Choked for Over a Decade: A Rare Case of Huge Esophageal Fibro-vascular Polyp Causing Dysphagia

S. Kassa, D. Ayalew
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Abstract

Introduction: Esophageal fibro-vascular polyps (EFVPs) are rare benign tumors that can arise from the submucosa of the esophagus. They are usually asymptomatic but can cause obstruction and dysphagia in some cases. The diagnosis of EFVPs can be challenging due to their rarity and nonspecific symptoms. Delayed diagnosis can result in significant morbidity, as in the case of our patient who suffered from difficulty swallowing for over a decade before being accurately diagnosed. We present a case of a 42-year-old male patient with a 12-year history of difficulty swallowing, who was eventually diagnosed with a huge fibro-vascular polyp after undergoing thoracotomy esophagostomy and excision of the polyp. Case Presentation: A 42-year-old male patient presented to Hallelujah General Hospital, with a 12-year history of difficulty swallowing, associated with symptoms such as weight loss, fatigue, and asphyxiation while vomiting. The patient had visited several health centers but was unable to receive an accurate diagnosis or effective treatment. Initial investigations revealed a large, smooth, and mobile mass in the mid-esophagus, which was obstructing the lumen and causing difficulty swallowing. A CT scan of the chest and abdomen showed a large polypoid mass in the upper and mid-esophagus, measuring 25 cm in length and 10 cm in diameter, which was confirmed to be an esophageal fibro-vascular polyp upon surgical excision and biopsy. Conclusion: EFVPs are rare, benign tumors of the esophagus that can cause significant morbidity if not diagnosed and treated promptly. The diagnosis of EFVPs can be challenging, and imaging studies such as CT scans, MRI, and endoscopic ultrasound can be helpful in diagnosing the condition. However, a definitive diagnosis usually requires histological examination of the excised mass. Surgical excision is the treatment of choice for EFVPs, and the prognosis is usually excellent. This case report highlights the importance of considering rare conditions in the differential diagnosis of common symptoms, particularly if the patient does not respond to initial treatment. It also emphasizes the importance of early diagnosis and prompt surgical intervention in preventing complications and improving outcomes for patients with EFVPs.
窒息十多年:罕见的巨大食道纤维血管息肉导致吞咽困难
食管纤维血管息肉(EFVPs)是一种罕见的良性肿瘤,可起源于食管粘膜下层。它们通常无症状,但在某些情况下可引起梗阻和吞咽困难。由于其罕见和非特异性症状,EFVPs的诊断可能具有挑战性。延迟诊断可能导致严重的发病率,就像我们的病人在被准确诊断之前遭受吞咽困难超过十年。我们报告一例42岁的男性患者,有12年的吞咽困难病史,在接受开胸食管造口术并切除息肉后,最终被诊断为巨大的纤维血管息肉。病例介绍:一名42岁男性患者在哈利路亚总医院就诊,有12年的吞咽困难史,伴有体重减轻、疲劳和呕吐时窒息等症状。该患者曾去过几个保健中心,但未能得到准确的诊断或有效的治疗。初步检查发现食管中部有一个大的、光滑的、可移动的肿块,阻塞了管腔,导致吞咽困难。胸部及腹部CT示食道上部及中段一大息肉样肿块,长25cm,直径10cm,经手术切除及活检证实为食道纤维血管息肉。结论:EFVPs是一种罕见的食管良性肿瘤,如果不及时诊断和治疗,可能会导致严重的发病率。EFVPs的诊断可能具有挑战性,CT扫描、MRI和内窥镜超声等影像学研究可以帮助诊断这种疾病。然而,明确的诊断通常需要对切除的肿块进行组织学检查。手术切除是EFVPs的治疗选择,预后通常很好。本病例报告强调了在鉴别诊断常见症状时考虑罕见病的重要性,特别是当患者对初始治疗无反应时。它还强调了早期诊断和及时手术干预在预防并发症和改善efvp患者预后方面的重要性。
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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