Melanoma Mimicking Malignant Peripheral Nerve Sheath Tumor with Spread to the Cerebellopontine Angle: Utility of Next-Generation Sequencing in Diagnosis

Author:

Fox Hanson Katie1,Birinyi Paul2,Walker Ronald3,Raptis Constantine4,Chernock Rebecca5,Coppens Jeroen6,Schwetye Katherine E.1ORCID

Affiliation:

1. Department of Pathology, Saint Louis University School of Medicine, 1402 S. Grand Blvd., St. Louis, MO 63104, USA

2. University of Tennessee Health Science Center, Department of Neurosurgery/Semmes-Murphey Clinic, USA

3. Department of Otolaryngology, Saint Louis University School of Medicine, 1402 S. Grand Blvd., St. Louis, MO 63104, USA

4. Mallinckrodt Institute of Radiology, Washington University School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110, USA

5. Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110, USA

6. Department of Neurosurgery, Saint Louis University School of Medicine, 1402 S. Grand Blvd., St. Louis, MO 63104, USA

Abstract

Cutaneous spindle cell malignancy is associated with a broad differential diagnosis, particularly in the absence of a known primary melanocytic lesion. We present an unusually challenging patient who presented with clinical symptoms involving cranial nerves VII and VIII and a parotid-region mass, which was S100-positive while lacking in melanocytic pigment and markers. Over a year after resection of the parotid mass, both a cutaneous primary lentigo maligna melanoma and a metastatic CP angle melanoma were diagnosed in the same patient, prompting reconsideration of the diagnosis in the original parotid-region mass. Next-generation sequencing of a panel of cancer-associated genes demonstrated 19 identical, clinically significant mutations as well as a high tumor mutation burden in both the parotid-region and CP angle tumors, indicating a metastatic relationship between the two and a melanocytic identity of the parotid-region tumor.

Publisher

Hindawi Limited

Subject

General Medicine

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