Hairy Polyp Research Articles

Hairy Polyp Presenting With Respiratory Distress in an Infant With Cleft Palate

Hairy Polyp Presenting With Respiratory Distress in an Infant With Cleft Palate

A Case of a Eustachian Tube Hairy Polyp Misdiagnosed as an Adenoid Residual in a Child.

Hairy polyps, considered a highly unusual congenital anomaly of the pharynx, are believed by many scholars to arise from the ectoderm and mesoderm during the embryonic stage. These growths often have a pear or sausage shape, are pedunculated, and their size ranges between 0.5 and 6 cm. They are typically grayish white or pink in color. This article discusses a 12-year-old female who had a growth at the Eustachian tube's entrance on the left side of the nasopharyngeal wall, as identified by a computed tomography scan of the neck soft tissue; it was suspected to be a hairy polyp originating from the left Eustachian tube. The diagnosis of a hairy polyp was confirmed through pathology. The hairy polyp at the Eustachian tube, in this case, showed an irregular form with a wide base, making it look similar to an adenoid; thus, increasing the risk of it being misdiagnosed as residual adenoid tissue.

Bacterial Ball in Concha Bullosa: Report of a Case With Unusual Location

Choristoma, also known as a hairy polyp, is a rare benign mass that commonly occurs in the nasopharynx and oropharynx in the head and neck region. It is usually diagnosed in children and has rarely been reported in adults. In this study, we describe a nasopharyngeal choristoma in an adult man. The mass was located at the lateral nasopharyngeal wall, and the patient expressed intermittent nasal stuffiness and ear fullness. The mass was successfully removed using an endoscopic approach. Since nasopharyngeal choristoma in adults is rare, it is important to distinguish it from other benign tumors located in the nasopharynx or nasal cavity. In this report, we describe the radiologic characteristics of nasopharyngeal choristoma and summarize the importance of differential diagnosis from other benign masses.

CT and MRI Features of Hairy Polyps in Neonates and Infants: A Retrospective Study of 14 Patients.

The typical imaging findings of hairy polyps have been described mostly in case reports. This study was conducted to describe the CT and MRI features of hairy polyps and their common associated abnormalities. Medical records of 14 patients with pathological diagnosis of hairy polyps were collected for this study. For each patient, the medical records, including demographics, clinical manifestations, and imaging findings were reviewed. The female-to-male ratio was 3.7:1. The age at first episode varied from birth to 2.7 years. The masses were derived from the back side of the soft palate in seven (50.0%) cases, from the lateral pharyngeal wall in four (28.6%) cases, from the soft palate in one (7.1%) case, from the nasal vestibule in one (7.1%) case, and from the parapharyngeal space in one (7.1%) case. A total of 11 (78.6%) cases presented with pedicled masses containing fat and a central core of soft tissue, there were 3 (21.4%) cases whose imaging findings were atypical, and there were 6 (42.9%) patients who had other pathologies. Hairy polyps typically presented as pedicled masses containing fat and a central core of soft tissue, but sometimes their imaging findings can be atypical and they can be associated with other congenital abnormalities. CT and MRI are reliable methods for the diagnosis of hairy polyps and their associated abnormalities.

CONGENITAL HAIRY POLYP ASSOCIATED WITH TERATOMA IN A NEWBORN WITH HYDROCEPHALUS: A RARE CASE REPORT

Congenital tumors in the oral cavity are rare. Among these, hairy polyps (HP) are benign lesions containing elements of ectodermal and mesodermal origin, whereas oral teratomas (OT) include all 3 germ cell layers. We present a 21-day-old female newborn, diagnosed with hydrocephalus and severe right ventriculomegaly, showing a polyp-like lesion in the oral cavity, associated with feeding and breathing difficulties. Computed tomography confirmed the presence of a large pedunculated mass, measuring 3.6 × 1.5 × 1.1 cm, arising in the soft palate, obstructing the oropharynx. Histopathologic examination showed central mature adipose tissue, hair follicles, sebaceous glands, and neurovascular structures, lined by stratified squamous keratinized epithelium, in the nodule region compatible with HP. We also found the presence of cartilaginous, glandular, lymphatic proliferation, osseous and immature myxoid tissue, confirming an associated OT. The lesion was removed surgically, and the patient remains in intensive care because of systemic complications.

