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Artykuły w czasopismach na temat „Frontal sinus hypoplasia”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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1

Al Hatmi, Asma Sulaiman, Eiman Al Ajmi, Halima Albalushi, Meetham Al Lawati, and Srinivasa Rao Sirasanagandla. "Anatomical variations of the frontal sinus: A computed tomography-based study." F1000Research 12 (August 31, 2023): 71. http://dx.doi.org/10.12688/f1000research.129498.2.

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Background: The pneumatization of the frontal sinus is variable between individuals, including monozygotic twins. The volumetric anatomic variants of the frontal sinus are classified into aplasia, hypoplasia, medium-sized, and hyperplasia. We aimed to study the frontal sinus morphology in Omani patients using computed tomography (CT) evaluations. Methods: Retrospectively, 1220 frontal sinus CT scans from 610 patients investigated at Sultan Qaboos University Hospital, Oman, from January 2019 to December 2020 were reviewed. The frontal sinus morphology was classified according to the classificat
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Al Hatmi, Asma Sulaiman, Eiman Al Ajmi, Halima Albalushi, Meetham Al Lawati, and Srinivasa Rao Sirasanagandla. "Anatomical variations of frontal sinus pneumatization: A computed tomography-based study." F1000Research 12 (January 18, 2023): 71. http://dx.doi.org/10.12688/f1000research.129498.1.

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Background: The pneumatization of the frontal sinus is variable between individuals, including monozygotic twins. The volumetric anatomic variants of the frontal sinus are classified into aplasia, hypoplasia, medium-sized, and hyperplasia. We aimed to study the frontal sinus morphology in Omani patients using computed tomography (CT) evaluations. Methods: Retrospectively, 1220 paranasal sinus CT scans from 610 patients investigated at Sultan Qaboos University Hospital, Oman, from January 2019 to December 2020 were reviewed. The frontal sinus morphology was classified according to the classific
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Ozcan, Kursat Murat, Omer Hizli, Zeynep Alev Sarisoy, Hakan Ulusoy, and Guven Yildirim. "Coexistence of frontal sinus hypoplasia with maxillary sinus hypoplasia: a radiological study." European Archives of Oto-Rhino-Laryngology 275, no. 4 (2018): 931–35. http://dx.doi.org/10.1007/s00405-018-4892-9.

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Handa, Roopika, Soheyl Sheikh, P. Shambulingappa, et al. "Bilateral Absence of Frontal Sinus and Unilateral Mandibular Hypoplasia – A Case report." Bangladesh Journal of Dental Research & Education 5, no. 1 (2015): 29–32. http://dx.doi.org/10.3329/bjdre.v5i1.22459.

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Absence of frontal sinus is usually associated with various syndromes such as craniosynostosis, osteodysplasia, down syndrome etc. Geographically, absence of frontal sinus is seen usually in areas with cold climate. This paper reports a case of 18-year old Indian woman suffering from bilateral absence of frontal sinuses which was non-syndromic in conjunction with unilateral mandibular hypoplasia. The paper also highlights the clinical significance of frontal sinus which was non-syndromic absence and its rarity in warm climate such as in South East Asian regions and the treatment options of uni
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Joshi, Ankita, Chinmay Sundarray, and Krishna Arpita Sahoo. "Bilateral Total Aplasia of Paranasal Sinuses: A Rare Case Report." An International Journal Clinical Rhinology 8, no. 3 (2015): 124–26. http://dx.doi.org/10.5005/jp-journals-10013-1249.

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ABSTRACT Paranasal sinus anatomical anomalies with unknown etiology are common. Paranasal sinus-related diseases are associated with so high rate of morbidities, it becomes essential to identify the structure and pathophysiology of the paranasal sinuses. Computed tomography (CT) is a valuable tool in displaying its anatomy, any anatomic variations and diseases. As paranasal sinus development is a complex and long-lasting process, there are great structural variations between individuals. Maxillary and/or frontal sinus aplasia or hypoplasia are more common than the other types. Several degrees
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Karim, Soran M. "The prevalence of frontal sinus agenesis (aplasia) among Kurdish populations of Erbil city." Erbil Dental Journal 6, no. 2 (2023): 215–24. http://dx.doi.org/10.15218/edj.2023.23.

