- Case report
- Open Access
- Open Peer Review
Giant fibrovascular polyp of the oesophagus: a case report and review of the literature
© Chourmouzi and Drevelegas; licensee BioMed Central Ltd. 2008
- Received: 03 March 2008
- Accepted: 28 October 2008
- Published: 28 October 2008
We present a case of fibrovascular polyp, a rare submucosal tumour of the oesophagus that has been reported only sporadically in the literature. The biapproach for surgical removal of fibrovascular polyp has only been mentioned once in the literature.
A 65-year-old Greek man presented with a 9-month history of gradually progressive intermittent dysphagia. Radiologic work-up with oesophagogram and computed tomography revealed a large, sausage-shaped intraluminal polyp extending from the level of the cervical oesophagus to the level of the upper body of the stomach. The diagnosis of giant fibrovascular polyp was made radiographically and confirmed by endoscopic biopsy. The polyp was removed using a biapproach surgical technique: pharyngotomy and subsequent gastrostomy.
Fibrovascular polyp is a rare submucosal tumour. Proper treatment depends on accurate assessment of the origin, size, and vascularity of the pedicle and the size of the tumour. Choice of the appropriate surgical approach depends on the correct diagnosis, which can usually be indicated radiographically by the presence of a smooth, sausage-shaped defect with a discrete bulbous tip.
- Endoscopic Resection
- Cervical Oesophagus
- Proximal Oesophagus
- Spindle Cell Carcinoma
A fibrovascular polyp (FVP) is a rare, benign, intraluminal, submucosal tumour-like lesion, characterised by the development of pedunculated, intraluminal masses that can exhibit enormous intraluminal growth. These lesions are composed of loose or dense fibrous tissue, adipose tissue, and vascular structures and are covered by normal squamous epithelium. The most common location is the upper third of the oesophagus, near the cricopharyngeus. Dysphagia, vomiting, weight loss, and respiratory symptoms are the most frequent complaints. However, long pedunculated lesions can regurgitate into the pharynx or mouth and cause death from asphyxiation if the larynx is occluded . We present a case of FVP associated with intermittent dysphagia.
A 65-year-old Greek man presented with a 9-month history of gradually progressive intermittent dysphagia. He also reported significant weight loss but no haemetemesis or melaena. The rest of his medical history was not significant. No specific abnormality was revealed during the physical examination.
CT with multiplanar reformatting provided valuable information regarding the location of the lesion as well as the size and anatomical attachment proximally, which was pivotal in directing surgery (Figure 2d). The intraluminal polyp showed soft tissue densities and a central area with attenuation identical to that of fat (Figure 2e). Endoscopy revealed a smooth submucosal mass occluding the oesophageal lumen. Endoscopic ultrasound-guided fine-needle aspiration was performed and cytological examination revealed benign fibro-fatty elements. The lesion was diagnosed as a submucosal FVP of the oesophagus, originating from the cervical oesophagus.
FVPs are rare submucosal tumours of the oesophagus almost always originating from the cervical oesophagus; they are benign but potentially life-threatening lesions. In the past, these lesions have been variably classified as 'lipomas', 'fibromas', and 'fibrolipomatous' polyps [2–5]. They usually arise in the proximal oesophagus behind the cricoid cartilage, frequently from the upper oesophageal sphincter. These polyps usually originate as small mucosal tumours just below the cricopharyngeus muscle sphincter, then extend into the oesophageal lumen by the constant downward urge of both food and peristalsis, and they may reach into the stomach [6, 7]. The incidence of these tumours is highest in middle-aged and elderly men, although some cases have occurred in children, infants, and women.
A FVP usually presents as a large, pedunculated lesion, and symptoms occur only once the polyp has become sufficiently large. Patients usually complain of dysphagia, substernal discomfort, and the sensation of a mass. Many cases of FVP have presented as regurgitated masses in the mouth, others have led to airway obstruction when the mass impacted on the larynx. Asphyxiation can result from impaction of the polyp in the glottis and is the most feared complication . Histologically, the lesion is composed of variable admixtures of mature adipose tissue lobules, collagenous and sometimes myxoid tissue, and prominent vasculature (a mixture of muscular arteries, thin-walled veins, and capillaries), all surrounded by mature squamous epithelium. Malignant degeneration of FVP is thought to be extremely rare.
Unless regurgitated, the presence of FVP can be difficult to diagnose, and patients may die without a correct diagnosis. FVPs can sometimes be identified during chest radiography by the presence of a right-sided superior mediastinal mass, anterior tracheal bowing, or both. At oesophagography, the lesion usually appears as a smooth, expansile intraluminal mass that arises in the cervical oesophagus and extends into the thoracic oesophagus. On CT scan, FVPs containing abundant adipose tissue may appear as soft-tissue-attenuated lesions (abundant fibrovascular tissue), with a paucity of fat, that expand the lumen of the oesophagus.
Although most FVPs have an attachment site in the cervical oesophagus, barium studies often fail to demonstrate a proximal pedicle. Accurate diagnosis is best established with endoscopy, although this technique is not completely reliable for diagnosing FVP. The differential diagnosis for FVP includes achalasia, extrinsic masses that compress the oesophagus, giant coalescent air bubbles, and other polypoid intraluminal tumours including lymphoma, spindle cell carcinoma, malignant melanoma, and leiomyosarcoma. The correct diagnosis can usually be suggested radiographically by the presence of a smooth, sausage-shaped defect with a discrete bulbous tip .
Removal of these lesions is usually recommended because of the progressive and eventually debilitating nature of the symptoms and the small but known risk of asphyxiation and sudden death. The most common therapeutic approach is surgical cervical oesophagostomy with complete excision of the stalk. The location of the stalk and the vascularity makes surgical resection the preferred mode for removing these unusual polyps. Endoscopic resection is possible but is generally avoided because of the potential for haemorrhage from the feeding vessels in the stalk. However, complication-free endoscopic resection of large oesophageal giant FVPs has been reported.
Generally, small polyps less than 2 cm in diameter and with a thin pedicle can be removed by endoscopic ligation and electrocoagulation of the pedicle. Polyps larger than 8 cm long or those with a thick, richly vascularised pedicle should be removed by surgical excision, and usually through a cervical incision. When the head of the polyp is too large to be removed through pharyngotomy, removal via gastrostomy is recommended. We could identify only one report in the literature about the surgical resection of FVP using the biapproach . A biapproach for surgical resection and removal of an FVP via pharyngotomy and gastrostomy is essential in cases of a large polyp that reaches into the stomach and has a bulbous distal tip.
Giant FVP of the oesophagus is a very rare entity and few reports on this lesion exist in the literature. Diagnosis can be difficult for physicians who are unfamiliar with this type of tumour. The most common location is the upper third of the oesophagus, near the cricopharyngeus. Dysphagia, vomiting, weight loss, and respiratory symptoms are the most frequent complaints. However, long pedunculated lesions can regurgitate into the pharynx or mouth and cause death from asphyxiation if the larynx is occluded. The details of our case should raise awareness for both radiologists and clinical physicians. Oesophagogram and CT are essential when evaluating a patient with such symptoms.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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