Combined Schwannoma and Kappa-Restricted Plasma Cell Neoplasm: A Case Report and Review of the Literature

Author:

Cannatella Jeffrey John1,Pandey Soumya2ORCID

Affiliation:

1. Department of Pathology, University of Nebraska Medical Center, 983135 Nebraska Medical Center, Omaha, NE 68106-3135, USA

2. Department of Pathology, University of Arkansas for Medical Sciences, 4301 West Markham Street, Mail Slot 502, Little Rock, AR 72205, USA

Abstract

The patient is a 78-year-old woman with a popliteal soft tissue mass that was tender to palpation with shooting pain on physical examination. A schwannoma was seen on biopsy with subsequent excision demonstrating a concomitant kappa-restricted plasma cell neoplasm. Follow-up did not show evidence of a systemic plasma cell neoplasm. MRI studies showed no evidence of focal lesions, although PET-CT revealed presence of multiple lytic lesions. The patient is currently being monitored every six months. This case is the first kappa-restricted plasma cell neoplasm reported in association with a schwannoma and the first reported in the extremities.

Publisher

Hindawi Limited

Subject

General Medicine

Reference12 articles.

1. Benign soft-tissue tumors in a large referral population: distribution of specific diagnoses by age, sex, and location.

2. Tumour stem cells in schwannoma: A review

3. Universal absence of merlin, but not other ERM family members, in schwannomas;A. O. Stemmer-Rachamimov;The American Journal of Pathology,1997

4. Plasma Cell Neoplasms;R. W. McKenna,2017

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