RESUMEN
PURPOSE: ChatGPT (Chat-Generative Pre-trained Transformer) has proven to be a powerful information tool on various topics, including healthcare. This system is based on information obtained on the Internet, but this information is not always reliable. Currently, few studies analyze the validity of these responses in rhinology. Our work aims to assess the quality and reliability of the information provided by AI regarding the main rhinological pathologies. METHODS: We asked to the default ChatGPT version (GPT-3.5) 65 questions about the most prevalent pathologies in rhinology. The focus was learning about the causes, risk factors, treatments, prognosis, and outcomes. We use the Discern questionnaire and a hexagonal radar schema to evaluate the quality of the information. We use Fleiss's kappa statistical analysis to determine the consistency of agreement between different observers. RESULTS: The overall evaluation of the Discern questionnaire resulted in a score of 4.05 (± 0.6). The results in the Reliability section are worse, with an average score of 3.18. (± 1.77). This score is affected by the responses to questions about the source of the information provided. The average score for the Quality section was 3.59 (± 1.18). Fleiss's Kappa shows substantial agreement, with a K of 0.69 (p < 0.001). CONCLUSION: The ChatGPT answers are accurate and reliable. It generates a simple and understandable description of the pathology for the patient's benefit. Our team considers that ChatGPT could be a useful tool to provide information under prior supervision by a health professional.
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Otolaringología , Humanos , Encuestas y Cuestionarios , Reproducibilidad de los Resultados , Internet , Enfermedades Nasales/diagnósticoRESUMEN
We present a case of nasopalatine duct cyst in a 35-yearold female. The cyst was diagnosed based on the presence of only one clinical symptom and no obvious clinical signs, which is a relatively rare occurrence. However, the radiographic and histological presentation of this lesion was typical of a nasopalatine duct cyst. Therefore, this case report aims to highlight the variable presentations of the nasopalatine cyst, which is often misdiagnosed and treated as an endodontic infection.
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Quistes no Odontogénicos , Humanos , Femenino , Adulto , Quistes no Odontogénicos/diagnóstico , Quistes no Odontogénicos/diagnóstico por imagen , Quistes no Odontogénicos/cirugía , Quistes no Odontogénicos/patología , Diagnóstico Diferencial , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/diagnóstico por imagen , Enfermedades Nasales/patología , Quistes/diagnóstico por imagen , Quistes/diagnóstico , Paladar Duro/diagnóstico por imagen , Paladar Duro/patologíaRESUMEN
BACKGROUND: Bifid nose is a rare congenital deformity and the etiology is unknown. The purpose of this study was to report genetic variation in family of patients with bifid nose. METHODS: Twenty-three consecutive patients who were diagnosed with mild bifid nose were operated with z-plasty from 2009 to 2021. Three underage patients (a pair of twins and a girl) from two family lines, who came to our hospital for surgical treatment, were enrolled. Whole exome sequencing and Sanger sequencing were conducted. Z-shaped flaps were created and the cartilago alaris major were re-stitched. Photographs and CT scan before and after surgery were obtained. Clinical outcomes, complications and patients' satisfaction were evaluated and analyzed. The follow-up time ranges from 2 to 3 years (2.4 ± 1.2 years). RESULTS: Most patients were satisfied with the outcome (96.2%). The nasal deformities were corrected successfully with z-plasty technique in one-stage. FREM1 c.870_876del and c.2 T > C were detected with Whole exome sequencing, which have not been reported before. The results of Sanger sequencing were consistent with those of Whole exome sequencing. CONCLUSIONS: The newly detected mutations of FREM1 have a certain heritability, and are helpful to make an accurate diagnosis and provide a better understanding of bifid nose mechanism. Z-plasty technique can be an effective technical approach for correcting mild bifid nose deformity.
