甲状腺原发性平滑肌肉瘤
Primary Leiomyosarcoma of the Thyroid.
作者信息
Ben Kridis Wala, Sakka Dhouha, Saguem Ines, Charfeddine Ilhem, Daoud Jamel, Khanfir Afef
机构信息
Department of medical oncology, Habib Bourguiba Hospital, University of Sfax, Sfax, 3029, Tunisia.
Saguem pathology lab, Gabes, Tunisia.
出版信息
Head Neck Pathol. 2025 Jan 30;19(1):11. doi: 10.1007/s12105-024-01729-z.
Abstract
Leiomyosarcoma (LMS) is a malignant mesenchymal neoplasm showing smooth muscle differentiation. Primary LMS of the thyroid gland is quite rare, accounting for only 0.014% of cases. We report a case of a leiomyosarcoma arising in the right thyroid lobe of a 43-year-old man with complete remission following surgery, radiation therapy and chemotherapy.
摘要
平滑肌肉瘤（LMS）是一种表现出平滑肌分化的恶性间叶性肿瘤。甲状腺原发性平滑肌肉瘤相当罕见，仅占病例的0.014%。我们报告一例43岁男性右甲状腺叶发生的平滑肌肉瘤，经手术、放疗和化疗后完全缓解。
相似文献
1
Primary Leiomyosarcoma of the Thyroid.甲状腺原发性平滑肌肉瘤
Head Neck Pathol. 2025 Jan 30;19(1):11. doi: 10.1007/s12105-024-01729-z.
2
Comprehensive mutational profiling identifies new driver events in cutaneous leiomyosarcoma.全面的突变分析确定了皮肤平滑肌肉瘤中的新驱动事件。
Br J Dermatol. 2025 Jan 24;192(2):335-343. doi: 10.1093/bjd/ljae386.
3
Primary vaginal leiomyosarcoma: A case report emphasizing multidisciplinary care of a rare entity.原发性阴道平滑肌肉瘤：一例强调对罕见疾病进行多学科治疗的病例报告。
Radiol Case Rep. 2025 Jun 18;20(9):4444-4448. doi: 10.1016/j.radcr.2025.05.024. eCollection 2025 Sep.
4
Genomic characterization and histologic analysis of uterine leiomyosarcoma arising from leiomyoma with bizarre nuclei.伴有奇异核的平滑肌瘤来源子宫平滑肌肉瘤的基因组特征及组织学分析
J Pathol. 2025 Feb;265(2):211-225. doi: 10.1002/path.6379. Epub 2024 Dec 18.
5
Treatment for leiomyosarcoma and leiomyoma in children with HIV infection.感染艾滋病毒儿童的平滑肌肉瘤和平滑肌瘤的治疗。
Cochrane Database Syst Rev. 2010 May 12(5):CD007665. doi: 10.1002/14651858.CD007665.pub2.
6
Favorable response to nivolumab combined with radiotherapy for retroperitoneal leiomyosarcoma.
Int Cancer Conf J. 2025 May 16;14(3):190-197. doi: 10.1007/s13691-025-00771-0. eCollection 2025 Jul.
7
Demographic and Clinicopathological Analysis of Leiomyosarcoma at Various Anatomical Sites: A Tertiary Care Hospital Experience.不同解剖部位平滑肌肉瘤的人口统计学和临床病理分析：一家三级医疗中心的经验
Cureus. 2025 May 31;17(5):e85124. doi: 10.7759/cureus.85124. eCollection 2025 May.
8
Medullary Thyroid Cancer with Ectopic Cushing's Syndrome: A Case Report and Systematic Review of Detailed Cases from the Literature.《伴有异位库欣综合征的甲状腺髓样癌：病例报告及文献中详细病例的系统回顾》。
Thyroid. 2022 Nov;32(11):1281-1298. doi: 10.1089/thy.2021.0696. Epub 2022 Jul 12.
9
Intrathyroidal Parathyroid Carcinoma: Case Report and Literature Review.甲状腺内甲状旁腺癌：病例报告及文献综述
Ear Nose Throat J. 2025 Jan;104(1):30-35. doi: 10.1177/01455613221093729. Epub 2022 Apr 9.
10
Case Report: A dual challenge: navigating cardiac leiomyosarcoma and benign pulmonary mass.病例报告：双重挑战：应对心脏平滑肌肉瘤和肺部良性肿块。
Front Cardiovasc Med. 2025 Jun 10;12:1572673. doi: 10.3389/fcvm.2025.1572673. eCollection 2025.
本文引用的文献
1
Primary leiomyosarcoma of the thyroid gland: A rare case report and literature review.
Int J Surg Case Rep. 2024 Jun;119:109773. doi: 10.1016/j.ijscr.2024.109773. Epub 2024 May 17.
2
Primary leiomyosarcoma of the thyroid with concurrent papillary thyroid cancer: a rare case report and a review of literature.甲状腺原发性平滑肌肉瘤合并甲状腺乳头状癌：1例罕见病例报告及文献复习
Thyroid Res. 2023 Jun 5;16(1):16. doi: 10.1186/s13044-023-00157-5.
3
Primary Leiomyosarcoma of the Thyroid Gland - A Rare Malignancy.甲状腺原发性平滑肌肉瘤——一种罕见的恶性肿瘤。
Eur Endocrinol. 2019 Apr;15(1):44-46. doi: 10.17925/EE.2019.15.1.44. Epub 2019 Apr 12.
4
Thyroid leiomyosarcoma: presentation of two cases and review of the literature.甲状腺平滑肌肉瘤：两例病例报告及文献复习
Braz J Otorhinolaryngol. 2016 Nov-Dec;82(6):715-721. doi: 10.1016/j.bjorl.2015.11.020. Epub 2016 Mar 29.
5
Leiomyosarcoma of the thyroid: immunohistochemical and ultrastructural study.甲状腺平滑肌肉瘤：免疫组织化学和超微结构研究
Pathology. 1993 Apr;25(2):203-5. doi: 10.3109/00313029309084801.
Zotero 插件