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Background and objective: The frontal bone contains a pair of air-filled hollow cavities called frontal sinuses, the size, shape and anatomic measurements and dimensions of the frontal sinuses are determined by the degree of its pneumatization. Any disturbance to the sinus during its early development stages could results whether in hypoplasia (underdevelopment) or aplasia (total lack) of the sinus either unilaterally or bilaterally. This study aims to investigate the prevalence of aplasia of the frontal sinus among Kurdish populations of Erbil city, in addition to assessment of the type of ap
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7

Haktanir, A., M. Acar, A. Yucel, A. Aycicek, B. Degirmenci, and R. Albayrak. "Combined sphenoid and frontal sinus aplasia accompanied by bilateral maxillary and ethmoid sinus hypoplasia." British Journal of Radiology 78, no. 935 (2005): 1053–56. http://dx.doi.org/10.1259/bjr/38163950.

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Tatlıpınar, Arzu, Onur Dede, Erkan Esen, Tanju Gökçeer, and Tayfun Akoğlu. "Combined sphenoid and frontal sinus aplasia accompanied by bilateral maxillary sinus hypoplasia in a child with sinusitis." International Journal of Pediatric Otorhinolaryngology Extra 6, no. 3 (2011): 149–52. http://dx.doi.org/10.1016/j.pedex.2010.06.002.

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Błochowiak, Katarzyna, and Bartłomiej Kamiński. "Combined aplasia of frontal and shenoid sinuses with hypoplasia of the maxillary sinus." European Journal of Clinical and Experimental Medicine 16, no. 2 (2018): 155–58. http://dx.doi.org/10.15584/ejcem.2018.2.12.

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Güven, Damla Güçlü, Süleyman Ylmaz, Sla Ulus, and Buğra Subaş. "Combined Aplasia of Sphenoid, Frontal, and Maxillary Sinuses Accompanied by Ethmoid Sinus Hypoplasia." Journal of Craniofacial Surgery 21, no. 5 (2010): 1431–33. http://dx.doi.org/10.1097/scs.0b013e3181ecc2d9.

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Kandogan, Tolga, Abdullah Dalgic, Hulya Mollamehmetoglu, and Ozgur Esen. "Combined Aplasia of Sphenoid, Frontal, and Maxillary Sinuses With Hypoplasia of The Ethmoid Sinus." Iranian Red Crescent Medical Journal 15, no. 1 (2013): 13–4. http://dx.doi.org/10.5812/ircmj.2627.

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Kang, Myeongsin, Jung-Hun Kown, Dong-Hyun Kim, Seung-Yoon Han, and Jae-Hoon Lee. "Sinonasal Anatomic Variations According to Frontal Sinus Pneumatization in a Korean Population." Korean Journal of Otorhinolaryngology-Head and Neck Surgery 64, no. 7 (2021): 473–78. http://dx.doi.org/10.3342/kjorl-hns.2020.00829.

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Background and Objectives It is necessary to understand the variations of the paranasal sinuses (PNS) and other anatomical structures during an endoscopic sinus surgery (ESS). The purpose of this study was to investigate any association between the degree of frontal sinus (FS) pneumatization and the development of the PNS structures. Subjects and Method We analyzed 311 PNS computed tomography (CT) scans (622 sinuses, including the left and right sides). We classified FS into type I (aplasia), type II (hypoplasia), and type III (control). We assessed and compared the middle turbinate pneumatiza
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13

Ghazizade, Matin, Mahboobe Asadi, and Pouyan Darbani. "Hypoplasia of the maxillary, sphenoid and frontal sinus in the patient with nasopharyngeal branchial cyst: Case Repor." Journal of Research in Medical and Dental Science 4, no. 4 (2016): 27. http://dx.doi.org/10.5455/jrmds.2016446.

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14

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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15

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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16

Pramanasari, Indra. "Dyke-Davidoff-Masson Syndrome (DDMS) in Adult: A Rare Case in Rural Area." AKSONA 3, no. 1 (2023): 26–30. http://dx.doi.org/10.20473/aksona.v3i1.38419.

