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肋间肌内血管瘤的诊断和治疗:最新综述。

Diagnosis and management of intercostal intramuscular hemangioma: an updated review.

机构信息

Department of Thoracic Surgery, Tokyo Women's Medical University Yachiyo Medical Center, 477-96, Owada-Shinden, Yachiyo, 276-8524, Chiba, Japan.

Department of Pathology, Tokyo Women's Medical University Yachiyo Medical Center, 477-96, Owada-Shinden, Yachiyo, 276-8524, Chiba, Japan.

出版信息

J Cardiothorac Surg. 2023 Jul 4;18(1):210. doi: 10.1186/s13019-023-02328-9.

Abstract

BACKGROUND

Intramuscular hemangioma (IMH) is an uncommon type of hemangioma, and primary IMH of the intercostal muscle is even rarer. Only a few reports describe IMH of the intercostal muscle, and there are no review articles on this topic. We report our experience with a younger female patient, who underwent video-assisted thoracic surgery with tumor resection and review the previous literatures of intercostal IMH.

CASE PRESENTATION

An asymptomatic 17-year-old woman showed a 29-mm, homogeneous, intrathoracic nodule in the left chest wall, attached to the second and third ribs on computed tomography. We performed exploratory thoracoscopic surgery and the tumor was excised without surrounding rib resection. Histopathologic examination of the surgical specimen revealed proliferation of small blood vessels within the surrounding striated muscle, leading to the diagnosis of intercostal IMH. The surgical margin was negative. The patient's postoperative course was uneventful, and there has been no evidence of recurrence for more than 18 months after surgery.

CONCLUSIONS

We describe a case of intercostal IMH, who received tumor resection with clear excision margin without surrounding rib resection. Preoperative diagnosis is challenging due to its rarity, but intercostal IMH should be recalled as a differential diagnosis of chest wall tumor. Tumor excision without surrounding rib resection is acceptable for intercostal IMH, when there is a good possibility of achieving negative surgical margin.

摘要

背景

肌间血管瘤(IMH)是一种罕见的血管瘤类型,而肋间肌原发性 IMH 则更为罕见。仅有少数文献报道了肋间肌 IMH,且尚无关于该主题的综述文章。我们报告了一位年轻女性患者的病例,该患者接受了电视辅助胸腔镜手术(VATS)进行肿瘤切除,并回顾了之前关于肋间 IMH 的文献。

病例介绍

一位无症状的 17 岁女性在左胸壁显示出一个 29mm、均匀的、位于胸腔内的结节,附着在第二和第三肋骨上。我们进行了探索性胸腔镜手术,切除了肿瘤而未切除周围肋骨。手术标本的组织病理学检查显示周围横纹肌内小血管的增殖,导致诊断为肋间 IMH。手术切缘阴性。患者术后恢复顺利,手术后 18 个月以上无复发迹象。

结论

我们描述了一例肋间 IMH 患者,该患者接受了肿瘤切除术,切缘清晰,未切除周围肋骨。由于其罕见性,术前诊断具有挑战性,但肋间 IMH 应作为胸壁肿瘤的鉴别诊断之一。当有很大可能获得阴性手术切缘时,肋间 IMH 无需切除周围肋骨即可接受肿瘤切除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e6/10318703/59e44138afd3/13019_2023_2328_Fig1_HTML.jpg

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本文引用的文献

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Intercostal Muscle Cavernous Haemangioma: A Chest Wall Pandora's Box.肋间肌海绵状血管瘤:胸壁的潘多拉魔盒。
Eur J Case Rep Intern Med. 2021 Jan 27;8(1):002248. doi: 10.12890/2021_002248. eCollection 2021.
5
Intercostal hemangioma: Case report of a rare chest wall tumor in childhood.肋间血管瘤:儿童罕见胸壁肿瘤病例报告
Int J Surg Case Rep. 2019;60:319-322. doi: 10.1016/j.ijscr.2019.06.026. Epub 2019 Jun 20.
6
Giant cavernous hemangioma of the eleventh rib.第十一肋巨大海绵状血管瘤
J Cardiothorac Surg. 2019 May 22;14(1):95. doi: 10.1186/s13019-019-0919-6.
7
Extraordinary Presentation of Elastofibroma Dorsi After a Thoracotomy Procedure.胸外科手术后背部弹力纤维瘤的特殊表现。
J Natl Med Assoc. 2018 Oct;110(5):428-430. doi: 10.1016/j.jnma.2017.09.005. Epub 2017 Nov 2.
8
Desmoid fibromatosis of the chest wall.胸壁韧带样纤维瘤病
Respirol Case Rep. 2018 Feb 28;6(4):e00310. doi: 10.1002/rcr2.310. eCollection 2018 May.
10
Primary Hemangiomatous Tumors of Skeletal Muscle.骨骼肌原发性血管瘤样肿瘤
Ann Surg. 1944 May;119(5):700-40. doi: 10.1097/00000658-194405000-00006.

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