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Enfermedades Nasales , Nariz , Femenino , Humanos , Mutación , Nariz/anomalías , Nariz/cirugía , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/cirugía , Tomografía Computarizada por Rayos XRESUMEN
Objective: To explore the clinical characteristics, pathological features, and diagnosis and treatment strategies of nasal chondromesenchymal hamartoma (NCMH) in infants and young children. Methods: A retrospective analysis was conducted on seven cases of NCMH infants and young children admitted to Beijing Children's Hospital, Capital Medical University from April 2015 to January 2022. The cohort included 5 males and 2 females, aged from 6 days to 2 years and 3 months. General information, clinical symptoms, imaging findings, treatment plans, postoperative complications, recurrence and follow-up time were collected, summarized and analyzed. Additionally, immunohistochemical characteristics of the lesion were examined. Results: The clinical symptoms of 7 children included nasal congestion, runny nose, open mouth breathing, snoring during sleep, difficulty feeding, and strabismus. All patients underwent electronic nasopharyngoscopy examination, with 5 cases of tumors located in the right nasal cavity and 2 cases in the left nasal cavity. No case of bilateral nasal cavity disease was found. All 7 patients underwent complete imaging examinations, with 5 patients underwent MRI and CT examinations, 1 patient underwent CT examination only, and 1 patient underwent MRI examination only. The CT results showed that all tumors were broad-based, with uneven density, multiple calcifications and bone remodeling, and some exhibited multiple cystic components. The MRI results showed that the tumor showed low signal on T1 weighted imaging and high or slightly high signal on T2 weighted imaging. All patients were diagnosed through histopathological examination and immunohistochemistry, including 7 cases of Ki-67 and SMA (+), 5 cases of S-100 and Vimentin (+), and all EMA and GFAP were negative. All patients underwent endoscopic resection surgery through the nasal approach, with 3 cases using navigation technology. Five cases of tumors were completely removed, and two cases of tumors were mostly removed. No nasal packing was performed after surgery, and no postoperative nasal, ocular, or intracranial complication occurred in all patients. Follow up assessments conducted 6 to 84 months post-surgery revealed no instances of tumor recurrence in any of the patients. Conclusions: The clinical symptoms of children with NCHM mainly depend on the size and location of the tumor. Nasal endoscopic surgery is the main treatment method. In cases where critical structures like the skull base or orbit are implicated, staged surgical interventions may be warranted. Long-term follow-up is strongly advised to monitor for any potential recurrence or complications.
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Hamartoma , Enfermedades Nasales , Masculino , Lactante , Niño , Femenino , Humanos , Preescolar , Cartílagos Nasales/patología , Estudios Retrospectivos , Recurrencia Local de Neoplasia , Enfermedades Nasales/diagnóstico , Hamartoma/diagnóstico , Hamartoma/cirugía , Hamartoma/patologíaRESUMEN
Despite the widespread adoption of nasal endoscopy (NE) in the evaluation of sinonasal disease, its diagnostic potential may still be underutilized. Developments in endoscopic technology have led to significant improvements in video quality and maneuverability. However, there is concern that NE continues to be used primarily for the identification of gross pathology, with relative neglect of more subtle findings such as surface features of inflammation and mucus. With fewer technical limitations to perceive these abnormalities, there is potential to greatly improve the diagnostic value of NE. The reader is herein asked to consider several important visual nuances encountered during NE, with the hope that this engenders an appreciation of the versatility of NE as a diagnostic tool.
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Endoscopía , Humanos , Endoscopía/métodos , Senos Paranasales/diagnóstico por imagen , Enfermedades de los Senos Paranasales/diagnóstico , Nariz/patología , Enfermedades Nasales/diagnósticoRESUMEN
Nasal chondromesenchymal hamartoma (NCMH) is a rare benign polypoid mesenchymal tumor arising in the nasal cavity and/or paranasal sinuses. Recognizing these sporadic, rare lesions is crucial, as surgical complete removal of the mass is the common treatment approach. This retrospective study analyzed the demographics, symptoms, and imaging data of 9 patients diagnosed with NCMH between January 2017 and June 2023, possibly representing the largest single-center adult case cohort to date. Diagnostic techniques included nasal endoscopy, CT/MRI scan, immunohistological studies, and morphologic comparisons. Pathologic specimens were subjected to Sanger sequencing of exons 24 and 25 of DICER1. The average age of 9 cases was 24.4 years, and the oldest was 55 years. Four of the patients were children, ranging from 1 year old to 11 years old, with an average of 4.5 years. Nasal congestion is the most common registered symptom. Endoscopic findings showed that most patients had smooth pink neoplasms or polypoid masses in the nasal meatus. Radiologic scanning revealed soft-tissue density masses that occupied the nasal cavity. Histologically, the characteristic structure of NCMHs is immature cellular cartilage nodules and mature cartilage nodules distributed in a loose mucoid matrix. Five of the 9 patients had somatic DICER1 missense mutations. Four of the patients with DICER1-mutated NCMH exhibited a p.E1813 missense hotspot mutation. We also report a case of a rare p.P1836H missense mutation. The detected DICER1 somatic mutations provide compelling evidence of an association with the DICER1 tumor family. We emphasize the importance of pathologic consultation and the need for pathologists to accumulate experience in NCMH diagnosis to avoid misdiagnosis.