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Highlight: Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures. The proper diagnosis and early causative treatment significantly improve the outcome of thee disease. ABSTRACT Introduction: Dyke-Davidoff-Masson syndrome (DDMS) could be a rare neurological disorder characterized by cerebral hemiatrophy and an engine shortfall on the contralateral side of the body. Furthermore, facial asymmetry and seizures are common symptoms. Classic imaging findings in individuals with DDMS a
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17

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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18

Rahayu, Fitriani Tri, Hexanto Muhartomo, Aditya Kurnianto, and Arinta Puspita Wati. "A Woman with Dyke-Davidoff-Masson Syndrome: A Case Report." Magna Neurologica 3, no. 2 (2025): 65–70. https://doi.org/10.20961/magnaneurologica.v3i2.1689.

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Introduction: Dyke-Davidoff-Masson Syndrome (DDMS) is a rare neurologic condition associated with drug-resistant epilepsy (DRE). Almost 100 DDMS cases were reported, and only 21 were reported among adults. This case report presented Dyke-Davidoff-Masson Syndrome in a 30-year-old woman. Case: A 30-year-old woman presented with generalized tonic-clonic seizures the day before admission. Each seizure lasted 5 minutes and reoccurred up to three times daily. She communicated but was slow in answering questions post-seizure. Neurological examination revealed left hemiparesis and contracture. Electro
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19

Morreale, P., S. Amato, P. Mannino, M. Sanfilippo, C. Comparato, and G. Scardino. "P53 DOUBLE OUTLET RIGHT VENTRICLE IN PATIENT WITH XP11.23 DUPLICATION AND SYNDROMIC PHENOTYPE: BROADENING OF THE CLINICAL SPECTRUM." European Heart Journal Supplements 25, Supplement_D (2023): D60. http://dx.doi.org/10.1093/eurheartjsupp/suad111.139.

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Abstract DORV accounts for 2–3% of congenital heart disease (prevalence of 1/10,000). It is a cono–truncal anomaly with variable clinic. In 25–42.5% of cases there are chromosomal anomalies such as trisomy 13, 18, 22q11 microdeletion and possible associated anomalies such as facial and skeletal dysmorphisms, brain anomalies and renal agenesis. duplication Xp11.22–p11.23 was described in 2009 by Giorda and is characterized by intellectual disabilities, speech delay, epilepsy, and EEG abnormalities. We report the case of a patient with dupXp11.23 and major anomalies not reported in the literatur
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20

Pajic, Srbislav S., Svetlana Antic, Arso M. Vukicevic, et al. "Trauma of the Frontal Region Is Influenced by the Volume of Frontal Sinuses. A Finite Element Study." Frontiers in Physiology 8 (July 11, 2017): Article 493. https://doi.org/10.3389/fphys.2017.00493.

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Anatomy of frontal sinuses varies individually, from differences in volume and shape to a rare case when the sinuses are absent. However, there are scarce data related to influence of these variations on impact generated fracture pattern. Therefore, the aim of this study was to analyse the influence of frontal sinus volume on the stress distribution and fracture pattern in the frontal region. The study included four representative Finite Element models of the skull. Reference model was built on the basis of computed tomography scans of a human head with normally developed frontal sinuses. By m
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Fang, Kuan-Chung, Ren-Wen Ho, Sheng-Dean Luo, Wei-Che Lin, Ching-Nung Wu, and Wei-Chih Chen. "Sinus Plain Film Can Predict a Risky Distance from the Lacrimal Sac to the Anterior Skull Base: An Anatomic Study of Dacryocystorhinostomy." Diagnostics 12, no. 4 (2022): 930. http://dx.doi.org/10.3390/diagnostics12040930.

