Tracheal Lobular Capillary Hemangioma: A Rare Localization.

Q3 Medicine
Tanaffos Pub Date : 2023-04-01
Sarra Maazaoui, Nouha Boubaker, Islam Mejri, Sonia Habibech, Amany Touil, Mouna Mlika, Hajer Racil, Zied Moatemri, Faouzi El Mezni, Nawel Chaouch
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引用次数: 0

Abstract

Background: Lobular capillary hemangioma is a benign vascular tumor commonly found within the skin and upper respiratory mucosa and has rarely been reported within the trachea. The first case was reported by Irani et al. in 2003 and since then, less than 20 cases have been described. That's why the characteristics and treatments remain relatively unknown.

Case presentation: A 53-year-old woman was symptomatic of recurrent episodes of hemoptysis associated with paroxysmal dyspnea. Physical examination, routine blood investigations, and chest x-ray were normal. The flexible bronchoscopy showed a polypoid bleeding lesion arising from the right lateral wall of the middle third of the trachea. Tumor biopsy was not performed considering an eventual bleeding risk. Computed tomography scanning showed a vascular, endotracheal budding tissue process without peritracheal or distant extension. A rigid bronchoscopy was performed for diagnostic and therapeutic purposes. A 10-millimeter bronchoscope was used. A rigid coring technique was performed to remove the tumor. A minimal bleeding was completely controlled after diode laser treatment. There were no complications during or after the procedure. Pathology revealed no malignancy and the diagnosis of lobular capillary hemangioma was confirmed. At a 6-month follow-up, the patient was asymptomatic and the endoscopic control did not show any tumor recurrence.

Conclusion: The lobular capillary hemangioma is a benign tumor rarely observed in the trachea. Clinical features are not specific and the short-term prognosis depends on tumor size. Considering its benign nature, tumor removal by interventional bronchoscopy should be proposed as the first-line treatment.

气管叶状毛细血管瘤:罕见的定位
背景:叶状毛细血管瘤是一种良性血管肿瘤,常见于皮肤和上呼吸道粘膜,在气管内很少见报道。2003 年,Irani 等人报告了第一例,自此以后,描述的病例不到 20 例。因此,该病的特征和治疗方法仍相对未知:病例介绍:一名 53 岁女性的症状是反复发作的咯血并伴有阵发性呼吸困难。体格检查、常规血液检查和胸部 X 光检查均正常。柔性支气管镜检查显示,气管中三分之一处的右侧壁出现息肉样出血病变。考虑到最终的出血风险,没有进行肿瘤活检。计算机断层扫描显示,肿瘤为血管性气管内芽组织过程,无气管周围或远处扩展。出于诊断和治疗目的,对患者进行了硬质支气管镜检查。使用的是 10 毫米支气管镜。采用硬质取芯技术切除肿瘤。二极管激光治疗后,少量出血得到完全控制。术中和术后均未出现并发症。病理检查未发现恶性肿瘤,确诊为小叶毛细血管瘤。在6个月的随访中,患者无任何症状,内窥镜检查也未发现肿瘤复发:结论:小叶毛细血管瘤是气管中很少见的良性肿瘤。结论:小叶毛细血管瘤是气管中很少见的良性肿瘤,临床特征不具特异性,短期预后取决于肿瘤的大小。考虑到其良性性质,应将介入性支气管镜切除肿瘤作为一线治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tanaffos
Tanaffos Medicine-Critical Care and Intensive Care Medicine
CiteScore
1.10
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0.00%
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