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Hamartoma , Neoplasias de los Tejidos Conjuntivo y Blando , Enfermedades Nasales , Niño , Lactante , Adulto , Humanos , Adulto Joven , Estudios Retrospectivos , Enfermedades Nasales/genética , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/patología , Cavidad Nasal/patología , Hamartoma/genética , Hamartoma/patología , Ribonucleasa III/genética , Neoplasias de los Tejidos Conjuntivo y Blando/patología , Mutación , ARN Helicasas DEAD-box/genéticaRESUMEN
OBJECTIVES: The role of bacterial communities in the pathophysiology of canine nasal disease is still unclear. How and when to treat dogs with suspected secondary bacterial rhinitis and on which test to rely before making a decision to treat with antimicrobials has not been established. The objective is to compare the results of bacterial identification using agar-plate cultures and 16S rRNA gene amplicon sequencing in dogs with nasal discharge suspected to be of bacterial origin. MATERIALS AND METHODS: Twenty-nine client-owned dogs presented for investigation of nasal disease were included in the study. Paired swabs were collected from the same affected nasal cavity. One swab was streaked on 4 agar media (Columbia Blood Agar, MacConkey, Chapman and Edward's). The other swab was stored in a sterile cryotube at -80°. Extracted DNA underwent a polymerase chain reaction targeting the V1-V3 region of the 16S rRNA gene. RESULTS: At least one of the species detected by amplicon sequencing with a relative abundance of >10% was also identified by culture in 14 cases (48.3%), in association with marked predominance of one taxon (>80% relative abundance) in six of 14 cases. In 12 dogs (41.4%), the cultured isolates were rare or undetected components of the corresponding sequence libraries. A negative culture in the face of bacterial predominance (>50% relative abundance) of a potentially pathogenic bacteria detected by sequencing occurred in 17% (n=5) of cases; however, the use of other agar media may have decreased this percentage. CLINICAL SIGNIFICANCE: Standard culture does not reliably predict the bacterial profile detected by 16S rRNA gene amplicon sequencing.
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Enfermedades de los Perros , ARN Ribosómico 16S , Animales , Perros , Enfermedades de los Perros/microbiología , Enfermedades de los Perros/diagnóstico , ARN Ribosómico 16S/genética , ARN Ribosómico 16S/análisis , Masculino , Femenino , Bacterias/aislamiento & purificación , Bacterias/genética , Bacterias/clasificación , Reacción en Cadena de la Polimerasa/veterinaria , ADN Bacteriano/análisis , Enfermedades Nasales/veterinaria , Enfermedades Nasales/microbiología , Enfermedades Nasales/diagnósticoRESUMEN
OBJECTIVES: Empty nose syndrome (ENS) is an underdiagnosed but burdensome clinical condition. Studies that have addressed the impact of remnant inferior turbinate volume (ITV) on ENS are scarce. We aimed to evaluate the impact of ITV and phenotyping on the severity and presentation of ENS. METHODS: All the enrolled patients underwent the following subjective assessments: the ENS 6-Item Questionnaire (ENS6Q), Sino-Nasal Outcome Test-25 (SNOT-25), Beck Depression Inventory-II (BDI-II) and Beck Anxiety Inventory (BAI). The ITV was obtained from finely cut (1-mm-thick slices) sino-nasal computed tomography scan images and analyzed using ImageJ. The correlation between ITV, subjective measurements, and morphology of inferior turbinates was evaluated. ENS was categorized as torpedo type (balanced tissue volume) or pistol type (posterior dominance) based on the morphology. RESULTS: Overall, 54 patients met the inclusion criteria. The ITV was positively correlated with the ENS6Q score and domain of ENS symptoms in SNOT-25. Neither BDI-II nor BAI scores had a significant correlation with ITV. Based on their morphological classification, the torpedo type exhibited diverse manifestations in the SNOT-25 analysis in response to changes in ITV, while the pistol type demonstrated an elevated rhinologic symptom burden and ENS-specific symptoms as their ITV increased. Nasal resistance did not correlate with the ITV in either type of ENS. CONCLUSIONS: Symptoms were paradoxically worse in ENS patients with greater remnant ITV, and distinct morphological phenotypes in the nasal cavities may result in different presentations. Further investigation into the correlation between remnant inferior turbinates and nerve function is warranted. LEVEL OF EVIDENCE: 3 Laryngoscope, 134:3060-3066, 2024.