A Rare Adult Case of Choristoma in Nasopharynx Obstructing the Eustachian Tube: Case Report and Review of the Literature

Choristoma, also known as a hairy polyp, is a rare benign mass that commonly occurs in the nasopharynx and oropharynx in the head and neck region. It is usually diagnosed in children and has rarely been reported in adults. In this study, we describe a nasopharyngeal choristoma in an adult man. The mass was located at the lateral nasopharyngeal wall, and the patient expressed intermittent nasal stuffiness and ear fullness. The mass was successfully removed using an endoscopic approach. Since nasopharyngeal choristoma in adults is rare, it is important to distinguish it from other benign tumors located in the nasopharynx or nasal cavity. In this report, we describe the radiologic characteristics of nasopharyngeal choristoma and summarize the importance of differential diagnosis from other benign masses.

Hairy Polyp of the Oropharynx: An Unusual Cause of Choking, Feeding Problems in a Newborn

Hairy polyp is an unusual, rare benign developmental malformation of neonates and infants. Embryologically, they are benign lesions containing of both ectodermal and mesodermal origin. Based on size, location of the lesion, they can produce symptoms such as feeding difficulties, airway obstructions, apneic episodes. We present a case of hairy polyp at Oro/Nasopharynx causing feeding difficulties immediately after birth. We explained the mode of presentation, imaging studies, treatment, and review of literature of congenital hairy polyp/choristoma.

Acute upper airway obstruction by a hairy polyp in an infant

Acute upper airway obstruction by a hairy polyp in an infant

Clinical and imaging features of middle ear hairy polyps

Objective: To collect the clinical cases of middle ear hairy polyp, and to summarize the imaging features. Methods: We retrospectively analyzed the clinical data of four cases middle ear hairy polyp confirmed by surgical and pathologic between January 2007 and January 2020 at the Affiliated Eye & ENT Hospital of Fudan University. There were three females, one male, with two left ears and two right ears, aged from 1 to 59 years. The CT and MRI imaging of the patients, and the corresponding clinical manifestations were analyzed. Results: Hairy polyps originated from tympanum in one case, originated from Eustachian tube in two cases, exhibiting recurrent otorrhea without evident inducement. The other case, hairy polyps originated from the Eustachian tube pharyngeal orifice and protruded into the nasopharyngeal cavity, with pharynx discomfort and aural fullness, endoscope showed offwhite polypoid mass with a little hair. All the four cases presented polypoid soft tissue masses on CT and MRI imaging, containing soft tissue wall and a large amount of adipose tissue, with soft tissue in the center of the mass which liked the core, and enhanced. MRI showed stratified arrangement of fat and soft tissue in the wall of the mass. Four cases all had surgical treatment, postoperative pathology examination presented that hair follicles, mature sebaceous glands and other skin appendages were found under squamous epithelium. A large amount of adipose tissue, part of muscle tissue, cartilage tissue, and some fibro-collagenous tissue were proliferated in the mass, accompanied by collagen degeneration. Conclusion: The middle ear hairy polyps has imaging characteristics, the polypoid soft tissue mass usually looks smooth and contains a large amount of adipose tissue, with a soft tissue in the center, and can be suggestively diagnosed by CT and MRI.

THE “-OMAS” and “-OPIAS”: Targeted and Philosophical Considerations Regarding Hamartomas, Choristomas, Teratomas, Ectopias, and Heterotopias in Pediatric Otorhinolaryngologic Pathology

The spectrum of "developmental" lesions that occur in the head and neck predominantly congenital in origin and arising at birth and/or discovered in childhood is broad and fascinating. These have been grouped into categories such as "ectopias", "heterotopias", "hamartomas", and "choristomas". On a philosophical and consequently systematic level, these lesions, mostly benign tumors seem to lack a true understanding of the pathogenetic foundation on which to base a more unified taxonomic designation. In this review, we will consider some of these select tumors as they represent syndromic associations (nasal chondromesenchymal hamartoma and DICER1 syndrome), the lingual choristoma from the perspective of its nomenclature and classification, lesions with ectopic meningothelial elements, and teratomas and the enigmatic "hairy polyp" in reference to a broader discussion of pathogenesis and pluripotent cells in the head and neck. A consistent thread will be how these lesions are designated with some final thoughts on future directions regarding the investigation of their pathogenesis and taxonomic nomenclature.