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Background: Removal of the surrounding bone during dacryocystorhinostomy may present a higher risk of skull base injury in patients with frontal sinus aplasia. We used sinus plain films to predict cases with a greater risk of a reduced skull base distance in dacryocystorhinostomy. Methods: Sinus plain films and computed tomography data from patients were retrospectively evaluated. The frontal sinus was classified as normal, hypoplastic, or aplastic according to Waters’ view. Correlations of the frontal sinus roof-supraorbital margin (F-O) and the frontal sinus roof-nasion (F-N) distances on pl
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Lee, Dennis, Robin Brody, and Gady Har-El. "Frontal Sinus Outflow Anatomy." American Journal of Rhinology 11, no. 4 (1997): 283–86. http://dx.doi.org/10.2500/105065897781446720.

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Most of the studies of frontal sinus anatomy were completed 50 to 70 years ago. The information they provide is not necessarily relevant or helpful to the modem rhinologic surgeon who approaches the frontal sinus transnasally and endoscopically. We performed anatomical dissections of the outflow tract of 82 frontal sinuses in 41 cadaver heads to illustrate the various drainage patterns from the frontal sinus to the nose and to correlate these drainage sites with the distance and angle from the pyriform aperture. We found that the frontal sinus drained anterior to the uncinate process in 24 spe
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Meshram, SuwanshSukhadeorao, Sheetal Nikose, Shraddha Jain, and Amar Taksande. "Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation." Indian Journal of Human Genetics 20, no. 2 (2014): 189. http://dx.doi.org/10.4103/0971-6866.142899.

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Syed, Sajjad Ali Hashmi, Sadaf Tanveer Khan, and Jawwad Ali Hashmi Syed. "Use of Computed Tomography (CT scan) for delineating anatomy and variation of frontal Sinus before Functional Endoscopic Sinus Surgery." Perspectives in Medical Research 9, no. 3 (2022): 54–57. http://dx.doi.org/10.47799/pimr.0903.13.

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Abstract Introduction: For Functional Endoscopic Sinus Surgery (FESS), the surgeon needs an accurate depiction of the anatomy of paranasal sinuses and their variations. Computed tomography (CT Scan) fulfills this requirement by providing detailed anatomy, the anatomical variants, and the extent of the disease in and around the Para nasal sinuses. The aim of this study is to show the anatomy of the Frontal sinus as delineated by the computed tomography. Materials and Methods: STUDY DESIGN: Cross section Descriptive Study. Out of 337 patients above 12 years of age who were referred for computed
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Taori, Abhijeet, Divya Malpani, and Shrivardhan Malpani. "Spectrum of Anatomical Variations in Paranasal Sinuses Detected on Pre FESS CT PNS." Scholars Journal of Applied Medical Sciences 13, no. 06 (2025): 1319–20. https://doi.org/10.36347/sjams.2025.v13i06.013.

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Conventional radiography has been largely replaced by high-resolution CT scan of the paranasal sinuses (PNS) for evaluating congenital anatomical variations and sinus pathologies (1-3). In this retrospective study, we evaluated 1,450 CT scans of the paranasal sinuses to determine the prevalence of various anatomical variations. Patients aged 15 to 85 years were included, while those with bone destruction or distortion due to surgery, trauma, or other pathologies were excluded. The most common variation observed was a deviated nasal septum (DNS) in 603 cases (41.6%), followed by Agger nasi cell
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Taori, Abhijeet, and Divya Malpani. "Spectrum of Anatomical Variations in Paranasal Sinuses Detected on CT PNS Pre FESS." Scholars Journal of Applied Medical Sciences 6, no. 12 (2018): 5105–6. https://doi.org/10.36347/sjams.2018.v06i12.081.

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Conventional radiography has been largely replaced by high-resolution CT scan of the paranasal sinuses (PNS) for evaluating congenital anatomical variations and sinus pathologies [1-3]. In this retrospective study, we evaluated 1,450 CT scans of the paranasal sinuses to determine the prevalence of various anatomical variations. Patients aged 15 to 85 years were included, while those with bone destruction or distortion due to surgery, trauma, or other pathologies were excluded. The most common variation observed was a deviated nasal septum (DNS) in 603 cases (41.6%), followed by Agger nasi cell
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Kumbla, Pallavi A., Ashley Q. Thorburn, Jorge I. de la Torre, and René P. Myers. "Correction of Severe Frontal Bossing with Coronal Brow Lift and Osteoplastic Frontal Sinus Setback Aided by Virtual Surgical Planning: A Case Report." Craniomaxillofacial Trauma & Reconstruction Open 5 (January 1, 2020): 247275122097491. http://dx.doi.org/10.1177/2472751220974918.

