ABSTRACT
Los pólipos pilosos nasofaríngeos son tumores benignos poco frecuentes. Se presenta el caso de esta patología en una paciente recién nacida, quien presentó cianosis y dificultad respiratoria por obstrucción de la vía aérea superior, durante las primeras 24 horas de vida. La paciente requirió maniobras de reanimación e intubación endotraqueal. Estudios diagnósticos confirmaron la presencia de una masa en la pared lateral de la faringe. Se realizó la extirpación quirúrgica exitosa con evolución satisfactoria de la paciente
Nasopharyngeal hairy polyps are rare benign tumors. We present a newborn case with a hairy polyp mass causing cyanosis and respiratory distress due to obstruction of the upper airway during the first 24 hours of life. The patient required resuscitation and endotracheal intubation. Diagnostic studies confirmed the presence of a mass in the lateral pharyngeal wall. Surgical treatment and removal of the mass was performed with satisfactory evolution of the patient
Subject(s)
Humans , Female , Infant, Newborn , Nasal Polyps/diagnostic imaging , Resuscitation , Nasal Polyps/surgery , Nasopharyngeal Diseases , Cyanosis , Airway Obstruction , Intubation, Intratracheal , NeoplasmsABSTRACT
O pólipo piloso é um tumor congênito que se manifesta, normalmente, nos primeiros anos de vida, como uma massa coberta com pele contendo glândula sebácea e pelo. Foi descrito, primeiramente, por Brown-Kelly em 1918, com predominância no sexo feminino. A manifestação clínica depende da localização e do tamanho do pólipo, mas, geralmente, causa sintomas respiratórios e alimentares. Há predileção pelo lado esquerdo do organismo, ainda não explicada (1). Não há predisposição genética ou identificação em parentes, e normalmente apresenta-se como um defeito isolado, sem relatos de malignização. O diagnóstico pode ser suspeitado através do estudo de imagem. O tratamento envolve a exérese completa da massa, não havendo necessidade de nenhuma outra complementação (2). Relatamos o caso de uma paciente de 21 anos cujo diagnóstico foi confirmado com anatomopatológico da peça cirúrgica(AU)
The hairy polyp is a congenital tumor that usually manifests in early life as a mass covered with skin containing sebaceous gland and hair. It was first described by Brown-Kelly in 1918, predominantly in females. The clinical manifestation depends on the polyp's location and size, but it usually causes respiratory and feeding symptoms. It is more likely to appear on the left side of the body, a predilection not yet explained. (1) There is no genetic predisposition or identification in relatives, and it usually presents as an isolated defect without malignant reports. The diagnosis may be suspected by imaging. Treatment involves complete excision of the mass, with no need for any other action. (2) We report the case of a 21-year-old patient whose diagnosis was confirmed by pathology of the surgical specimen(AU)
Subject(s)
Humans , Female , Adult , Polyps , Nasopharynx , Surgery, Computer-AssistedABSTRACT
Introduction Dermoids frequently called "hairy polyps" and their nature have not been completely clarified. Objectives To discuss the unusual presentation, symptoms, incidence, histology, and perioperative management of hairy polyps in the light of a case and current literature. Resumed Report A 3-year-old boy presented with intermittent respiratory distress since birth. Oropharyngeal examination revealed a nasopharyngeal mass originating from the supratonsillar fossa. The mass was so mobile that it moved between the oropharynx and the nasopharynx during swallowing. The radiologic and pathologic examinations confirmed the mass as a hairy polyp. Conclusion In a pediatric age group with airway obstruction, hairy polyps of the oropharyngeal region must also be included in the differential diagnosis. .
Subject(s)
Animals , Cnidarian Venoms/chemistry , Lipid Bilayers/chemistry , Lipid Droplets/chemistry , Molecular Imaging/methods , Chickens , Porosity , SheepABSTRACT
Hairy polyps are rare congenital benign masses of the head and neck. They mainly occur in the nasopharynx and oropharynx. This paper reports a 12-month-old female patient who had a 0.5-cm sausage-shaped mass in the left nasal vestibule with nasal obstruction and habitual nose-picking. This lesion was surgically removed with no complications under monitored anesthesia. There was no evidence of recurrence through 24 months. To the best our knowledge, this is the first English literature report of a patient with a hairy polyp arising from a nasal vestibule.
Subject(s)
Female , Humans , Infant , Anesthesia , Head , Nasal Obstruction , Nasopharynx , Neck , Oropharynx , Polyps , RecurrenceABSTRACT
Hairy polyps are rare developmental malformations. They are benign lesions presented as a pedunculated mass that may arise from the naso-oropharyngeal region. Larger mass can cause upper respiratory obstruction causing respiratory distress or feeding diffi culty, while smaller mass will present as intermittent respiratory distress due to a ball-valve type of obstruction. They are commonly seen in female, with ratio of 6:1 and majority of the cases occur in the infantile period. We are reporting a case of hairy polyp in a female infant that causing intermittent respiratory distress.
ABSTRACT
Hairy polyp is an uncommon lesion of the nasopharynx and oropharynx. It is most frequently seen as a pedunculated mass at birth or in the first year of life. It generally has been classified as dermoid derived from the ectoderm and mesoderm. The symptoms depend on the size and location of the lesion. We report the clinico-pathological features of a hairy polyp arising from the right nasopharyngeal side of soft palate in a 21-day-old girl. Grossly, a well demarcated brownish yellow solid mass, measuring 2.7x1.5x1.2 cm, showed fine hairs on the surface. The cut surface was a yellowish brown solid appearance. Microscopically, it was covered with keratinizing squamous epithelium and was composed of mature adipose tissue, skeletal muscle, a few peripheral nerve bundles, and blood vessels in the center and mature pilosebaceous units in the periphery. Knowledge of this type of malformation facilitates early intervention and avoids significant morbidity.