Schwannoma of the Upper Extremity: Retrospective Analysis of 17 Cases

Authors

  • Ângelo Sá Serviço de Cirurgia Plástica, Reconstrutiva e Maxilo-Facial. Hospital Egas Moniz. Centro Hospitalar de Lisboa Ocidental. Lisboa. Portugal.
  • Leandro Nobre Azevedo Serviço de Cirurgia Plástica, Reconstrutiva e Maxilo-Facial. Hospital Egas Moniz. Centro Hospitalar de Lisboa Ocidental. Lisboa. Portugal.
  • Luísa Cunha Serviço de Cirurgia Plástica, Reconstrutiva e Maxilo-Facial. Hospital Egas Moniz. Centro Hospitalar de Lisboa Ocidental. Lisboa. Portugal.

DOI:

https://doi.org/10.20344/amp.6906

Keywords:

Hand, Neurilemmoma, Soft Tissue Neoplasms, Upper Extremity.

Abstract

Introduction: Schwannoma or neurilemmoma is a benign peripheric nerve tumor that usually presents as a slow growing single lesion; it has origin in Schwann cells proliferation. Although it represents a small percentage of the benign tumors of the upper arm, it is the most frequent of neural origin. We present a retrospective study of upper limb schwannomas; our aim is establish the appropriate preoperative approach, to recognise the efficiency of the treatment and the pos-operative follow-up.
Material and Methods: Review of 17 patients treated between 2007 and 2014 with upper limb schwannoma and characterization as to age, gender, location in the upper limb, signs and symptoms, pre-operative studies, histologic diagnosis and postoperative surveillance.
Results: In four of them the schwannoma was localized on the arm, three on the forearm, four on the wrist and 6 on the hand or fingers. We proceed to careful microsurgical dissection in a bloodless field to optimize the functional final result. The enucleation without fascicular lesion was achieved in 12 patients. In five patients we performed the excision of the fascicles involved by the mass. Nine patients developed paresthesias in the immediate postoperative period, with five of them improving in 12 months. One patient presented motor deficit of the radial nerve with partial recover at 12 monts.
Discussion: Schwannomas are rare tumours with well circumscribed morphology. Occasionally it appears in upper limb. The preoperative
diagnosis is rarely, so normally the diagnosis is established only after excision and histologic study.
Conclusion: Schwannoma should be considered as a diagnostic hypothesis when evaluating subcutaneous nodes associated with
neurologic symptoms. It is important to query the presence of paresthesias and perform the Tinel sign, both typical of this condition.
Imagiological exams have a scarce contribute in the diagnosis. To improve the final result, the preoperative study must be insightful, being advisable to consider the benefits of the surgery compared to the potential iatrogenic damage to the nerve.

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Published

2016-09-30

How to Cite

1.
Sá Ângelo, Azevedo LN, Cunha L. Schwannoma of the Upper Extremity: Retrospective Analysis of 17 Cases. Acta Med Port [Internet]. 2016 Sep. 30 [cited 2024 Nov. 22];29(9):519-24. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/6906

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Section

Original