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Gotowe bibliografie tematyczne / Nasal sinus hypoplasia

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Artykuły w czasopismach

Gotowa bibliografia na temat „Nasal sinus hypoplasia”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Nasal sinus hypoplasia"

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Rizvi, Sama, Riya Thakral, Stuti Shukla, and Saurabh Singh. "Intraoperative incidental finding of maxillary hypoplasia: a rare case report." International Journal of Otorhinolaryngology and Head and Neck Surgery 10, no. 1 (2024): 131–33. http://dx.doi.org/10.18203/issn.2454-5929.ijohns20240074.

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Hypoplastic and aplastic paranasal sinuses are rare conditions which can lead to obstruction of mucociliary clearance. most of these patients are asymptomatic, however these conditions may lead to chronic headaches and nasal obstruction which can be misleading towards the diagnosis of chronic rhinosinusitis. it has been reported in literature that conventional radiography could not differentiate between inflammatory pathologies, neoplasm, and hypoplasia of the sinus. Computed tomography and cone beam computed tomography are the modalities of choice to differentiate these conditions, wherein co

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Hanna, Ehab, Howard L. Levine, Sanford Timen, and Bernard Kotton. "Hypoplasia of the Maxillary Antrum: Anatomic Abnormalities, Diagnostic Difficulties and Surgical Implications." American Journal of Rhinology 7, no. 3 (1993): 105–10. http://dx.doi.org/10.2500/105065893781976384.

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Using conventional radiography, maxillary sinus hypoplasia (MSH) may be misdiagnosed as chronic infective sinusitis in patients with chronic nasal symptoms. Commonly associated anatomical abnormalities of the lateral nasal wall and orbit may also be missed. Failure to recognize these abnormalities is fraught with hazards should sinus surgery be contemplated on such patients. With the use of high resolution computed tomography scans and rigid nasal endoscopy, MSH and associated subtle anatomic abnormalities of related structures are diagnosed with higher precision and surgical complications min

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Ilie, Adrian Cosmin, Adelina Maria Jianu, Mugurel Constantin Rusu, and Alexandru Nicolae Mureșan. "Anatomical Changes in a Case with Asymmetrical Bilateral Maxillary Sinus Hypoplasia." Medicina 58, no. 5 (2022): 564. http://dx.doi.org/10.3390/medicina58050564.

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Background and Objectives: The maxillary sinus hypoplasia (MSH) is an occasional variation of the maxilla, occurring either unilaterally or bilaterally. Previous studies dealing with MSH have not detailed the consequent anatomical changes of the maxilla and adjacent fossae. Materials and Methods: A 58-year-old female case was scanned in Cone Beam Computed Tomography and found to have asymmetrical bilateral MSH, who was then further evaluated anatomically. Results: The maxillary sinuses were hypoplastic and had mild mucosal thickenings. The orbital floors were curved. The uncinate process and t

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Jun, Beom-Cho, Sun-Wha Song, Chan-Soon Park, Dong-Hee Lee, Kwang-Jae Cho, and Jin-Hee Cho. "The analysis of maxillary sinus aeration according to aging process; volume assessment by 3-dimensional reconstruction by high-resolutional CT scanning." Otolaryngology–Head and Neck Surgery 132, no. 3 (2005): 429–34. http://dx.doi.org/10.1016/j.otohns.2004.11.012.

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OBJECTIVE: To evaluate change of the maxillary sinus volume according to patient age and gender by using a 3-dimensional (3-D) reconstruction of computed tomography images. STUDY DESIGN AND SETTING: One hundred seventy-three people (totaling 238 maxillary sinuses) who had undergone paranasal sinus CT scan between December 2000 and November 2003 and had no evidence of inflammation or hypoplasia in the CT finding and had no specific history of paranasal sinus surgery or maxillofacial trauma were retrospectively analyzed. The 3-D reconstruction images were obtained by using a surface-rendering te

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Krzeski, Antoni, Dorota Kapiszewska-Dzedzej, Norbert P. Górski, and Iwona Jakubczyk. "Cystic Fibrosis in Rhinologic Practice." American Journal of Rhinology 16, no. 3 (2002): 155–60. http://dx.doi.org/10.1177/194589240201600306.