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Objective: An 18 year old male with a hypoplastic midface, low anterior hairline, heavy brows and marked frontal bossing presented for evaluation. Laboratory evaluation for acromegaly was negative. He did have impairment of his bilateral visual fields as confirmed by visual field testing by ophthalmology. His nasal radix was also of particular concern to him as it formed a significantly depressed crease between his nasal bridge and his brow. He requested surgical correction of these deformities from both a functional and aesthetic standpoint. Methods: We performed thin-cut CT maxillofacial sca
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Carlos, Avian Loren C., and January E. Gelera. "Prevalence of Supraorbital Ethmoid Air Cells among Filipinos." Philippine Journal of Otolaryngology-Head and Neck Surgery 33, no. 2 (2018): 21–23. http://dx.doi.org/10.32412/pjohns.v33i2.261.

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 Objective : This study aims to determine the prevalence of supraorbital ethmoidal cells (SOEC) among Filipinos in a single tertiary government institution. 
 Methods:
 
 Study Design: Retrospective review of CT scan images
 Setting: Single Tertiary Institution
 Patients: 123 patients aged 13-years-old and above
 
 Results: A total of 474 CT scans (60 PNS and 414 Craniofacial) performed during the study period were considered, with 55 excluded for age < 13, and 296 excluded for craniofacial fractures. None had congenital craniofacial deformities. Eig
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Santos, Bianca Lemos dos, Maria Cecília Florisbal Damé, Ana Carolina Barreto Coelho, Plínio Aguiar Oliveira, Clairton Marcolongo-Pereira, and Ana Lucia Schild. "Lissencephaly-pachygyria and cerebellar hypoplasia in a calf." Ciência Rural 46, no. 9 (2016): 1622–28. http://dx.doi.org/10.1590/0103-8478cr20151572.

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ABSTRACT: A case of lissencephaly-pachygyria and cerebellar hypoplasia diagnosed in a Charolais x Tabapuã calf is described. The calf presented since birth, clinical signs characterized by apathy, prolonged recumbency, tremors of the head and neck, ataxia, hypermetria, difficulty walking, blindness and swelling of the joints of the four limbs. Due to the unfavorable prognosis, the animal was euthanized and necropsied at 34 days of age. At necropsy, a rudimentary development of the brain folds (gyri) and grooves (sulci) was observed, and the cerebellum was hypoplastic. The cut surface of the br
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Bhardwaj, Prashant, Abhinav Srivastava, Sadhana Yadav, and Amit K. Rana. "An unusual Case of Bilateral Ethmoidal Mucopyocele." International Journal of Advanced and Integrated Medical Sciences 1, no. 3 (2016): 135–38. http://dx.doi.org/10.5005/jp-journals-10050-10047.

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ABSTRACT Mucocele is defined as an epithelial-lined, mucus-containing benign sac completely filling the sinus and can be seen expanding to induce pressure effects on surrounding structures. Frontoethmoidal mucocele is by far the most common due to the complexity of its drainage, and incidence of maxillary mucocele is least. A 20-year-old female presented with a chief complaint of protruding right eyeball, redness and watering from both eyes, persistent headache, and decreased vision in both eyes since 4 months, along with complaint of diplopia and bilateral nasal obstruction with marked nonaxi
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Mielcarek-Kuchta, Daniela, Karolina Simon, Dawid Kondratowicz, Zofia Łukomska, and Aleksandra Rybak-Korytowska. "Functional endoscopic sinus surgery (FESS) in unilateral sinus disease." Otolaryngologia Polska 71, no. 5 (2017): 29–35. http://dx.doi.org/10.5604/01.3001.0010.5314.

