Open Access

Giant fibrovascular polyp in the hypopharynx: a case report and review of the literature

SpringerPlus20165:1443

https://doi.org/10.1186/s40064-016-3144-y

Received: 1 June 2016

Accepted: 24 August 2016

Published: 30 August 2016

Abstract

Introduction

Fibrovascular polyps (FVPs) are benign tumors that commonly occur in the cervical esophagus. Few cases of FVPs of the hypopharynx have been reported, but there has been no English review concerning hypopharyngeal FVPs (hFVPs). Here, we report a case of a vast hFVP, and we also review 13 hFVP cases found in the English literature (PubMed search) including our case.

Case description

A 41-year-old man with respiratory distress and regurgitation of a mass was referred to our hospital. Endoscopic and radiographic evaluations were required for diagnosis. The tumor originated from the hypopharynx and covered almost the entire larynx, which caused the airway to narrow. An emergency surgical removal was performed under general anesthesia with orotracheal intubation, and the tumor was completely removed transorally using a laryngeal endoscope. Pathological examination revealed that the mass was a FVP.

Discussion and Evaluation

We investigated patient characteristics, symptoms, polyp size, treatments, and recurrence of 13 hFVP cases. Regurgitation of a mass, dyspnea, and dysphagia were frequently reported symptoms at presentation. All patients were treated by surgical excision with no recurrence. Airway management is critical and tracheotomies were needed in some cases.

Conclusions

FVPs are often asymptomatic, and they can suddenly cause respiratory distress from laryngeal blockage. Therefore, we emphasize that when such cases are encountered, airway management and surgical treatment should be considered as early as possible.

Keywords

Fibrovascular polypHypopharynxDyspneaSurgical treatmentAirway management

Introduction

Fibrovascular polyps (FVPs) are rare benign tumors of the upper digestive tract, and they account for approximately 1 % of all benign tumors in the esophagus and hypopharynx (Avezzano et al. 1990; Sargent and Hood 2006). Most FVPs are located in the cervical very rare (Kim and Shim 2006), and there has been no English review concerning hypopharyngeal FVPs (hFVPs). Most patients are completely asymptomatic, but in some cases, dysphagia, dyspnea, and specifically regurgitation of a mass into the oral cavity may occur. In addition, sudden asphyxia from laryngeal blockage can also occur (Sargent and Hood 2006). Surgical removal is recommended for this disease.

We encountered an extremely rare case of a vast hFVP that caused dyspnea, and we reviewed 13 hFVP cases that have been reported in the English literature, including our case, to verify hFVP characteristics and treatment.

Case description

A 41-year-old man with no previous medical history was referred to the University of Tokyo Hospital owing to sudden respiratory distress caused by regurgitation of a tumor following vomiting after alcohol intake. A dull, red tumor was protruding from his mouth (Fig. 1), he was experiencing dyspnea in the dorsal position, and his speech was slurred. Endoscopic examination showed a tumor originating in the right hypopharynx and covering almost the entire larynx. The tumor caused almost complete airway obstruction (Fig. 2). Computed tomography (CT) scans showed that the tumor occupied the oral cavity to the esophagus. T2-weighted magnetic resonance imaging (MRI) showed that the tumor had a high-intensity area (Fig. 3). To secure a clear airway, we performed an emergency surgical removal. Orotracheal intubation was successfully performed with endoscopic assistance. Using a Weerda laryngoscope, we could distinctly view the hypopharynx. A pedunculated, soft-tissue tumor originated from the posterior wall of the right hypopharynx, and two branched ends extended into the mouth and thoracic esophagus. We performed a transoral excision completely via laryngeal endoscopy. The body of the tumor was smooth and dark red-brown color, and the two, branched ends of the tumor measured 12 and 8 cm, respectively (Fig. 4). Microscopically, the polyp consisted of a fibro-adipose tissue and blood vessels covered with normal squamous cell epithelium (Fig. 5). Histopathological diagnosis of the tumor revealed a typical FVP. After operation, the dyspnea disappeared. His swallowing function was very good by video-fluorography four days after operation, and he restarted oral intake. The patient recovered with no problems and was discharged eight days after surgery. He has no recurrence in 4 years of follow-up.
Fig. 1

A giant fibrovascular polyp in the mouth (arrow)