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Background Cystic fibrosis (CF) is the most common genetic lethal disorder that affects white populations. Chronic rhinosinusitis (CRS) with extensive nasal polyposis is one of the manifestations of CF. Methods The aim of this study was to determine the prevalence and extent of CRS in CF patients. Results The study indicated that the signs and symptoms of CRS were present in all patients with CF and they were more advanced than in the control group. The most severe inflammatory changes in the paranasal sinuses were detected in patients with the dF508 gene mutation type who suffered from CRS fo

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Bequignon, Emilie, Laurence Dupuy, Francoise Zerah-Lancner, et al. "Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary Dyskinesia." Journal of Clinical Medicine 8, no. 5 (2019): 619. http://dx.doi.org/10.3390/jcm8050619.

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To date, no study precisely described ear, nose and throat (ENT) disease in adults with primary ciliary dyskinesia (PCD) and its relationship with ciliary function/ultrastructure. A retrospective study of standardized ENT data (exam, audiogram, sinus Computed tomography (CT), and bacteriology) was conducted in 64 adults with confirmed PCD who were followed in two ENT reference centers. Rhinorrhoea and hearing loss were the main symptoms. Symptom scores were higher in older patients. Nasal endoscopy was abnormal in all patients except one, showing nasal polyps in one-third of the patients and s

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Matsushita, K., and H. Yamamoto. "Bilateral hypoplasia of the maxillary sinus: swelling of the nasal mucosa after periapical periodontitis." British Journal of Oral and Maxillofacial Surgery 55, no. 3 (2017): 324–25. http://dx.doi.org/10.1016/j.bjoms.2016.08.009.

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Athmananda, Chandana, Kowsthuba Narayan, and Praveen Unki. "Binder’s syndrome: a rare disease." International Journal of Contemporary Pediatrics 9, no. 10 (2022): 975. http://dx.doi.org/10.18203/2349-3291.ijcp20222430.

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Von Binder described a rare congenital developmental disorder in 1962. It is a developmental disorder which is affecting the maxillary anterior region and nasal complex (nose and jaw) hence he gave the name maxillonasal dysplasia. Binder gave six classical characteristic features: arhinoid face, maxillary hypoplasia, reduced or absent nasal bridge, malformation of nasal bones, hypertrophy of turbinates with atrophy of nasal mucosa, absent frontal sinus (not compulsory). We reported a 8 years old female child presented with complaints of history of bilateral hearing loss and stuttering noticed

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9

Orhan Soylemez, Umut Percem, and Basak Atalay. "Investigation of the accessory maxillary ostium: a congenital variation or acquired defect?" Dentomaxillofacial Radiology 50, no. 6 (2021): 20200575. http://dx.doi.org/10.1259/dmfr.20200575.

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Objective: We sought to determine whether an accessory maxillary ostium (AMO) is a congenital or acquired condition and we investigated concomitant sinus pathologies associated with this structure. Methods: Paranasal sinus CT examinations of individuals aged ≥13 years and <13 years were compared retrospectively. In total, 552 sinuses of 276 patients aged ≥13 years (Group 1) and 284 maxillary sinuses of 142 children aged <13 years (Group 2) were evaluated. Patients were classified as AMO-positive or -negative. The following features were evaluated in Group 1: AMO presence, mucus retention

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10

Rakheja, Dinesh, Golder N. Wilson, and Beverly B. Rogers. "Biochemical Abnormality Associated with Smith-Lemli-Opitz Syndrome in an Infant with Features of Rutledge Multiple Congenital Anomaly Syndrome Confirms that the Latter is a Variant of the Former." Pediatric and Developmental Pathology 6, no. 3 (2003): 270–77. http://dx.doi.org/10.1007/s10024-002-1116-4.

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We describe a female infant with morphologic features of Rutledge multiple-congenital-anomaly syndrome (RM-CAS) and biochemical features of Smith-Lemli-Opitz syndrome (SLOS). She had microcephaly with hypoplastic cerebral frontal lobes and cerebellum, agenesis of the splenium of corpus callosum, abnormal facies including hypertelorism with bilateral inner epicanthal folds, a broad nasal bridge with slightly anteverted nares and patent choanae, low set ears and complex conchal formation, high-arched palate and thick maxillary alveolar ridges, and micrognathia. Her chest was broad, genitalia wer

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