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Plexiform Schwannoma of the Tongue in a Pediatric Patient with Neurofibromatosis Type 2: A Case Report and Review of Literature.
Amer, Samir M; Ukudeyeva, Aijan; Pine, Harold S; Campbell, Gerald A; Clement, Cecilia G.
Afiliação
  • Amer SM; Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Ukudeyeva A; Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Pine HS; Department of Otolaryngology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Campbell GA; Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Clement CG; Department of Pathology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
Case Rep Pathol ; 2018: 9814591, 2018.
Article em En | MEDLINE | ID: mdl-30410810
ABSTRACT

INTRODUCTION:

Plexiform schwannoma is a rare variant of schwannoma that accounts for only 5% of all schwannomas. Herein, we present a rare case of plexiform schwannoma of the tongue in a pediatric patient with neurofibromatosis type 2 (NF2). CASE PRESENTATION A 13-year-old female presented with a growing left-sided tongue mass. The patient has a past medical history of NF2. The tongue mass was excised and histopathological examination revealed a spindle cell tumor with multinodular growth pattern, with Verocay bodies' formation. Tumor cells were strongly positive for S-100 protein and negative for smooth muscle actin (SMA), and EMA highlighted perineural fibroblasts surrounding tumor nodules. These findings were diagnostic of plexiform schwannoma.

CONCLUSION:

Plexiform schwannoma of the tongue is an extremely rare tumor seen in patients with NF2. Clinical examination and histopathological evaluation are important for diagnosis of plexiform schwannoma.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article