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Background: Unilateral sinus disease (USD) occurs in 23 % of all cases. It is believed that it is mainly associated with cancer development. Retrospective data from large rhinological centers show that the most common USD is chronic rhinosinusitis (CRS), followed by mycosis, inverted papilloma and finally cancer, but only in a small percent of cases. The aim of the study: The analysis of USD in the group of patients who underwent FESS at the secondary referral center. Material and Method: The retrospective study of patients treated for USD in the Department of Otolaryngology in the Provincial
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Uzar, Tomasz, Izabela Szczerbal, Katarzyna Serwanska-Leja, et al. "Congenital Malformations in a Holstein-Fresian Calf with a Unique Mosaic Karyotype: A Case Report." Animals 10, no. 9 (2020): 1615. http://dx.doi.org/10.3390/ani10091615.

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A Holstein-Fresian calf with multiple congenital malformations was subjected postmortem to anatomical and genetic investigation. The calf was small (20 kg), had shortened limbs and was unable to stand up. It lived only 44 days. Detailed anatomical investigation revealed the following features: head asymmetry, the relocation of the frontal sinus and eye orbits, hypoplastic thymus without neck part, ductus Botalli, unfinished obliteration in umbilical arteries, and a bilateral series of tooth germs in the temporal region. Cytogenetic examination, performed on in vitro cultured fibroblasts, showe
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Iampreechakul, Prasert, Adisak Tanpun, Punjama Lertbusayanukul, and Somkiet Siriwimonmas. "Contralateral extensive cerebral hemorrhagic venous infarction caused by retrograde venous reflux into the opposite basal vein of Rosenthal in posttraumatic carotid-cavernous fistula: A case report and literature review." Interventional Neuroradiology 24, no. 5 (2018): 546–58. http://dx.doi.org/10.1177/1591019918776615.

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We describe a patient with traumatic carotid-cavernous fistula (CCF), subsequently developing contralateral extensive hemorrhagic venous infarction from retrograde venous reflux into the opposite basal vein of Rosenthal. A 54-year-old woman was involved in a motor vehicle accident and sustained severe traumatic brain injury. Two months later, she developed bilateral proptosis and audible bruit. Magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA) of the brain demonstrated the right direct CCF. Fluid-attenuated inversion recovery (FLAIR) images showed a small hyperintense a
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Lapeña, José Florencio F. "Primary Care Evaluation of the Nose and Paranasal Sinuses." Philippine Journal of Otolaryngology-Head and Neck Surgery 21, no. 1-2 (2006): 57–58. http://dx.doi.org/10.32412/pjohns.v21i1-2.847.

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Primary care evaluation of the nose and paranasal sinuses begins with inspection. The astute clinician will seldom miss the hyperemic nose and open-mouth breathing of nasal congestion, the “long-face” facies, infraorbital dark “shiners” and edema of decreased lymphatic drainage from chronic nasal obstruction, and the transverse nasal crease from repeated performance of the “allergic salute” in allergic rhinitis. Tearing may be caused by inferior obstruction of the nasolacrimal duct. Widening of the nasal bridge (Woake’s syndrome) may suggest massive nasal polyposis2. The patient with acute sin
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Balasubramanian, Thiagarajan, and Narashiman Seethalakshmi. "HYPOPLASIA OF ALL PARANASAL SINUSES A SERIES CASE REPORT AND LITERATURE REVIEW." Balasubramanian Thiagarajan, February 29, 2012. https://doi.org/10.5281/zenodo.811428.

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Hypoplasia of maxillary sinus is a rather rare condition. Review of literature reveal that so far only 6 cases have been reported. Hypoplasia of frontal and sphenoid sinuses has been documented rather frequently. In this article the authors report two rare cases of hypoplasia involving all paranasal sinuses which has not been reported so far in literature. This is actually an incidental finding when routine CT scan of sinuses was performed. This patient was clinically asymptomatic. Awareness of this condition is important because of implications involved in performing FESS surgery in these pat
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Ali, Babar, Zonaina Nadeem, Muhammad Naeem, et al. "Evaluation of the Frequency of Anatomic Variations of the Paranasal Sinus Region by Using Multidetector Computed Tomography: A Hospital‐Based Cross‐Sectional Study." Health Science Reports 8, no. 3 (2025). https://doi.org/10.1002/hsr2.70535.

