Volume 43, Issue 12 pp. 1186-1196
Case Report

Subcutaneous melanocytoma mimicking a lipoma: a rare presentation of a rare neoplasm with histological, immunohistochemical, cytogenetic and molecular characterization

Nitin Marwaha

Nitin Marwaha

Department of Pathology, Saint Louis University School of Medicine, St. Louis, MO, USA

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Jacqueline R. Batanian

Jacqueline R. Batanian

Department of Pathology, Saint Louis University School of Medicine, St. Louis, MO, USA

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Jeroen R. Coppens

Jeroen R. Coppens

Department of Neurosurgery, Saint Louis University School of Medicine, St. Louis, MO, USA

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Matthew J. Pierson

Matthew J. Pierson

Department of Neurosurgery, Saint Louis University School of Medicine, St. Louis, MO, USA

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Jennifer Richards-Yutz

Jennifer Richards-Yutz

Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, PA, USA

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Jessica Ebrahimzadeh

Jessica Ebrahimzadeh

Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, PA, USA

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Arupa Ganguly

Arupa Ganguly

Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, PA, USA

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Miguel A. Guzman

Corresponding Author

Miguel A. Guzman

Department of Pathology, Saint Louis University School of Medicine, St. Louis, MO, USA

Miguel A. Guzman, MD,

Department of Pathology, Saint Louis University School of Medicine, St. Louis, MO, USA

Tel: 314-577-5337

Fax: 314-268-6407

e-mail: [email protected]

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First published: 30 August 2016
Citations: 4

Abstract

Melanocytoma are the melanocytic tumors originating from leptomeningeal melanocytes. Melanocytomas are commonly seen in the central nervous system (CNS) and are often associated with neurocutaneous melanosis (NCM). However, simultaneous presentation of intra-axial and extracranial melanocytoma is a very rare event. Here, we report a unique case of 21-year-old male with intermediate-grade subcutaneous (SC) melanocytoma, mimicking lipoma, occurred synchronously with an intracranial melanocytoma, not associated with NCM. A 21-year-old Caucasian male presented to the emergency department (ED) with severe vertigo and vomiting. A magnetic resonance imaging (MRI) of the brain was performed at the ED, which revealed an SC mass in the right occipital scalp and a right cerebellopontine angle (CPA) mass. Excision of the SC mass revealed a well-circumscribed highly pigmented melanocytic tumor. The SC mass tumor cells were positive for melanocytic lineage markers. The histopathological features were between benign melanocytomas and malignant melanomas. The Ki67 and PHH3 IHCs confirm the intermediate grade of the tumors. An array-CGH (comparative genome hybridization) and next-generation sequencing analysis of the tumor DNA extracted from the formalin-fixed paraffin-embedded tissue reveals chromosome 6p gain and p.Q209P mutation in the GNAQ gene, respectively, consistent with the diagnosis of intermediate-grade melanocytoma.

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