CASE REPORT |
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Year : 2020 | Volume
: 8
| Issue : 2 | Page : 75-79 |
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A case report of thyroid plasmacytoma and literature update
Fahd Refai1, Wafaey Gomaa2, Layla Abdullah1
1 Department of Pathology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia 2 Department of Pathology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Pathology, Faculty of Medicine, Minia University, Al Minia, Egypt
Correspondence Address:
Prof. Wafaey Gomaa Department of Pathology, Faculty of Medicine, King Abdulaziz University,
P.O. Box: 80205, Jeddah 21589, Saudi Arabia
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/JMAU.JMAU_36_19

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Plasmacytomas of the thyroid gland are rare, whether or not they arise as solitary (primary) lesions or secondary to systemic multiple myeloma. Here, we present the case of a 71-year-old female presenting with goiter and Hashimoto's thyroiditis, in whom the subsequent histopathological diagnosis of plasmacytoma was a surprise. In presenting this case, we summarize the last 25 years of literature on thyroid plasmacytoma and review the salient clinicopathological characteristics, differential diagnoses, management, and outcomes of this rare condition.
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