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ABSTRACTBackground and AimsThe sinus anatomy should be well‐understood by the sinus surgeons to carry out functional endoscopic sinus surgery carefully. That's why CT scans are vital to provide essential clarity and accuracy for comprehensive presurgical planning with minimal risks. The aim of this study was to evaluate the frequency of anatomic variations of the paranasal sinus region by using multidetector computed tomography.MethodsA cross‐sectional study of one hundred and fifty‐three patients of all age groups was carried out in the radiology department of Shalamar Hospital Lahore from 20
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Grine, Frederick E., Victoria A. Greening, Emily Hernandez, Brendon K. Billings, Victor Mngomezulu, and Carrie S. Mongle. "Metopism in adult South Africans and its relationship to frontal sinus size." Anatomical Record, November 13, 2023. http://dx.doi.org/10.1002/ar.25350.

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AbstractThis study documents the incidences of complete and partial metopism and their possible relationship to frontal sinus volume (FSV) in a sample of modern adult black South Africans with a view to evaluating the hypothesis that metopism affects frontal sinus hypoplasia. FSV was measured from CT scans and the incidence of metopism was recorded from direct observations of dried cadaveric crania. The sex of each individual was known. Four linear cranial dimensions were used to compute a geometric mean by which to scale FSV. The incidence of partial metopism (38%) is comparable to that repor
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Gruszka, Katarzyna, Seçil Aksoy, Ingrid Różyło-Kalinowska, Melis Mısırlı Gülbeş, Paweł Kalinowski, and Kaan Orhan. "A comparative study of paranasal sinus and nasal cavity anatomic variations between the Polish and Turkish Cypriot Population with CBCT." Head & Face Medicine 18, no. 1 (2022). http://dx.doi.org/10.1186/s13005-022-00340-3.

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Abstract Background Genetic and environmental factors especially climatic conditions are thought to influence the shape and size of the paranasal sinuses and anatomic variations may create both a diagnostic and therapeutic challenge. However, no study has been published about the climatic adaptation of the paranasal sinus region in different populations. This study aimed to compare the prevalence of anatomical variants in the paranasal sinus and nasal cavity using Cone-Beam Computed Tomography (CBCT) between Polish and Turkish Cypriot populations. Methods The material consisted of volumes acqu
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Haerian, Hoda, Roshanak Ghaffari, and Shabnam Azari. "Investigating paranasal sinuses developmental disorders and septum deviation angle effects on olfactory fossa depth using cone-beam computed tomography." Dental Research Journal 21, no. 1 (2024). http://dx.doi.org/10.4103/drj.drj_50_23.

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ABSTRACT Background: The ethmoid roof separates the ethmoid cells from the anterior cranial fossa. From the medial side, the roof of the ethmoid is connected to the lateral lamella of the ethmoid plate, which is the thinnest bone at the base of the skull and is most vulnerable to damage during endoscopic surgeries. The purpose of this study is to investigate the height of the lateral lamella in patients with hypoplasia/aplasia of the paranasal sinuses and deviation of the nasal septum using reconstructed multiplanar images by cone-beam computed tomography (CBCT). Materials and Methods: In this
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Pandey, Sonia K., Christopher L. Kalmar, Christopher M. Bonfield, and Michael S. Golinko. "Frontal sinus hypoplasia in unoperated older patients with craniosynostosis: a pilot study." Child's Nervous System, May 3, 2023. http://dx.doi.org/10.1007/s00381-023-05927-y.

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Kiran, Rajkumar Swathi, Vellathussery C. Sunitha, Ravindar Kashyap, Ramachandran Madhan, Andi S. Ramesh, and Krishnan Nagarajan. "Atretic cephaloceles with different imaging phenotypes – Case series with review of literature." Journal of Neurosciences in Rural Practice, March 16, 2023, 1–4. http://dx.doi.org/10.25259/jnrp_46_2022.