Fig. 2

Endoscopic views of the polyp. a, b: A large polyp (asterisks) with two branches from the right hypopharynx on the base of tongue (arrow in a) covered almost the entire larynx and caused airway narrowing (arrow in b)

Fig. 3

Radiological findings. a, b: Contrast-enhanced computed tomography scans revealed that the tumor (arrow) occupied the oral cavity to the esophagus (a axial, b sagittal). c, d: T2-weighted magnetic resonance imaging revealed a high-intensity area within the tumor (arrow) (c axial, d sagittal)

Fig. 4

Histological findings. A forked fibrovascular polyp, with branched ends measuring 12 and 8 cm, respectively, was removed

Fig. 5

Microscopic findings. The polyp consisted of fibro-adipose tissues (white arrows) and blood vessels (gray arrows) covered by normal squamous cell epithelium (black arrows). Magnification,  × 20; Hematoxylin-eosin stain

Discussion and Evaluation

More than 100 cases of FVP have been previously reported, but there are few cases arising from hypopharynx and there has been no English review of hFVPs. We searched the PubMed database using two keywords, “fibrovascular polyp” and “hypopharynx”. The search resulted in nine publications (Owens et al. 1994; Nuyens et al. 2004; Zevallos et al. 2005; Kim and Shim 2006; Al-Swiahb and Al-Dousary 2008; Ozdemir et al. 2011; Wang et al. 2011; Pallabazzer et al. 2013; Haytoglu et al. 2015) that included 12 cases in English. We included the case we experienced, and 13 cases in total were reviewed. We investigated patient characteristics, symptoms, polyp size, treatments, and recurrence.

Table 1 shows the details of hFVP for 13 cases. Analysis of available data demonstrated that hFVPs occur with a male to female ratio of 9–4. The mean age at diagnosis was 56 years, with a range of 31–80 years. Almost all patients experienced regurgitation of a mass, and dysphagia was the second most frequent symptom, occurring in 54 % of patients. Dyspnea was also detected in one-third of cases. Other symptoms were reported as follows: vomiting (31 %), laryngeal discomfort (23 %), weight loss (15 %), syncope (8 %), anemia (8 %), and sore throat (8 %). Surgical excision was performed in all cases, and transoral approaches were used in the majority of these cases. Tracheotomy was required in 3 cases (23 %), due to laryngeal obstruction by the regurgitated mass. The mean polyp length was 12 ± 6.2 cm. In four cases, the hFVPs were larger than the 12 cm polyp in our case. In 3 of these cases, pharyngotomy or gastrotomy was used to remove the entire tumor. Recurrence has not occurred after resection in these cases.
Table 1

Literature review of hFVPs (n = 13)

Sex (male: female)

9: 4

Age

56 years; (range 31–80)

Tumor size

12 ± 6.2 cm

 

Number of cases

Frequency (%)

Symptom

  

Regurgitation of a mass

11

85

Dysphagia

7

54

Dyspnea

5

38

Vomiting

4

31

Laryngeal discomfort

3

23

Weight loss

2

15

Syncope

1

8

Anemia

1

8

Sore throat

1

8

Surgical approach

  

Trans-oral (endoscopic/laryngoscopic)

7 (1/6)

54

Trans-cervical

5

38

Gastrotomy

1

8

Tracheotomy

3

23

Recurrence

0

0

FVPs are rare benign tumors of the upper digestive tract that are rarely encountered in clinical practice. Approximately one-third of large pedunculated polyps (>5 cm) originating in the esophagus and hypopharynx are FVPs (Caceres et al. 2006). Whereas esophageal FVPs are commonly diagnosed in the sixth or seventh decade of life, with the exception of an infant with FVP (Paik et al. 2001), the mean age at hFVP diagnosis was 56 years in the present study. These tumors are reportedly more frequent in males (male: female ratio = 3:1) (Paik et al. 2001), and our review of hFVPs confirmed these data (male: female ratio = 9:4). About 85 % of FVPs are located in the cervical esophagus (Kim and Shim 2006). In addition, rare cases arising from the oropharynx, larynx, or stomach have also been reported (Caceres et al. 2006; Lee et al. 2013; Nascimento et al. 2014; Gupta et al. 2011). Their exact etiologies are not well known. FVPs usually originate as small mucosal tumors adjacent to the cricopharyngeal muscle, and they slowly extend into the esophageal lumen due to the constant downward thrust by food ingestion and peristalsis, sometimes growing to reach the gastric cavity (Kim and Shim 2006). FVPs usually occur as solitary lesions. A case of synchronous hFVPs has been reported (Nuyens et al. 2004), but no previous patient has been described with a forked polyp with two-branches in the hypopharynx as seen in the patient from the present case. Malignant transformation and recurrence for these polyps are reportedly rare, despite some reported cases of recurrence (Lee et al. 2009).

