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Fibrous dysplasia of bone. (Pathology Clinic).


Fibrous dysplasia (fibro-osseous metaplasia) is one of a diverse group of diseases that are characterized by alterations in bone growth. It is a developmental, tumor-like process of unknown etiology. Its initial clinical sign is usually a painless enlargement of the affected bone. It occurs in equal proportions in males and females, most often during the first two decades of life.

Fibrous dysplasia is subclassified into two main clinical subtypes: monostotic and polyostotic. The monostotic type, which accounts for 80% of cases, affects only one bone, usually the maxilla maxilla /max·il·la/ (mak-sil´ah) pl. maxil´las, maxil´lae   [L.] the irregularly shaped bone that with its fellow forms the upper jaw. max´illary

max·il·la
n. pl.
; the polyostotic type affects multiple bones. Polyostatic fibrous dysplasia is seen in both Jaffe-Lichtenstein and McCune-Albright syndromes, along with skin hyperpigmentation (cafe au lait tan macules) and sexual precocity (the most common endocrine disturbance). Radiologic studies typically demonstrate a poorly defined, ground-glass-type lesion; in the polyostotic form, multilocular multilocular /mul·ti·loc·u·lar/ (-lok´u-ler) having many cells or compartments.

mul·ti·loc·u·lar
adj.
Having or consisting of many small compartments or cavities.
 radiolucencies may be seen.

Histologically, fibrous dysplasia features irregularly shaped trabeculae of immature, woven bone in a background of variably cellular, loosely arranged fibrous stroma stroma /stro·ma/ (stro´mah) pl. stro´mata   [Gr.] the matrix or supporting tissue of an organ.stro´malstromat´ic

stro·ma
n. pl. stro·ma·ta
1.
 (figure 1). The spicules of bone are often curvilinear or branching, and they have a "Chinese character" or "alphabet soup" appearance. The delicate trabeculae do not have osteoid osteoid /os·te·oid/ (os´te-oid)
1. resembling bone.

2. the organic matrix of bone; young bone that has not undergone calcification.


os·te·oid
adj.
Resembling bone.
 rims, but they do have minimal osteoblastic osteoblastic

emanating from or pertaining to an osteoblast.
 rimming (figure 2). The fibroblasts usually have plump, ovoid o·void or o·voi·dal
n.
Something that is shaped like an egg.

adj.
Shaped like an egg; oviform.



ovoid

having the oval shape of an egg.


ovoid body
colloid body.
 nuclei, although elongated, narrow nuclei are sometimes also seen.

Treatment of fibrous dysplasia is challenging. Bone growth can stop spontaneously, but by then it might have already resulted in a cosmetic deformity that requires surgical excision. Regrowth occurs in as many as 50% of patients over time. Irradiation is not indicated.

Suggested reading

El-Mofty SK, Kyriakos M. Soft tissue and bone lesions. In: Gnepp DR, ed. Diagnostic Surgical Pathology of the Head and Neck. Philadelphia: W.B. Saunders, 2001:505-604.

Waldron CA. Bone pathology. In: Neville BW, Damm DD, Allen CM, Bouquot JE, eds. Oral and Maxillofacial Pathology. Philadelphia: W.B. Saunders, 1995:443-92.

Waldron CA. Fibro-osseous lesions of the jaws. J Oral Maxillofac Surg 1993;51:828-35.

From the Department of Endocrine and Otorhinolaryngic-Head and Neck Pathology, Armed Forces Institute of Pathology Armed Forces Institute of Pathology A section of the US military which provides consultations, reference atlases and educational programs for pathologists , Washington, D.C.
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Author:Thompson, Lester D.R.
Publication:Ear, Nose and Throat Journal
Geographic Code:1USA
Date:Apr 1, 2003
Words:341
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