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Abstract:

This video presents a detailed comparison of two pathologically similar, rare, hypocellular fibrous tumors: Gardner fibroma and Nuchal-type fibroma. Using two case examples—one from a 5-year-old boy (Gardner fibroma) and one from a 30-year-old man (Nuchal-type fibroma)—the discussion highlights their shared histological features, which include circumscribed nodules of dense, sclerotic collagen with sparse bland spindle fibroblasts located in the subcutis. The primary and most critical factor for differentiation is established as patient age. A diagnosis of Gardner fibroma in a child necessitates workup to exclude associated Gardner Syndrome (Familial Adenomatous Polyposis), a critical concern not typically associated with the Nuchal-type variant found in adults. The role of nuclear beta-catenin immunohistochemistry in supporting the Gardner fibroma diagnosis and its potential link to desmoid fibromatosis is also noted.

Differential Diagnosis: Gardner Fibroma vs. Nuchal-Type Fibroma

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