Mahdjoubi Amir, Cassoux Nathalie, Levy-Gabriel Christine, Desjardins Laurence, Klos Jan, Caly Martial, Vlajnic Tatjana, Gardrat Sophie, Klijanienko Jerzy
Department of Ophtalmology, Institut Curie 26, Rue d'Ulm, 75248, Paris Cedex, France.
Department of Pathology, Institut Curie 26, Rue d'Ulm, 75248, Paris Cedex, France.
Diagn Cytopathol. 2017 Jun;45(6):561-564. doi: 10.1002/dc.23694. Epub 2017 Feb 20.
Ocular medulloepithelioma (ME) is a rare congenital tumor which occurs usually during childhood but is also reported in adults. They have seen an intraocular tumor in an 89 years-old female with a history of small cell lung carcinoma. Transscleral fine needle aspiration was performed. Aspirates were rich and composed of two distinctive populations of cells. The first consisted of epithelioid large cohesive cells with rare rosettes. Nuclei were oval and chromatin was delicate with small nucleoli. The second population consisted of smaller and dispersed cells with regular nuclei and dusty chromatin. Immunohistochemistry performed on paraffin-embedded cell block sections showed that the larger cells and rosettes were cytokeratin AE1/AE3, Synaptophysin, Chromogranin A, CD56, NSE, and EMA positive, whereas the smaller cells were always negative. Interestingly smaller cells expressed only weak nuclear positivity for TTF1, whereas larger cells were TTF1 negative. Melanocytic markers were negative in both populations. Morphological patterns and immunohistochemical staining confirmed ocular ME and allowed to exclude pulmonary metastasis or primary malignant melanoma. The patient was successfully treated by brachytherapy alone and is alive and well 10 months after treatment. Diagn. Cytopathol. 2017;45:561-564. © 2017 Wiley Periodicals, Inc.
