation causing more compact and dense bone The Paget's bone is coarse with an affinity for calcium and phosphorus Marrow spaces are filled with loose highly vascularized connective tissue- this causes increase in the regional blood flow and thus leads to rise in skin temperature seen clinically Pagetic bone shows no tendency to form haversian systems or to centre on blood vessels; the bones are very hard and dense Eventually osteoblastic activity diminishes and osteoporotic or burned out phase predominates The new bone is disordered, poorly mineralized and lacks structural integrity The proliferation of bone and concomitant hypercementosis sometimes results in obliteration of PDL

    Histology of Paget's disease shows several bone spicules in highly vascularized connective tissue stroma

    Higher magnification : A- osteoclast in howship lacunae B- osteoblast in process of bone formation

    MOSAIC PATTERN IN PAGETS DISEASE

    RADIOGRAPHIC FEATURES

    In Paget's disease, there is initial phase of deossification and softening, followed by bizarre, dysplastic type of reossification Osteoblastic areas are opaque radiographically and patchy in distribution Poorly defined areas of osteoporosis are noted Loss of normal trabeculation and appearance of irregular osteoblastic activity gives rise to typical cotton wool appearance of Paget's bone Teeth and adjacent bone also show radiographic changes : pronounced hypercementosis and loss of well defined lamina dura Root resorption is reported in some cases but it is unusual

    Radiographic image shows typical cotton wool appearance in Paget's disease

    Hypercementosis and loss of lamina dura

    TREATMENT AND PROGNOSIS


    There is no specific treatment for Paget's disease Very promising results have been recently obtained in treatment of this disease by use of CALCITONIN, the parathormone antagonist produced by thyroid gland which suppresses bone resorption BIPHOSPHANATES are also used since they inhibit bone resorption and as well as bone mineralization One of the cytotoxic antibiotics, MITHRAMYCIN has been used therapeutically but has serious side effects

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