Parathyroid Carcinosarcoma

Author:

Taggart James L.1,Summerlin Don-John2,Moore Michael G.3

Affiliation:

1. University of Washington, Seattle, WA, USA

2. Indiana University Health Pathology Laboratory, Indianapolis, IN, USA

3. Indiana University School of Medicine, Indianapolis, IN, USA

Abstract

Parathyroid carcinosarcoma was first described by Nacamuli et al in 2002. We present the second case of this rare disease. This rare carcinosarmoca presented as a parathyroid carcinoma with uncharacteristically normal parathyroid hormone levels. The patient is a 57-year-old woman with long-standing right-sided vocal cord paralysis presented with a progressive 3 × 2 × 3 cm mass in the right neck. She had previously undergone a total thyroidectomy revealing benign pathology. Parathyroid hormone and calcium blood levels were within normal limits. The mass was removed with negative surgical margins. Histopathology and immunohistochemical analysis showed a biphasic pattern, with positive for chromogranin and vimentin, consistent with carcinoma and sarcoma. The disease in our patient, as in the previously reported case, has shown systemic progression despite aggressive surgical resection and adjuvant therapy.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Case Report and Systematic Review: Sarcomatoid Parathyroid Carcinoma—A Rare, Highly Malignant Subtype;Frontiers in Endocrinology;2021-12-15

2. Malignant Neoplasms of the Parathyroid Gland;Head and Neck Pathology;2019

3. Parathyroid Pathology;Medical and Surgical Treatment of Parathyroid Diseases;2016-12-16

4. Thyroid and Parathyroid Glands;Pathology of the Head and Neck;2016

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