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肋间肌海绵状血管瘤:胸壁的潘多拉魔盒。

Intercostal Muscle Cavernous Haemangioma: A Chest Wall Pandora's Box.

作者信息

Dantis Klein, Kashyap Yashwant, Raju Aghosh, Bhardwaj Swastik

机构信息

All India Institute of Medical Sciences, Raipur, India.

All India Institute of Medical Sciences, Bhopal, India.

出版信息

Eur J Case Rep Intern Med. 2021 Jan 27;8(1):002248. doi: 10.12890/2021_002248. eCollection 2021.

DOI:10.12890/2021_002248
PMID:33585348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7875575/
Abstract

BACKGROUND

Haemangiomas are uncommon chest wall tumours arising outside the rib cage. Their occurrence in intercostal muscle is extremely rare.

AIM

We describe a case of intercostal muscle cavernous haemangioma as a differential diagnosis for chest wall swelling.

CASE DESCRIPTION

We describe an 18-year-old male patient with an asymptomatic left-sided chest wall swelling. Contrast-enhanced computed tomography revealed a well-defined homogenously non-enhancing mass lesion arising from the seventh intercostal muscle with differential diagnoses of various chest wall tumours. Clinical presentation and imaging findings were inconclusive, but histopathological examination following excision biopsy revealed a cavernous haemangioma. The present case emphasizes the importance of histopathological diagnosis when clinical and radiological examination is inconclusive. Hence, it is necessary to consider intercostal muscle haemangiomas as a differential diagnosis for chest wall tumours in the absence of a feeding vessel.

CONCLUSION

Despite its rare occurrence, intercostal muscle haemangioma must be considered as a differential diagnosis in chest wall tumours even in the absence of a feeding vessel. We believe that histopathology can provide a definitive diagnosis when most investigative procedures are inconclusive.

LEARNING POINTS

Haemangiomas are rare chest wall tumours and even rarer when they originate from intercostal muscle.Intercostal muscle haemangiomas should be included in the differential diagnosis of chest wall tumours even in the absence of a feeding vessel.The present case emphasizes the importance of histopathological diagnosis when clinical and radiological examinations are inconclusive.

摘要

背景

血管瘤是起源于胸廓外的罕见胸壁肿瘤。它们发生于肋间肌极为罕见。

目的

我们描述一例肋间肌海绵状血管瘤病例,作为胸壁肿胀的鉴别诊断。

病例描述

我们描述一名18岁男性患者,左侧胸壁无症状肿胀。增强计算机断层扫描显示一个边界清晰、均匀无强化的肿块,起源于第七肋间肌,需与各种胸壁肿瘤进行鉴别诊断。临床表现和影像学检查结果不明确,但切除活检后的组织病理学检查显示为海绵状血管瘤。本病例强调了在临床和放射学检查不明确时组织病理学诊断的重要性。因此,在没有供血血管的情况下,有必要将肋间肌血管瘤作为胸壁肿瘤的鉴别诊断。

结论

尽管肋间肌血管瘤罕见,但即使没有供血血管,在胸壁肿瘤的鉴别诊断中也必须考虑到。我们认为,当大多数检查程序不明确时,组织病理学可以提供明确的诊断。

学习要点

血管瘤是罕见的胸壁肿瘤,起源于肋间肌时更为罕见。即使没有供血血管,肋间肌血管瘤也应纳入胸壁肿瘤的鉴别诊断。本病例强调了在临床和放射学检查不明确时组织病理学诊断的重要性。

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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.
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Materials and techniques in chest wall reconstruction: a review.胸壁重建的材料与技术:综述
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Intercostal hemangioma of the chest wall.胸壁肋间血管瘤
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