Thyroid leiomyosarcoma: presentation of two cases and review of the literature.

Abstract:

INTRODUCTION:Leiomyosarcoma is a tumor which is rarely seen in the thyroid gland. The diagnosis may be difficult and the treatment is controversial. OBJECTIVE:The objective of the study is to review the literature about a rare malignant disease of the thyroid gland which has high mortality. METHODS:Two cases of thyroid leiomyosarcoma are presented and the previous 23 cases in the current literature are reviewed. RESULTS:A total of 25 cases of thyroid leiomyosarcoma are reviewed; the most common complaint was rapidly growing anterior neck mass, and ten of the 25 patients had distant metastasis at the initial admission. Fifteen of the 25 patients died with the disease in the first 12 months after the diagnosis. CONCLUSION:The differential diagnosis of thyroid leiomyosarcoma is important and should be performed with other malignancies of the gland, especially with anaplastic carcinoma. The prognosis is poor and there is no consensus regarding the treatment.

authors

Şahin Mİ,Vural A,Yüce İ,Çağlı S,Deniz K,Güney E

doi

10.1016/j.bjorl.2015.11.020

subject

Has Abstract

pub_date

2016-01-01 00:00:00

pages

715-721

issue

6

eissn

1808-8694

issn

1808-8686

pii

S1808-8694(16)30012-X

journal_volume

82

pub_type

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