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Obstrucción Nasal , Tomografía Computarizada por Rayos X , Cornetes Nasales , Humanos , Cornetes Nasales/diagnóstico por imagen , Cornetes Nasales/patología , Femenino , Masculino , Adulto , Persona de Mediana Edad , Síndrome , Obstrucción Nasal/diagnóstico por imagen , Obstrucción Nasal/diagnóstico , Encuestas y Cuestionarios , Prueba de Resultado Sino-Nasal , Enfermedades Nasales/patología , Enfermedades Nasales/diagnóstico por imagen , Enfermedades Nasales/diagnóstico , Índice de Severidad de la Enfermedad , Anciano , FenotipoRESUMEN
BACKGROUND: Rhino-orbital-cerebral mucormycosis (ROCM) is a rare, opportunistic, angio-invasive, and fatal infection caused by mold fungi of the genera Rhizopus, Mucor, and Rhizomucor. The global incidence of ROCM is 0.005-1.7 per million, with a fatality rate of 46%. Early diagnosis and treatment are crucial for this disease, as a delay of one week can increase the mortality rate to 66%. CASE: A 32-year-old male, a known case of coronavirus disease 2019 (COVID-19) for the past 15 days from Janakpur, Dhanusha, Nepal presented to the emergency department of Dhulikhel Hospital with a sudden onset of blurred vision in the left eye, left-sided ocular pain, and nasal bleeding for the last three days. OBSERVATIONS: The patient was suspected of post-COVID-19 mucormycosis, and a nasal swab for potassium hydroxide (KOH) mount showed hyphae in microscopy. Intravenous and retrobulbar liposomal amphotericin B were administered as medical therapy, along with surgical debridement. A multidisciplinary approach was necessary for the treatment. CONCLUSION: A long-term, multimodal treatment approach involving combined antifungal drug therapy (intravenous liposomal amphotericin B and retrobulbar amphotericin B), and timely surgical debridement leads to an improvement in both short-term and long-term outcomes.
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Antifúngicos , COVID-19 , Infecciones Fúngicas del Ojo , Mucormicosis , Enfermedades Orbitales , SARS-CoV-2 , Humanos , Mucormicosis/diagnóstico , Mucormicosis/terapia , Masculino , COVID-19/complicaciones , COVID-19/diagnóstico , Adulto , Infecciones Fúngicas del Ojo/diagnóstico , Infecciones Fúngicas del Ojo/microbiología , Infecciones Fúngicas del Ojo/terapia , Infecciones Fúngicas del Ojo/tratamiento farmacológico , Antifúngicos/uso terapéutico , Enfermedades Orbitales/diagnóstico , Enfermedades Orbitales/microbiología , Enfermedades Orbitales/terapia , Anfotericina B/uso terapéutico , Nepal , Enfermedades Nasales/microbiología , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/terapiaRESUMEN
This case report discusses a diagnosis of rhino-orbital-cerebral mucormycosis in a man aged 61 years who presented with vision loss, ophthalmoplegia, and ptosis.
