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Pathology of the Head and Neck

Pathology of the Head and Neck

Pathology of the Head and Neck

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122 P.J. Slootweg4Fig. 4.29. Ossifying fibroma contains both cell-rich <strong>and</strong> cell-poorareas as well as well-structured bone <strong>and</strong> amorphous calcified materialFig. 4.31. Juvenile trabecular ossifying fibroma shows slenderbony trabeculae rimmed with osteoblasts that merge with an extremelycellular stromaFig. 4.30. Ossifying fibroma may also contain more smoothlycontoured bony elements, formerly thought to represent cementumFig. 4.32. At higher magnification, <strong>the</strong> plump osteoblasts thatline <strong>the</strong> bony trabeculae in juvenile trabecular ossifying fibromaare shown to be a prominent featureOssifying fibroma is composed <strong>of</strong> fibrous tissue thatmay vary in cellularity from areas with closely packedcells displaying mitotic figures to almost acellular sclerosingparts within one <strong>and</strong> <strong>the</strong> same lesion. The mineralisedcomponent may consist <strong>of</strong> plexiform bone, lamellar bone<strong>and</strong> acellular mineralised material, sometimes all occurringtoge<strong>the</strong>r in one single lesion (Figs 4.29, 4.30).Juvenile psammomatoid <strong>and</strong> juvenile trabecular ossifyingfibroma are subtypes [40]. Juvenile trabecularossifying fibroma consists <strong>of</strong> cell-rich fibrous tissuewith b<strong>and</strong>s <strong>of</strong> cellular osteoid toge<strong>the</strong>r with slendertrabeculae <strong>of</strong> plexiform bone lined by a dense rim<strong>of</strong> enlarged osteoblasts (Figs. 4.31, 4.32). Sometimes<strong>the</strong>se trabeculae may anastomose to form a lattice.Mitoses are present, especially in <strong>the</strong> cell-rich areas.Also, multinucleated giant cells, pseudocystic stromaldegeneration <strong>and</strong> haemorrhages may be present. Dueto its cellularity <strong>and</strong> mitotic activity, <strong>the</strong> lesion may beconfused with osteosarcoma. However, atypical cellularfeatures or abnormal mitotic figures are not seen.Moreover, <strong>the</strong> lesion is demarcated from its surroundings[73, 158, 181].Juvenile psammomatoid ossifying fibroma is characterisedby a fibroblastic stroma containing small ossiclesresembling psammoma bodies, hence its name. Thestroma varies from loose <strong>and</strong> fibroblastic to intenselycellular. The spherical or curved ossicles are acellularor include sparsely distributed cells (Fig. 4.33). Theyshould not be confused with <strong>the</strong> cementum-like depositsthat are present in conventional ossifying fibroma.These particles have a smooth contour whereas <strong>the</strong> ossiclesin juvenile psammomatoid ossifying fibroma hasa peripheral radiating fringe <strong>of</strong> collagen fibres. Ossiclesmay coalesce to form trabeculae. Sometimes, juvenilepsammomatoid ossifying fibroma contains basophilic,concentrically lamellated particles, as well as irregularthread-like or thorn-like calcified str<strong>and</strong>s in a hyalinisedbackground (Fig. 4.34). O<strong>the</strong>r features such as trabeculae<strong>of</strong> woven bone as well as lamellar bone, pseudocysticstromal degeneration <strong>and</strong> haemorrhages resulting

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