FVPs may remain asymptomatic for many years because of their slow growth. Common symptoms of large FVPs include dysphagia, respiratory distress, and regurgitation of a mass in the oral cavity, which is the most specific symptom that carries risk of aspiration into the airways, resulting in asphyxia (Caceres et al. 2006). In our review, almost all patients experienced regurgitation of a mass, and it is difficult to diagnose FVP without this characteristic symptom. Although there have been reports of sudden death from asphyxiation after regurgitation of a tumor and up to 30 % of patients may die without a correct diagnosis (Timmons et al. 1991), the patient in this case fortunately lived. Various symptoms like laryngeal discomfort, weight loss, and anemia, are observed in patients with FVP.

FVPs can be visualized by endoscopic examination. CT scans and MR imaging can be useful in confirming diagnostic suspicions and in deciding the proper surgical approach. Histologically, polyps are covered by normal squamous epithelium, consisting of adipose and connective tissue, and a well-developed vascular network. The differential diagnosis of FVPs includes leiomyoma, neurofibroma, hemangioma, fibrolipoma, fibromyxoma, hamartoma, fibroma, lipoma, and schwannoma as well as several rare neoplasms, such as carcinoid tumor and chemodectoma (Timmons et al. 1991; Caceres et al. 2006).

Tumor excision is the only treatment for FVP. Sudden asphyxia may occur due to this tumor, and thus, surgical treatment is required as soon as possible after encountering this tumor. Other reasons for excision include the possibility of malignancy and symptomatic improvement. Use of transoral approaches (endoscopic or laryngoscopic) and surgical approaches (transcervical or transthoracic) depend on the FVP location, pedicle vascularity, and size. Identification of the polyp’s pedicle is very important for successful removal of the tumor. Small polyps that are less than 2 cm in diameter with thin pedicles may be removed by the transoral approach. Polyps larger than 8 cm in length or those with thick, richly vascularized pedicles should be removed by surgical excision through a cervical or thoracic approach (Kim and Shim 2006; Wang et al. 2011). However, as shown in the present report, we could successfully remove the tumor by the transoral approach using a laryngeal endoscope, even though the hFVP was 12 cm in length.

Airway management is critical. Tracheotomy or endotracheal intubation allows for controlled ventilation until the polyp can be completely excised. In our review, tracheotomies were performed in 3 patients to protect the airway (Owens et al. 1994; Nuyens et al. 2004; Ozdemir et al. 2011). These three cases had the following features: multiple synchronous FVPs, a long body, and a wide and thick pedicle that might cause laryngeal blockage. In the present case, in spite of double pedicle polyps and a relatively long body, the narrow airway due to the tumor could be secured by orotracheal intubation, and thus tracheotomy could be avoided. When patients experience respiratory distress with regurgitation of the tumor after vomiting, we have to consider FVP. When there is high risk of aspiration or surgical resection cannot be performed rapidly, the airway should be secured by preoperative intubation or tracheotomy.

Conclusions

We encountered an extremely rare case of a vast hFVP that caused dyspnea, and we also reviewed 13 cases of hFVP. Giant hFVPs are life-threatening because of potential complete airway obstruction and sudden asphyxia due to laryngeal blockage. Thus, when such cases are encountered, airway management and surgical treatment should be considered as early as possible.

Abbreviations

FVP: 

fibrovascular polyp

hFVP: 

hypopharyngeal fibrovascular polyp

CT: 

computed tomography

MRI: 

magnetic resonance imaging

Declarations

Authors’ contributions

All authors were co-attending otolaryngologist for this patient. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Written informed consent was obtained from the patient for publication of this Case Report.