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Infecciones Fúngicas del Ojo , Mucormicosis , Enfermedades Orbitales , Humanos , Mucormicosis/diagnóstico , Mucormicosis/microbiología , Mucormicosis/tratamiento farmacológico , Enfermedades Orbitales/microbiología , Enfermedades Orbitales/diagnóstico , Enfermedades Orbitales/tratamiento farmacológico , Infecciones Fúngicas del Ojo/microbiología , Infecciones Fúngicas del Ojo/diagnóstico , Infecciones Fúngicas del Ojo/tratamiento farmacológico , Masculino , Antifúngicos/uso terapéutico , Imagen por Resonancia Magnética , Enfermedades de los Senos Paranasales/microbiología , Enfermedades de los Senos Paranasales/diagnóstico , Enfermedades de los Senos Paranasales/tratamiento farmacológico , Tomografía Computarizada por Rayos X , Enfermedades Nasales/microbiología , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/tratamiento farmacológico , Femenino , Persona de Mediana Edad , Anfotericina B/uso terapéuticoRESUMEN
Vasculitic midline destructive lesions can be a complication of cocaine use. We report a 44-year-old man who presented with a two months history of left facial pain associated with ipsilateral facial paralysis and a cheek phlegmon. Magnetic resonance imaging showed broad soft tissue destruction linked to important cranial nerve involvement. Antibiotic and antifungal therapy was started and multiple surgical debridement procedures were performed, with no clinical improvement. Microbiological analysis was negative. Finally, thanks to the histologic findings corresponding to vasculitis and granuloma formation and the history of cocaine abuse, a cocaine induced midline destructive lesion was diagnosed.
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Humanos , Masculino , Adulto , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/inducido químicamente , Trastornos Relacionados con Cocaína/complicaciones , Tabique Nasal/efectos de los fármacos , Imagen por Resonancia Magnética , Tomógrafos Computarizados por Rayos X , Granulomatosis con Poliangitis/diagnóstico , Enfermedades Nasales/terapia , Diagnóstico Diferencial , Antibacterianos/clasificación , Antibacterianos/uso terapéuticoRESUMEN
The nasopalatine duct cyst (NPDC) is the most common non-odontogenic cyst typically found in middle-aged Caucasian female in Brazil, however the present report describes a case in a 35 year-old black male. NPDC are usually asymptomatic and are discovered incidentally during routine radiological examination. A cone-beam computed tomography (CBCT) is a valuable tool to localize a cyst within the nasopalatine canal. CBCT enables analysis of the dimension of the NPDC, analysis of the involvement of neighboring anatomical structures and assists in treatment planning. The authors at this case highlight the importance of clinical examination with an unbiased view of age, gender and ethnicity.
O cisto do ducto nasopalatino (CDNP) é o mais comum dos cistos não-odontogênicos geralmente encontrado em mulheres brancas de meia idade no Brasil, embora o presente relato descreva um caso em um homem negro de 35 anos de idade. Os CDNP são usualmente assintomáticos e são descobertos acidentalmente durante o exame radiográfico de rotina. A tomografia computadorizada por feixe cônico(TCFC) é uma ferramenta válida para localizar o cisto dentro do canal nasopalatino. A TCFC permite análise da dimensão do CDNP, análise do envolvimento das estruturas anatômicas vizinhas e auxilia no planejamento do tratamento. Os autores neste caso alertam para a importância do exame clinico, com uma visão embasada na idade, gênero e grupo étnico.
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Humanos , Masculino , Femenino , Adulto , Quistes no Odontogénicos/diagnóstico , Quistes no Odontogénicos/etnología , Quistes no Odontogénicos/prevención & control , Quistes/diagnóstico , Quistes/etnología , Quistes/patología , Quistes/prevención & control , Quistes , Quistes/terapia , Enfermedades Nasales/cirugía , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/etnología , Enfermedades Nasales/patologíaRESUMEN
La incidencia de enfermedades sistémicas que afectan la vía aérea parece ir en aumento, actualmente el diagnóstico cada vez se hace más temprano y fácil gracias al advenimiento del endoscopio, técnicas avanzadas de imagen y laboratorio. Este trabajo busca realizar una revisión general y esquematizada para el abordaje y diagnóstico diferencial de lesiones nasales en enfermedades sistémicas las cuales comparten su forma de presentación clínica.
The incidence of systemic diseases affecting the airway appears to be increasing. Currently the diagnosis is made earlier and more easily thanks to the advent of endoscopes, advanced imaging and laboratory tests. This paper aims to do a general and schematic review to approach and make differential diagnosis of nasal lesions in systemic diseases that share its clinical presentation.