Hairy Polyp

(Figure 1) A female infant was delivered at 39 weeks gestation by emergent cesarean section to a 27-year-old G3P1. The patient was initially cyanotic and tachypneic. She was admitted to the NICU for ongoing supplemental oxygen. After gagging during attempted feeding, a relatively large (2.7 x 1.9 x 0.7 cm) lesion was retrieved from the oral cavity (Panel A). It had a very narrow stalk and was covered with numerous fine hairs. Histologically, much of the specimen was composed of fibroadipose tissue with a few hair follicles along the periphery. Hairy polyps are rare naso-oropharyngeal tumors usually associated with respiratory and feeding difficulties shortly after birth. Their etiology and precise classification remains uncertain..

Analysis on clinical characteristics, diagnosis and treatment of 13 cases of infant hairy polyp

Objective: To explore and analyze the clinical characteristics, diagnosis and treatment of infant hairy polyp. Methods: A retrospective analysis was made on 13 cases of hairy polyp confirmed by pathology, who were admitted to the Children's Hospital of Hebei Province from January 2010 to September 2019, including 4 males and 9 females, with a male-female ratio of 1∶2.25. The age ranged from 3 hours to 1 year, and the median age was 1 month. Twelve of the 13 children were found to have difficulty breathing or feeding. All the children received coblation resection under general anesthesia. The root pedicle of the mass was found in the lateral nasopharyngeal wall in 8 cases, in the junction of palatine and palatopharyngeal arch of tonsil and the tongue and esophageal entrance in 1 case, respectively. Nasal septum was found in 2 cases, including 1 case located between two incisors. The wound at the root pedicle was ablated and the bleeding was stopped completely. Results: Postoperative follow-up lasted from 3 months to 2 years, and there was no recurrence in 12 cases. Fibrolaryngoscope showed a mass of the right eustachian tube and pharyngeal mouth in 1 case 2 years after the surgery, which was considered recurrence of hairy polyps and lost after that. Conclusion: Hairy polyps in infants is a rare clinical disease, and its main symptom is upper respiratory tract obstruction. Early diagnosis and radical surgery are the key to the treatment of the disease.

Hairy Polyp Arising From the Nasal Vestibule.

Hairy Polyp Arising From the Nasal Vestibule.

Hairy Polyp of the Nasopharynx Associated With Hypoplastic Soft Palate, Low Eustachian Tube Orifice, and Tonsil

Hairy Polyp of the Nasopharynx Associated With Hypoplastic Soft Palate, Low Eustachian Tube Orifice, and Tonsil

Oropharyngeal Hairy Polyp: A Case of Respiratory Failure in a Newborn

Hairy polyps, also known as dermoid polyps (DPs), are rare benign cystic lesions of bigerminal origin that may occur in several head and neck regions, including the oropharynx. Despite their benign histopathological nature, DPs may be life threatening, due to their upper airway location, and DPs represent one of the most unusual causes of respiratory distress during the neonatal period. In this paper, we describe a case of respiratory failure in a newborn with an oropharyngeal mass that was accidentally found during difficult intubation. Magnetic resonance imaging (MRI) detected a well-defined soft tissue pedunculated mass, arising from the left oropharynx wall, consistent with an oropharyngeal DP. The newborn had a prompt recovery after trans-oral mass removal. Our case underlines the importance of imaging in differential diagnosis of children’s respiratory distress, secondary to a variety of lesions within the region of the skull base or oropharynx. It allowed us to assess the origin of the lesion, as well as its relationship with the adjacent soft tissues, and to exclude intracranial extension, thus providing essential information for the surgical planning.

Hairy polyp of the rhinopharynx – a rare and unrecognized entity

Hairy polyp of the rhinopharynx – a rare and unrecognized entity

Imaging features of pharyngeal hairy polyps in infants.

