Malignant Peripheral Nerve Sheath Tumors of the Brachial Plexus - A Case Report
PDF

Keywords

Neurosarcoma
Radiotherapy
Surgery

How to Cite

1.
Rhaouti M, Lamouime F, Lakranbi M, Smahi M. Malignant Peripheral Nerve Sheath Tumors of the Brachial Plexus - A Case Report. ATD [Internet]. 2023 Apr. 2 [cited 2024 Nov. 21];2023. Available from: https://mbmjpress.com/index.php/atd/article/view/687

Abstract

Introduction: Malignant peripheral nerve sheath tumors represent all the neoplasias developed at the expense of cells located in the peripheral nerve sheaths. Complete surgical excision with microscopically healthy edges remains the only curative treatment. Through a clinical case, and a review of the literature, we will report our experience in the management of a tumor of the peripheral nerve sheaths. Observation: Madam K.L, 34 years old, admitted for management of a spontaneously painful left axillary mass, and in whom the clinical examination found a patient, in good general condition, with the presence of a 8cm left axillary mass hard to fixed palpation in relation to the 2 planes, painless on palpation. Thoracic computed tomography revealed an encapsulated left axillary tissue mass compressing the axillary pedicle measuring 84mm*67mm with areas of necrosis. MRI had objectified the presence of a fusiform mass extended to the inter-scalene space most likely evoking a tumor of the malignant peripheral nerve sheaths. The patient had undergone complete tumor excision with section of the left subclavian artery and end-to-end anastomosis, with simple postoperative consequences. Conclusion: MPNSTs are rare tumors. Surgery occupies an essential place in the treatment of this disease, it must be planned in order to avoid vascular and nervous risks. Radiotherapy may be indicated as an adjuvant or in the event of an unhealthy margin.

https://doi.org/10.15342/atd.2023.687
PDF

References

Ng, V.Y., et al., Incidence and survival in sarcoma in the United States: a focus on musculoskeletal lesions. Anticancer Res, 2013. 33(6): p. 2597-604.

ESMO / European Sarcoma Network Working Group, Soft tissue and visceral sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol, 2012. 23 Suppl 7: p.92-9.

Woodruff, J.M., Pathology of tumors of the peripheral nerve sheath in type 1 neurofibromatosis. Am J Med Genet, 1999. 89(1): p. 23-30.

Ducatman, B.S., et al., Malignant peripheral nerve sheath tumors. A clinicopathologic study of 120 cases. Cancer, 1986. 57(10): p. 2006-2021.

Anghileri, M., et al., Malignant peripheral nerve sheath tumors: prognostic factors and survival in a series of patients treated at a single institution. Cancer, 2006. 107(5): p. 1065-74.

Lafemina, J., et al., Oncologic Outcomes of Sporadic, Neurofibromatosis-Associated, and Radiation-Induced Malignant Peripheral Nerve Sheath Tumors. Ann Surg Oncol, 2012.

Porter, D.E., et al., Survival in Malignant Peripheral Nerve Sheath Tumours: A Comparison between Sporadic and Neurofibromatosis Type 1-Associated Tumours. Sarcoma, 2009. 2009: p. 756395.

Longhi, A., et al., High grade malignant peripheral nerve sheath tumors: outcome of 62 patients with localized disease and review of the literature. J Chemother, 2010. 22(6): p. 413-8.

Gronchi A, Olmi P, Casali PG. Expert Rev Anticancer Ther 2007; 7: 1135-44.

Stotter AT, A’Hern RP, Fisher C. The influence of local recurrence of extremity soft tissue sarcoma on metastasis and survival. Cancer 1990; 65: 1119-29.

Wanebo JE, Malik JM, Vandenberg SR, Wanebo HJ, Driesen N, Presing JA. Malignant peripheral nerve sheath tumors: a clinicopathologic study of 28cases cancer 1993; 71: 1247-53.

Adjuvant chemotherapy for localisedresectable soft-tissue sarcoma of adults: metaanalysis of individual data. Sarcoma Meta-analysis Collaboration. Lancet, 1997. 350(9092): p. 1647-54.

Wong, W.W., et al., Malignant peripheral nerve sheath tumor: analysis of treatment outcome. Int J Radiat Oncol Biol Phys, 1998. 42(2): p. 351-60.

Stucky, C.C., et al., Malignant peripheral nerve sheath tumors (MPNST): the Mayo Clinic experience. Ann Surg Oncol, 2012. 19(3): p. 878-85.

Sordillo, P.P., et al., Malignant schwannoma--clinical characteristics, survival, and response to therapy. Cancer, 1981. 47(10): p. 2503-9.

Dunn, G.P., et al., Role of resection of malignant peripheral nerve sheath tumors in patients with neurofibromatosis type 1. J Neurosurg, 2013. 118(1): p. 142-8.

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Copyright (c) 2023 Maroua Rhaouti

Metrics

Metrics Loading ...