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Enfermedades Nasales/cirugía , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/rehabilitación , Enfermedades Nasales/terapiaRESUMEN
Transsphenoidal surgery is the most commonly used surgical procedure to handle the hypophyseal region, sometimes associated with oronasal complications. MATERIAL AND METHODS/AIM: To evaluate prospectively (specific questionnaire, clinical evaluation) undiagnosed chronic oronasal complications in patients submitted to conventional transsphenoidal adenomectomy surgery, operated at different neurosurgery services more than 6 months ago. RESULTS: 49 patients were evaluated, 37/45 presented macroadenoma. 28,5 percent were submitted to more than one intervention, 2/5 transsphenoidally. Transsphenoidal approach 92.8 percent through sublabial route. No patient had spontaneous complaint. With the specific questionnaire 63.2 percent presented complaints. One patient presented an oronasal fistula, 1 stenosis of the nasal valve area with external nasal deformity. Rhinoscopy detected alterations in 77.5 percent, nasal endoscopy in 87.7 percent. Septal perforation was present in 10/12 patients with scabs and 2 with purulent secretion. All 4 patients submitted to 2 transsphenoidal approaches presented septal perforation and nasal synechiae. In the endonasal, synechiae (2), alteration in medium meatus (1) and stenosis of the nasal valve area (1) were observed. Only two patients presented normal evaluation. CONCLUSION: A high incidence of nasal complications after conventional transsphenoidal surgery observed through examination and not reported spontaneously point to the need of otorhinolaryngological investigation complemented by nasal endoscopy in patients submitted to procedures through this route.
A cirurgia transesfenoidal é o procedimento cirúrgico mais utilizado para abordagem da região hipofisária, sendo por vezes associada a complicações oronasais. MATERIAL E MÉTODOS/OBJETIVO: Estudo prospectivo, através de questionário específico e avaliação clínica complicações oronasais crônicas não-diagnosticadas, em pacientes submetidos à cirurgia transesfenoidal convencional em diferentes serviços de neurocirurgia há mais de 6 meses. RESULTADOS: 49 pacientes, 37/45 com macroadenoma. 14/49 submetidos a mais de uma intervenção, em 2/5 por via transesfenoidal. Abordagem transesfenoidal 92,8 por cento via sublabial. Nenhum apresentava queixa espontânea. Com o questionário específico, 63,2 por cento apresentaram queixas. Um apresentava fístula oronasal, outro, estenose da área de válvula nasal com deformidade nasal externa. A rinoscopia detectou alterações em 77,5 por cento e a endoscopia nasal em 87,7 por cento. Perfuração septal presente em 10/12 pacientes com crostas e 2 com secreção purulenta. Todos 4 pacientes submetidos a 2 abordagens transesfenoidais apresentaram perfuração do septo e sinéquias nasais. Nos casos com abordagem endonasal observaram-se sinéquias2, alteração em meato médio1 e estenose em área de válvula nasal1. Apenas 2 pacientes apresentaram avaliação normal. CONCLUSÃO: Alta incidência de complicações nasais após abordagem transesfenoidal convencional, observadas (exame) e não referidas espontaneamente indicam a necessidad de investigação otorrinolaringológica complementada com endoscopia nasal sistemática nestes pacientes.
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Adulto , Femenino , Humanos , Masculino , Endoscopía/efectos adversos , Hipofisectomía/efectos adversos , Enfermedades Nasales/etiología , Complicaciones Posoperatorias , Neoplasias Hipofisarias/cirugía , Seno Esfenoidal/cirugía , Enfermedad Crónica , Endoscopía/métodos , Hipofisectomía/métodos , Enfermedades Nasales/diagnóstico , Estudios Prospectivos , Encuestas y CuestionariosRESUMEN
Cisto nasolabial é uma lesão rara, localizado próximo à cartilagem alar nasal e que se estende para o meato nasal inferior e sulco gengivo-labial superior. OBJETIVO: Apresentamos uma casuística de cisto nasolabial, com o objetivo de discutir a apresentação clínica, o diagnóstico e as técnicas cirúrgicas mais adequadas no tratamento desta doença. MATERIAL E MÉTODO: Estudo retrospectivo de oito pacientes com diagnóstico de cisto nasolabial, no período de janeiro/2000 a dezembro/2006. O diagnóstico foi sugerido por exame otorrinolaringológico e tomografia computadorizada (TC). Os pacientes foram submetidos a tratamento cirúrgico (enucleação) e o diagnóstico confirmado por exame histopatológico. RESULTADOS: Os sintomas predominantes foram: obstrução nasal, aumento de volume restrito ao vestíbulo nasal e dor à palpação local. O tempo médio de evolução dos sintomas foi de 26,2 meses. A TC evidenciou lesão cística, bem delimitada, com remodelação óssea em alguns casos. O tamanho médio do cisto foi de 2,18 cm. O seguimento médio no pós-operatório foi de 19,5 meses, sem recorrência da lesão. CONCLUSÃO: Os cistos nasolabiais são lesões pouco freqüentes. A maioria apresenta-se com aumento de volume bem localizado, dor local e obstrução nasal. Enucleação é o tratamento de escolha com baixos índices de recorrência.
