Clinical Case Reports (Feb 2022)

Primary mucinous adenocarcinoma of the orbit: A rare clinical entity

  • Kais Maamri,
  • Rihab Ben Fredj,
  • Nesrine Nessib,
  • Amine Trifa,
  • Maher Hadhri,
  • Ghassen Elkahla,
  • Atef Ben Nsir,
  • Mehdi Darmoul

DOI
https://doi.org/10.1002/ccr3.5472
Journal volume & issue
Vol. 10, no. 2
pp. n/a – n/a

Abstract

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Abstract Primary mucinous adenocarcinoma is an exceptionally rare neoplasm with a propensity for local recurrence and metastasis. We report the second case in the world literature of a primary mucinous adenocarcinoma of the orbit in a 66‐year‐old man suffering from pain, progressive protrusion of left eye, and a deep drop in vision on the left for several weeks. His first external examination revealed significant proptosis with downward displacement of the left globe with no signs of lagophthalmos. A limitation of abduction was also noted. A CT of the orbit with and without contrast showed intra‐ and extra‐conical solid expansive process. MRI of the orbit with contrast and without contrast has shown a process of the supero‐internal angle of the left orbit. The patient was operated via a combined approach, and complete enucleation was done. The final pathologic diagnosis was mucinous adenocarcinoma of the orbit. The postoperative neuroimaging showed a complete resection of the tumor. The patient is referred for adjuvant radiotherapy. A CT of the orbit was made 3 months postoperatively and did not show any local recurrence.

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