A rare case of leptomeningeal carcinomatosis in a patient with uveal melanoma: case report and review of literature

Melanoma Res. 2016 Oct;26(5):481-6. doi: 10.1097/CMR.0000000000000274.

Abstract

Uveal melanoma is a rare subtype of melanoma, accounting for only 3-5% of all melanoma cases in the USA. Although fewer than 4% of uveal melanoma patients present with metastasis at diagnosis, approximately half will develop metastasis, more than 90% of which disseminate to the liver. Infrequently, a number of malignancies can lead to leptomeningeal metastases, a devastating and terminal complication. In this case report, we present an exceedingly rare case of a patient with uveal melanoma who developed leptomeningeal carcinomatosis as the sole site of metastasis. After conventional methods to diagnose leptomeningeal carcinomatosis fell short, a diagnosis was confirmed on the basis of identification and genomic analysis of melanoma circulating tumor cells in the cerebrospinal fluid.

Publication types

  • Case Reports
  • Review
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Female
  • Humans
  • Melanoma / complications*
  • Melanoma / pathology
  • Meningeal Carcinomatosis / etiology*
  • Middle Aged
  • Skin Neoplasms / complications*
  • Skin Neoplasms / pathology
  • Uveal Neoplasms / complications*
  • Uveal Neoplasms / pathology

Supplementary concepts

  • Uveal melanoma