Ectopic carcinoma ex-pleomorphic adenoma in the lower neck: a rare entity at a rare location

Authors

  • Kuganathan Ramasamy Department of Otorhinolaryngology-Head & Neck Surgery, Hospital Tuanku Ja’afar, Seremban, Negeri Sembilan, Malaysia
  • Yatiee Swany Lahuri Department of Otorhinolaryngology-Head & Neck Surgery, Hospital Tuanku Ja’afar, Seremban, Negeri Sembilan, Malaysia
  • Norhaslinda Abdul Gani Department of Otorhinolaryngology-Head & Neck Surgery, Hospital Tuanku Ja’afar, Seremban, Negeri Sembilan, Malaysia
  • Noor Hasni Shamsudin Department of Pathology, Hospital Tuanku Ja’afar, Seremban, Negeri Sembilan, Malaysia

DOI:

https://doi.org/10.3329/bjms.v20i3.52812

Keywords:

Carcinoma ex-pleomorphic adenoma; pleomorphic adenoma; ectopic salivary gland; neck

Abstract

Ectopic salivary gland tissue (ESGT) is salivary tissue located outside the major, minor and accessory salivary glands. Neoplasms rarely arise from ESGT, let alone carcinoma expleomorphic adenoma (CEPA) which is a malignant tumour that arises from the epithelial component of pleomorphic adenoma. It usually occurs in the parotid gland and in lesser instances, from submandibular gland or minor salivary glands. Herein, we report a rare case of CEPA in right supraclavicular ESGT of a 67-year-old lady.She underwent complete surgical excision of the mass and is free from any recurrence to date. Brief review of pathogenesis, clinical features and treatment of ectopic CEPA are discussed. A thorough review of the English literature reveals that our patient may be the second case of ectopic CEPA in the neck region ever reported to date.

Bangladesh Journal of Medical Science Vol.20(3) 2021 p.658-661

Downloads

Download data is not yet available.
Abstract
23
PDF
42

Downloads

Published

2021-04-04

How to Cite

Ramasamy, K., Lahuri, Y. S., Gani, N. A., & Shamsudin, N. H. (2021). Ectopic carcinoma ex-pleomorphic adenoma in the lower neck: a rare entity at a rare location. Bangladesh Journal of Medical Science, 20(3), 658–661. https://doi.org/10.3329/bjms.v20i3.52812

Issue

Section

Case Reports