Ductal Adenocarcinoma Ex Pleomorphic Adenoma of the Lacrimal Gland: a Rare and Morbid Malignancy

Author:

Ashok Kumar Prashanth1ORCID,Paulraj Shweta1,Mirchia Kanish2ORCID,Hahn Seung Shin3,Sivapiragasam Abirami4

Affiliation:

1. Department of Internal Medicine, SUNY Upstate Medical University, Syracuse, NY 13210, USA

2. Department of Pathology, SUNY Upstate Medical University, Syracuse, NY 13210, USA

3. Department of Radiation Oncology, SUNY Upstate Medical University, Syracuse, NY 13210, USA

4. Department of Hematology-Oncology, SUNY Upstate Medical University, Syracuse, NY 13210, USA

Abstract

Carcinoma ex pleomorphic adenoma (Ca ex PA) is a rare malignant transformation of a benign primary pleomorphic adenoma (PA). We report the case of a 62-year-old male who presented with a swelling over his left temple. Imaging revealed a lytic lesion over the left orbital wall with soft tissue extension suggestive of malignancy. He underwent an en bloc resection of the mass with orbital exenteration, craniotomy, and reconstruction. Pathology demonstrated a lacrimal gland ductal adenocarcinoma arising from a PA which led to the diagnosis of ductal adenoCa ex PA. Postoperatively, he received chemotherapy with 6 cycles of cisplatin and concurrent radiation therapy (RT), but his course was complicated by recurrent bacterial meningitis and abscesses and he ultimately opted for comfort measures. Patients with PA of the lacrimal gland experience an insidiously enlarging painless swelling of the orbit with transformation to Ca ex PA highlighted by a rapid onset of bulbar enlargement, displacement, and often proptosis. Ductal adenoCa ex PA is aggressive with a poor prognosis and has no established standard of care. This case highlights the rarity of this condition and the need for more literature to help direct treatment.

Publisher

Hindawi Limited

Subject

Oncology

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