Soft tissue, neurofibroma

Details
Disease Category
Gender
Age
53 years
Organ System/Discipline
Diagnosis
Neurofribroma
Clinical History

The patient has a history of Neurofibromatosis Type 1. She developed a retroperitoneal malignant peripheral nerve sheath tumour, which was resected and treated with adjuvant radiation. This specimen represents incidental skin nodules found at the time of surgical evaluation.

Case Discussion

Neurofibroma is a tumour of the cells of the nerve sheath that can occur both associated with neurofibromatosis (especially NF1) or sporadically. This example is from a patient with known NF1. The findings are of a well demarcated non-encapsulated cutaneous tumour composed of interlacing fascicles of bland spindled-to-ovoid cells with wavy dark nuclei. There is no mitotic activity or necrosis. The underlying stroma consists of coarse collagen bundles and the overlying epidermis is unremarkable.

Image Contributors
Mrkonjic, M., Chang, M.

Cite

Mrkonjic, M., Chang, M. Soft tissue, neurofibroma. Digital Laboratory Medicine Library, Dept of Laboratory Medicine & Pathobiology, University of Toronto. Published . Accessed December 17, 2025. https://dev.dlml.cflabs.ca/image/soft-tissue-neurofibroma-lmp16706