Nasolabial cyst is a rare lesion situated behind the ala nasi, extending backwards into the inferior nasal meatus and forward into the labio-gingival sulcus. AIM: We present our case of a nasolabial cyst, with the purpose of discussing clinical presentation, diagnosis and the more suitable surgical techniques to treat this disorder. MATERIALS AND METHODS: A retrospective study of eight patients with diagnosis of nasolabial cyst, carried out in the period of january/2000 to december/2006. The diagnosis was suggested by otorhinolaryngology exam and computer tomography. All patients were submitted to surgical treatment (enucleation) and definitive diagnosis was confirmed by histopathology. RESULTS: Predominant symptoms were nasal obstruction, swelling in the nasal vestibule region and local pain. Patients had had symptoms for a median of 26.2 months. CT scan was performed in all patients, showing a well outlined cystic lesion with bone remodeling in some cases. Median sizes of the cysts were 2.18cm. There was no evidence of recurrence during a mean follow-up of 19.5 months. CONCLUSION: Nasolabial cysts are rare lesions. Common presentation is a well-confined swelling, local pain and nasal obstruction. Enucleation is the treatment of choice with low recurrence rate.
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Adulto , Anciano , Femenino , Humanos , Persona de Mediana Edad , Quistes , Enfermedades de los Labios , Enfermedades Nasales , Quistes/diagnóstico , Quistes/cirugía , Estudios de Seguimiento , Enfermedades de los Labios/diagnóstico , Enfermedades de los Labios/cirugía , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/cirugía , Estudios Retrospectivos , Tomografía Computarizada por Rayos XRESUMEN
O cisto nasolabial é um cisto não odontogênico raro que se desenvolve na região inferior da asa nasal, com patogênese ainda incerta. Esta lesão, que possui crescimento lento e dimensões variáveis (1,5-3cm), caracteriza-se clinicamente por uma tumefação flutuante na região do sulco nasolabial ao redor da asa do nariz, causando uma elevação do lábio superior. Seu diagnóstico pode ser feito basicamente pelo quadro clínico e, se necessário, complementando-se com exames auxiliares por imagens. O presente trabalho relata o caso de uma paciente do sexo feminino de 48 anos, que se queixava da presença de uma massa consistente na região da asa esquerda do nariz e cujas características clínicas eram compatíveis com cisto nasolabial. As imagens de TC demonstraram uma formação expansiva com densidade de tecido mole, localizadas na região nasal esquerda medindo cerca de 1,2cm de diâmetro e apresentando contornos nítidos e bem definidos e densidade homogenia ao redor de 50 UH. Já as imagens de RM mostraram uma lesão de aspecto circular localizada em tecido mole, apresentando hiperintensidade nas imagens ponderadas em T1, T2 e no recurso de supressão da gordura, sendo a hipótese diagnóstico de cisto nasolabial, confirmado pelo exame histopatológico depois da cirurgia.
The nasolabial cyst is an uncommon non-odontogenic cyst that develops in the lower region of the nasal ala; its pathogenesis is uncertain. This lesion grows slowly and measures between 1.5 and 3 cm; it is characterized clinically by a floating tumefaction in the nasolabial sulcus, which elevates the upper lip. The diagnosis is based on the clinical findings and, if necessary, image exams. This paper reports a case of a white 48-year-old Brazilian female patient that presented a firm tumor in the left ala of the nose; the clinical features suggested a nasolabial cyst. CT scans revealed an expanding tumor with soft tissue density located in the left ala of the nose. It measured 1.2 cm in diameter and had a clear and well-defined outline; its homogeneous density was about 50 HU. MR images revealed a circular lesion located in soft tissue; T1 and T2 weighted signals were hyperintense, as were images after fat suppression. The diagnosis was a nasolabial cyst, which was confirmed by histopathology after surgery.