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Atretic cephaloceles (ACs) are congenital skull defects with herniation of rudimentary intracranial structures through the defect and associated with persistent falcine sinus or embryonic positioning of straight sinus. We describe five cases of ACs, out of which only one had embryonic straight sinus. Three cases had other intracranial malformations such as hypoplasia of corpus callosum, dysplastic tectum in one child and parieto-occipital polymicrogyria with falcotentorial dehiscence in the other, and frontal horn deformity and cortical dysplasia in the third. The prognosis of AC depends on th
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"Combined sphenoid and frontal sinus aplasia accompanied by bilateral maxillary sinus hypoplasia in a child with sinusitis." International Journal of Pediatric Otorhinolaryngology 75, no. 5 (2011): 727. http://dx.doi.org/10.1016/j.ijporl.2010.06.017.

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Elvan, Özlem, Kaan Esen, Şükrü Hakan Kaleağasi, and Mesut Sabri Tezer. "Computed Tomography Evaluation of Frontal Sinus Volume in Migraine Patients." Journal of Craniofacial Surgery, May 9, 2024. http://dx.doi.org/10.1097/scs.0000000000010272.

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This study aimed to assess the frontal sinus volume (FSV) on computed tomography (CT) scans in migraine patients. Cranial and paranasal CT images from 75 migraine patients (mean age: 39.14±13.63 y) and 23 control cases (mean age: 38.78±13.32 y) were analyzed retrospectively. Three-dimensionally reconstructed images of frontal sinuses were generated. Total FSV, anterolateral, and transverse diameters of the head were measured. The presence/absence and nature of supraorbital foramen and notches were evaluated. The total FSV was 8.02±5.97 cm3 in the migraine group and 8.38±4.83 cm3 in the control
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Zabiulla, Ismail, and Manohar Kachare. "EVALUATION OF COMMON ANATOMICAL VARIANTS OF PARANASAL SINUSES AND THEIR FREQUENCY DEMONSTRATED BY MULTI-DETECTOR COMPUTED TOMOGRAPHY." INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH, September 1, 2023, 65–68. http://dx.doi.org/10.36106/ijsr/8007562.

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BACKGROUND: Paranasal sinuses are air lled spaces present within the skull and facial bones. Paranasal sinuses region anatomy is highly variable. Knowledge of these variations is very important for radiologists as well as endoscopic surgeons for preoperative evaluation to avoid damage to adjacent vital structures. CT is the best modality to delineate the sinus anatomy as well as soft tissue structures. Thus, this study was undertaken to evaluate the anatomical variations of paranasal sinus region and ascertain their clinical importance. Study population MATERIAL: of 100 patients who underwent
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"Thalassemia Major and related Dentomaxillofacial Complications: Clinical and Radiographic Overview with Reference to Dental Care." International Journal of Experimental Dental Science 6, no. 2 (2017): 95–104. http://dx.doi.org/10.5005/jp-journals-10029-1163.

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ABSTRACT Introduction Thalassemia is one of the most common genetic disorders worldwide and presents public health and social challenges in areas of high incidence. Thalassemia major (TM) type is associated with most severe clinical changes. Aim To evaluate dental and oromaxillofacial features of TM. Materials and methods The sample consisted of 54 children and adolescents with TM, 31 males and 23 females, aged 5.5 to 18.3 years (mean age 11.6 ± 3.2 years) and thalassemia-free controls. They were examined for dental caries, oral hygiene, periodontal status, orofacial features, tooth size and d
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Soltani, Parisa, Mahnaz Sheikhi, Mahsayeh Lashkarizadeh, Flavia Iaculli, and Gianrico Spagnuolo. "Bilateral Aplasia of the Frontal, Sphenoid and Maxillary Sinuses and Unilateral Aplasia of the Ethmoid Air Cells." Journal of Iranian Medical Council, October 23, 2022. http://dx.doi.org/10.18502/jimc.v5i3.10952.

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Background: Sporadic cases of sinus aplasia have been reported in the literature, but only a few cases of total aplasia of paranasal sinuses have been recorded. In this report, we aim to present a case of aplasia of all paranasal sinuses except for the right ethmoid sinus which was hypoplastic.
 Case Report: The patient was a 50-year-old female referred for obtaining Cone Beam Computed Tomography (CBCT) prior to dental implant placement. The patient was asymptomatic and did not have any complaints or discomforts associated with the craniofacial structures. CBCT views showed bilateral abse
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