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Quick Review for Patients
Note: click on underlined words for more detail or photos. The giant cell fibroma is a subtype of irritation fibroma, i.e.
it is a localized inflammatory fibrous hyperplasia, but it differs significantly
from routine fibromas in that its stroma contains scattered fibroblasts with
very large, usually angular (stellate), but not hyperchromatic nuclei.
Lesions with similar histology are found at other body sites, especially the
skin of the nose (fibrous papule of the nose), the uterine cervix, vagina,
bladder and other skin areas.
Clinical Features This
type of fibroma can be seen at any age and on any oral mucosal surface, but it
has a predilection for gingival, lateral tongue and tip of tongue
locations. It seldom becomes more than 0.5 cm. in greatest diameter and
often are comprised of two or three lobules, or may have a few small papules on
the surface. Most lesions are pedunculated but sessile examples are not
unusual. The surface is almost never ulcerated, unless acutely
traumatized, and the color is that of the surrounding normal mucosa (Figures
1 & 2). Occasional patients will have multiple lesions but they
are seldom numerous. Pathology and Differential Diagnosis The lesion is characterized by a diffuse, somewhat immature,
rather avascular collagenic stroma with small bipolar and slightly stellate
fibroblasts scattered throughout in moderate numbers. Occasional
fibroblasts will be quite large and angular, and may have more than one nucleus (Figure
3). These pathognomonic cells are never hyperchromatic, as they would
be if they were truly dysplastic fibroblasts, and they often have a smudged
appearance. They are most numerous in the zone immediately beneath the
covering epithelium. The epithelium is usually normal but may have
elongated and narrow rete ridges. At the inferior margin the lesional
fibrosis blends into the normal underlying fibrovascular tissues, with no
capsule or pseudocapsule. Occasional lymphocytes may be seen beneath the
epithelium or around capillaries. Treatment and Prognosis
The giant cell fibroma is treated by conservative surgical removal but is more
likely to recur with this treatment than a more routine irritation fibroma, even
when that fibroma is much larger. If left alone, the giant cell fibroma
will not enlarge indefinitely, but will reach its maximum size within a few
months and remain unchanged thereafter, unless acute trauma produces edema or
areas of granulation tissue proliferation.
References (Chronologic Order) Note: General references can be found by clicking on that topic to the left. Weathers DR, Callihan MD. Giant-cell fibroma. Oral Surg Oral Med Oral Pathol 1974; 37:374-384. Houston GD. The giant cell fibroma. A review of 464 cases. Oral Surg Oral Med Oral Pathol 1982; 53:582-587. Reibel J. Oral fibrous hyperplasias containing stellate and multinucleated cells. Scand J Dent Res 1982; 90:217-226. Regezi JA, Courtney RM, Kerr DA. Fibrous lesions of the skin and mucous membranes which contain stellate and multinucleated cells. Oral Surg Oral Med Oral Pathol 1985; 39:605-614. Pitrt MA, Roberts ISD, Agambu DA, et al. The nature of atypical multinucleated stromal cells: a study of 37 cases from different sites. Histopathol 1993; 23:137-145. Odell EW, Lock C, Lombardi TL. Phenotypic characterization of stellate and giant cells in giant cell fibroma by immunocytochemistry. J Oral Pathol Med 1994; 23:284-287. Note: To see enlarged photo, click on
the left-hand picture;
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Figure 1: Giant cell fibroma of the lateral tongue is characteristically small and painless, and has small surface nodules or papules. Photo courtesy of Dr. John Alonge, Erie, PA. [return to text] |
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Figure 2: A sessile giant cell fibroma of the buccal mucosa was found in the same patient as Figure 1. Multiple lesions are unusual. Photo courtesy of Dr. John Alonge, Erie, PA [return to text] |
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Figure 3: Scattered fibroblasts located just beneath the epithelium are enlarged and angular but are not hyperchromatic. Some cells have multiple nuclei. [return to text] |
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