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乳腺侵袭性恶性血管球瘤:病例报告及文献复习。

Rapidly progressive malignant glomus tumor of the breast: a case report and review of the literature.

机构信息

Breast Center, West China Hospital of Sichuan University, Guoxuexiang Street, Chengdu, China.

Department of General Surgery, West China Hospital of Sichuan University, Guoxuexiang Street, Chengdu, China.

出版信息

J Int Med Res. 2024 Sep;52(9):3000605241272609. doi: 10.1177/03000605241272609.

DOI:10.1177/03000605241272609
PMID:39246065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11382221/
Abstract

The glomus tumor is a rare neoplasm that is typically found subungually in the extremities and functions as a specialized neurovascular organ. An extremely rare site for glomus tumors is the breast, with only a few reported cases. Breast glomus tumors present with three typical clinical signs: dull pain, focal tenderness, and cold sensitivity. Less than 10% of all glomus tumors are malignant. We herein present a case of a malignant glomus tumor originating in the breast. Distant metastasis was ruled out, and the tumor was completely resected. However, the patient unexpectedly developed rapid systemic metastasis, detected 5 weeks after tumor removal. Despite the administration of analgesics and targeted therapy, the patient died 1 month later. When treating patients with undiagnosed breast tumors, clinicians should pay attention to unexplained and repeatedly reported symptoms and consider the possibility of a rare disease. Our literature search revealed no cases of malignant glomus tumors originating in the breast, making this case the first of its kind.

摘要

血管球瘤是一种罕见的肿瘤,通常在四肢的指甲下发现,是一种特殊的神经血管器官。血管球瘤极为罕见的部位是乳房,仅有少数几例报道。乳房血管球瘤表现出三个典型的临床特征:钝痛、局部压痛和对冷敏感。不到 10%的血管球瘤是恶性的。本文报告了一例起源于乳房的恶性血管球瘤。排除了远处转移,并完全切除了肿瘤。然而,患者在肿瘤切除后 5 周意外发生快速全身转移。尽管给予了镇痛和靶向治疗,患者仍在 1 个月后死亡。当治疗原因不明的乳腺肿瘤的患者时,临床医生应注意不明原因和反复报告的症状,并考虑罕见疾病的可能性。我们的文献检索未发现起源于乳房的恶性血管球瘤病例,使本病例成为首例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de0/11382221/e7c5ace4859d/10.1177_03000605241272609-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de0/11382221/9614188400ba/10.1177_03000605241272609-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de0/11382221/e7c5ace4859d/10.1177_03000605241272609-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de0/11382221/9614188400ba/10.1177_03000605241272609-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de0/11382221/e7c5ace4859d/10.1177_03000605241272609-fig2.jpg

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本文引用的文献

1
Gastrointestinal Glomus Tumors: A Single Institution, 20-Year Retrospective Study.胃肠道血管球瘤:一项单机构20年回顾性研究
J Surg Res. 2023 Mar;283:982-991. doi: 10.1016/j.jss.2022.10.070. Epub 2022 Dec 10.
2
Combination of cardiac and carotid glomus tumour: a rare case report.心脏和颈动脉体瘤合并:一例罕见病例报告。
Folia Med (Plovdiv). 2022 Dec 31;64(6):1012-1015. doi: 10.3897/folmed.64.e67448.
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Glomus Tumors of the Distal Phalanx: A Retrospective Review of Clinical Diagnosis and Treatment.远端指骨血管球瘤:临床诊断和治疗的回顾性研究。
Orthopedics. 2022 Mar-Apr;45(2):e101-e106. doi: 10.3928/01477447-20220105-03. Epub 2022 Jan 12.
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Glomus tumour of the nipple in a male patient.男性患者的乳头血管球瘤。
Ann R Coll Surg Engl. 2022 Mar;104(3):e60-e63. doi: 10.1308/rcsann.2021.0141. Epub 2021 Nov 25.
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[Cardiac glomus tumor: An unusual localization of pericytic (perivascular) tumor].[心脏血管球瘤:一种不常见的周细胞(血管周)肿瘤定位]
Ann Pathol. 2021 Nov;41(6):561-566. doi: 10.1016/j.annpat.2021.06.007. Epub 2021 Oct 8.
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Extradural glomus tumor of the thoracic spine: case report and review of the literature.胸椎硬膜外球瘤:病例报告及文献复习。
Ann Palliat Med. 2021 Aug;10(8):9309-9317. doi: 10.21037/apm-21-1615. Epub 2021 Jul 29.
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Extradigital glomangiomyoma of the forearm mimicking peripheral nerve sheath tumour and thrombosed varicose vein.模仿周围神经鞘瘤和血栓形成的静脉曲张的前臂指外血管球瘤
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Gastric Glomus Tumor.胃血管球瘤
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"The unusual suspects"-Mammographic, sonographic, and histopathologic appearance of atypical breast masses.“不寻常的嫌疑人”-不典型乳腺肿块的乳腺摄影、超声和组织病理学表现。
Clin Imaging. 2020 Oct;66:111-120. doi: 10.1016/j.clinimag.2020.04.039. Epub 2020 May 3.
10
Low-Grade Malignancy Glomus Tumor in a Setting of Multiple Glomus Tumors - Case Report.多发性血管球瘤背景下的低级别恶性血管球瘤——病例报告
Open Access Maced J Med Sci. 2019 Dec 10;7(23):4082-4088. doi: 10.3889/oamjms.2019.610. eCollection 2019 Dec 15.