Hairy polyps are the most common congenital deformity of the oral-nasopharynx/oral cavity in infants, which may lead to severe complications in the newborns. However, few studies have been published with respect to their radiological features, and most are case reports. This study aimed to analyze radiological features of the oral‑nasopharyngeal hairy polyps and to identify the radiological features with the highest diagnostic value. From 2014 to 2019, pediatric cases pathologically diagnosed as hairy polyps and having received radiological examination at the Children's Hospital Affiliated to Zhejiang University were retrospectively analyzed. Radiological evaluations were conducted on tumor size, location, morphology, density or signal features as well as the enhancement pattern. A total of six infants were recruited. Clinical features observed in these cases included choking on milk with cyanosis, intermittent dyspnea, oropharyngeal mass, and snoring. Lesions were derived from the left tubal torus in three out of six cases, from the left lateral aspect of soft palate in one, from the left lateral pharyngeal wall in one, and from the right tubal torus in one. They were shown as pedicled polyp-like well-circumscribed mass with fat density or signal as well as a stalk on CT or MRI. In the contrast-enhanced scan, the fat components were not enhanced, while the stalk was mildly enhanced. Hairy polyps had typical radiological features. Hairy polyps should be considered for pedicled polyp-like well-circumscribed mass in the oral-nasopharynx of infants with fat density or signal as well as a stalk.

Hairy Polyp in the Nasopharynx - A Case Report

Background: Hairy polyp or dermoid is a benign bigerminal congenital germ cell tumour. It is a rare condition in the nasopharynx. Hairy polyp in head and neck region consists less than 5% of that occurs in whole body.
 Objective: To report a rare nasopharyngeal benign condition presented without obstructive symptoms.
 Case: A four-year-old female child presented with a pedunculated dermoid tumour attached to the left lateral wall of nasopharynx. There was an associated unilateral cleft in soft palate. The tumour was removed by dissecting with bipolar diathermy by combined endonasal endoscopic and transoral approach.
 Conclusion: Hairy polyp in nasopharynx may present as an incidental asymptomatic mass in throat and may be associated with a cleft palate.
 Bangladesh J Otorhinolaryngol; April 2017; 23(1): 92-95

Pharyngeal hairy polyps: Case series and literature review.

It was aimed to report 5 cases of pharyngeal hairy polyps, and to summarize the characteristics combined with literature review.Five cases with pathological diagnosis of pharyngeal hair polyps were diagnosed and treated in our department from June, 2006 to October, 2016, and retrospective analysis of their clinical data was performed. Among the 5 cases, there were 1 male and 4 female, with the age of 2 days to 26 months old. After birth, these patients were accompanied by stridor, difficulty breathing, snoring, feeding difficulties, and slow weight gain.Gray mass in the stem original from the pharynx was found in all 5 cases, with the surface hair-covering. The polyp resections were performed under general anesthesia, with the complete removal of polyp along the pars basilaris during surgery smoothly. The operation during was 5 to 20 minute, with an average of 12 minute, and there was little hemorrhage during operation. Symptoms disappeared completely after the surgery, and follow-up was performed for 1 year without recurrence shown.Pharyngeal hairy polyp is a rare non-malignant clinical disease, mainly caused by symptoms in respiratory tract obstruction. Complete removal of polyps along the pars basilaris is an effective treatment, with no recurrence case reported after surgery.

Congenital hairy polyp - a case report

Introduction. Hairy polyp is a rare malformation which consists of mesodermal and ectodermal elements. It is the most common congenital nasopharyngeal tumour. The clinical symptoms depend on the size and localization of the mass. Early surgical excision results in permanent cure. Case report. The child was born from regularly controlled pregnancy. Prenatally, in the 24th week of gestation, epulis gigantocellularis was suspected, magnetic resonance imaging confirmed existence of protruding mass. Immediately after the birth, a tissue formation connected with the hard palate was observed protruding out of the mouth, as well as split of soft palate and tongue. In the first day of life the child was intubated and a mechanical ventilatory support started. In the fourth day of life, tracheostomy was performed. In the 40th day of life, the tumor mass was entirely excised with the reconstruction of the existing deformity of the mouth. The histopathological analysis confirmed the diagnosis of hairy polyp. In the fifth month of life, a percutaneous endoscopic gastrostomy was placed. At the beginning of the second age, the split of tongue and soft palate was sewn. With the establishment of normal swallowing, decannulation and closing of tracheostomy were performed and then gastrostomy was closed. Conclusion. Although the hairy polyp is a rare tumor, it must be included in the differential diagnosis of pharyngeal mass in the neonatal period. If there are no associated anomalies and if complete surgical resection of the tumor is performed, further course of the treatment will be favourable.