Asunto(s)
Femenino , Humanos , Persona de Mediana Edad , Quistes/diagnóstico , Enfermedades de los Labios/diagnóstico , Enfermedades Nasales/diagnóstico , Quistes/cirugía , Enfermedades de los Labios/cirugía , Imagen por Resonancia Magnética , Enfermedades Nasales/cirugía , Tomografía Computarizada por Rayos X , Resultado del TratamientoRESUMEN
O cisto nasolabial caracteriza-se como lesão não-odontogênica de partes moles, rara e com ocorrência em situação paramediana, anteriormente ao rebordo alveolar da maxila e à asa do nariz. Portratar-se de lesão de tecido mole, geralmente não produz alteração radiográfica. No presente trabalho são descritos dois casos de cisto nasolabial, nos quais são evidenciados aspectos relevantes em relação ao diagnóstico diferencial por meio de tomografia computadorizada e ressonância magnética, bem como os aspectos atípicos encontrados em um dos casos relatados, como bilateralidade e diferença de intensidade de sinal à ressonância magnética. São discutidos, ainda, fatores determinantes para o diagnóstico diferencial de lesões de tecido mole do complexo maxilofacial,como cistos fissurais de ocorrência central (sagital), entre eles dermóides, palatinos e nasopalatinos (cisto do canal do incisivo), e cistos de fissura lateral.
The nasolabial cyst is defined as nonodontogenic soft tissue lesion, rare and with occurrence in sagittal plane, between midline and nasal cartilage. Because its soft tissue composition, there is no radiographic presentation in conventional radiographic examination,being indicated evaluation through computed tomography and magnetic resonance imaging. In the present study, two cases are discussed, being one in white female subject, 72-year-old, and other in a black male subject, 24-year-old. The authors discuss about relevant aspects related to differential diagnosis through computed tomography and magnetic resonance imaging, as wellas atypical features founded in one of the cases, like bilateral occurrence with different signal intensity in magnetic resonance imaging and determinant factors for differential diagnosis of softtissues pathologies of maxillofacial complex, as fissure cysts with central occurrence (sagittal cysts), as dermoid cysts, palatine and nasopalatine and lateral fissure cysts.
Asunto(s)
Humanos , Masculino , Femenino , Adulto Joven , Anciano , Quistes/diagnóstico , Enfermedades de los Labios/diagnóstico , Enfermedades Nasales/diagnóstico , Espectroscopía de Resonancia Magnética , Tomografía Computarizada por Rayos X , Diagnóstico DiferencialAsunto(s)
Humanos , Masculino , Persona de Mediana Edad , Histoplasmosis/diagnóstico , Huésped Inmunocomprometido , Enfermedades Nasales/microbiología , Antifúngicos/uso terapéutico , Histoplasmosis/tratamiento farmacológico , Itraconazol/uso terapéutico , Enfermedades Nasales/diagnóstico , Enfermedades Nasales/tratamiento farmacológicoRESUMEN
La displasia osteofibrosa es una patología ósea benigna e idiopática, poco frecuente en cabeza y cuello. Afecta principalmente el hueso maxilar mientras en fosa nasal su frecuencia es baja. Habitualmente aslntomática, puede ser agresiva por crecimiento local y eventual malignización. El tratamiento es quirúrgico cuando produce alteraciones en la estética facial, síntomas compresivos orbitarios, rinosinusales, vasculares, nerviosos o ante sospecha de malignización. Se presenta un caso de un paciente con obstrucción nasal persistente, en cuya evaluación se diagnostica un tumor óseo de cornete inferior, que es extirpado mediante técnica endoscópica, con resultado satisfactorio. El estudio histopatológico confirmó el diagnóstico de displasia osteofibrosa. Se discuten los problemas diagnósticos y terapéuticos, destacando la importancia del examen físico y el diagnóstico oportuno, pudiendo tratarse endoscópicamente sin inconvenientes cuando son pequeños.