Ethics approval and consent to participate

This study was approved by the Human Ethics Committee of the University of Tokyo (No. 2487) and the Ethics Review Board of the Tokyo Postal Services Agency Hospital and informed consent was obtained from the patient in this study.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors’ Affiliations

(1)
Department of Otolaryngology Head and Neck Surgery, Tokyo Metropolitan Tama Medical Center
(2)
Department of Otolaryngology, The University of Tokyo

References

  1. Al-Swiahb JN, Al-Dousary SH (2008) Fibrovascular polyp of the hypopharynx. Ann Saudi Med 28(3):217–219View ArticleGoogle Scholar
  2. Avezzano EA, Fleischer DE, Merida MA, Anderson DL (1990) Giant fibrovascular polyps of the esophagus. Am J Gastroenterol 85(3):299–302Google Scholar
  3. Caceres M, Steeb G, Wilks SM, Garrett HE Jr (2006) Large pedunculated polyps originating in the esophagus and hypopharynx. Ann Thorac Surg 81(1):93–96View ArticleGoogle Scholar
  4. Gupta M, Chaudhary N, Gupta M (2011) Fibrovascular polyp of the oropharynx. Singapore Med J 52(2):e35–e36Google Scholar
  5. Haytoglu S, Tuhanioglu B, Bozkurttan A, Arikan OK (2015) Giant hypopharyngeal fibrovascular polyp: a case report and review of the relevant literature. Case Rep Otolaryngol. doi:10.1155/2015/670302 Google Scholar
  6. Kim JS, Shim YM (2006) Giant fibrovascular polyp of the hypopharynx: surgical treatment with the biappoach. J Korean Med Sci 21:749–751View ArticleGoogle Scholar
  7. Lee SY, Chan WH, Sivanandan R, Lim DTH, Wong WK (2009) Recurrent giant fibrovascular polyp of the esophagus. World J Gastroenterol 15(29):3697–3700View ArticleGoogle Scholar
  8. Lee EJ, Hong SG, Baek HR et al (2013) A case of large fibrovascular polyp of the stomach. Clin Endosc 46:186–188View ArticleGoogle Scholar
  9. Nascimento SB, Santos FC, Pinheiro MNSM (2014) Giant fibrovascular polyp of the Larynx. Int Arch Otorhinolaryngol 18:325–327View ArticleGoogle Scholar
  10. Nuyens MR, Bhatti NI, Flint P (2004) Multiple synchronous fibrovascular polyps of the hypopharynx. ORL J Otorhinolaryngol Relat Spec 66(6):341–344View ArticleGoogle Scholar
  11. Owens JJ, Donovan DT, Alford EL et al (1994) Life-threatening presentations of fibrovascular esophageal and hypopharyngeal polyps. Ann Otol Rhinol Laryngol 103:838–842View ArticleGoogle Scholar
  12. Ozdemir S, Gorgulu O, Selcuk T, Akbas Y, Sayar C, Sayar H (2011) Giant fibrovascular polyp of the hypopharynx: per-oral endoscopic removal. J Laryngol Otol 125(10):1087–1090View ArticleGoogle Scholar
  13. Paik HC, Han JW, Jung EK, Bae KM, Lee YH (2001) Fibrovascular polyp of the esophagus in infant. Yonsei Med J 42:264–266View ArticleGoogle Scholar
  14. Pallabazzer G, Santi S, Biagio S, D’Imporzano S (2013) Difficult polypectomy-giant hypopharyngeal polyp: case report and literature review. World J Gastroenterol 19(35):5936–5939View ArticleGoogle Scholar
  15. Sargent RL, Hood IC (2006) Asphyxiation caused by giant fibrovascular polyps of the esophagus. Arch Pathol Lab Med 130:725–727Google Scholar
  16. Timmons B, Sedwitz JL, Oller DW (1991) Benign fibrovascular polyp of the esophagus. South Med J 84:1370–1372View ArticleGoogle Scholar
  17. Wang J, Han DM, Ni X, Ma LJ, Ye JY, Xiao Y (2011) Fibrovascular polyp of the hypopharynx and esophagus. Chin Med J (Engl) 124(19):3182–3184Google Scholar
  18. Zevallos JP, Shah RP, Baredes S (2005) Giant fibrovascular polyp of the hypopharynx. Laryngoscope 115(5):876–878View ArticleGoogle Scholar

Copyright

© The Author(s) 2016