Skip to main content
Log in

Fibromatosis Arising in Association with Neuromuscular Hamartoma of the Mandible

  • Case Report
  • Published:
Head and Neck Pathology Aims and scope Submit manuscript

Abstract

Aggressive fibromatosis is a benign but locally-aggressive tumor, which most often affects the muscles of the shoulder, the pelvic girdle, and the thigh. It usually affects adolescents and young adults. Desmoplastic fibroma, considered the bone counterpart of soft tissue fibromatosis, is a rare tumor that usually affects the metaphyseal or diaphyseal portions of long bones or, less commonly, the jaw. Neuromuscular hamartoma, a rare developmental lesion composed of mature elements of both striated muscle and nerve, is usually diagnosed in infants and children and affects large nerve trunks. Rarely, it can affect the head and neck region. Occasional cases showing an association between aggressive fibromatosis and neuromuscular hamartoma have been reported in the literature. Here we present a unique case of an adult patient with desmoplastic fibroma of the mandible in association with neuromuscular hamartoma.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10

References

  1. Griffith JG, Irby WB Desmoplastic fibroma. Report of a rare tumor of the oral structures. Oral Surg Oral Med Oral Pathol. 1965.

  2. Boman F, Palau C, Floquet A, Floquet J, Lascombes P. Neuromuscular hamartoma. Ann Pathol. 1991;11:36–41.

    PubMed  CAS  Google Scholar 

  3. Awasthi D, Kline DG, Beckman EN. Neuromuscular hamartoma (benign “triton” tumor) of the brachial plexus. Case report. J Neurosurg. 1991;75:795–7.

    Article  PubMed  CAS  Google Scholar 

  4. Castro DE, Raghuram K, Phillips CD. Benign triton tumor of the trigeminal nerve. Case report. AJNR Am J Neuroradiol. 2005;26:967–9.

    PubMed  Google Scholar 

  5. Vajramani G, Devi I, Santosh V, Hegde T, Das BS, Das S, et al. Benign triton tumor of the trigeminal nerve. Childs Nerv Syst. 1999;15:140–4.

    Article  PubMed  CAS  Google Scholar 

  6. Kim DH, Hong EK, Lee JD. Subcutaneous neuromuscular hamartoma. A case report. Korean J Pathol. 1999;33:62–4.

    Google Scholar 

  7. Bonneau R, Brochu P. Neuromuscular choristoma. A clinicopathologic study of two cases. Am J Surg Pathol. 1983;7:521–8.

    Article  PubMed  CAS  Google Scholar 

  8. Mitchell A, Scheithauer BW, Ostertag H, Sepehrnia A, Sav A. Neuromuscular choristoma. Am J Clin Pathol. 1995;103:460–5.

    PubMed  CAS  Google Scholar 

  9. Blouin MNH, Scheithauer BW, Amrami KK, Durham SR, Spinner RJ. Fibromatosis: a potential sequela of neuromuscular choristoma. J Neurosurg. 2012;116:399–408.

    Article  Google Scholar 

  10. Tiffee JC, Barnes EL. Neuromuscular hamartomas of the head and neck. Arch Otolaryngol Head Neck Surg. 1998;124:212–6.

    Article  PubMed  CAS  Google Scholar 

  11. Chen KT. Neuromuscular hamartoma. J Surg Oncol. 1984;26:158–60.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Leena Yaseen Taher.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Taher, L.Y., Saleem, M., Velagapudi, S. et al. Fibromatosis Arising in Association with Neuromuscular Hamartoma of the Mandible. Head and Neck Pathol 7, 280–284 (2013). https://doi.org/10.1007/s12105-012-0418-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12105-012-0418-8

Keywords

Navigation