THE JEDNOSTRANA HOANALNA ATREZIJA U ODRASLOM DOBU: PRIKAZ SLUČAJA

  • Anđelina Jovanović otorinolaringolog, Kliničko- bolnički centar Zemun
Ključne reči: jednostrana hoanalana atrezija, kongenitalna anomalija, devijacija nosne pregrade

Sažetak


Uvod Hoanalna atrezija je retka anomalija nosne šupljine, koja je u polovini slučajeva povezana sa drugim urođenim malformacijama. Dijagnoza se u najčešće postavlja po rođenju, ali zakasnele dijagnoze nisu retkost u praksi.

          Prikaz slučaja Prikazujemo slučaj pacijentkinje sa višegodišnjim otežanim disanjem na levu nozdrvu, pojačanom sekrecijom iz nosa i učestalim glavoboljama. U toku preoperativne pripreme, kompjuterizovanom tomografijom paranazalnih šupljina, utvrđena je levostrana hoanalna atrezija i opstrukcija u regiji levog osteomeatalnog kompleksa, a potom uspešno rešena modernim hirurškim pristupom. Kontrolni pregled, uz pomoć endoskopa, obavljen  je mesec dana od operacije, ukazao je da su obe hoane prohodne. Hoanalna atrezija može biti izolovana kranio facijalana malformacija ali i udružena u okviru sindroma. Bilateralne su inkompatibilne sa životom a unilaterlne mogu ispoljiti različitu simptomatologiju u zavisnosti od vrste atrezije i starosti pacijenta.

          Zaključak Dijagnoza se postavlja kliničkim otorinolaringološkim pregledom, endoskopijom nosa i kompjuterizovanom tomografijom paranazalnih sinusa i baze lobanje. Terapija je hirurška.

Reference

[1] Sutikno B, Thaufiqurrakhman M. Transnasal endoscopic neochoanal technique: an effective procedure for bilateral choanal atresia in adult female. Int J Surg Case Rep. 2021;86(6):106338. doi:10.1016/j.ijscr.2021.106338,  PMID: 34454213[2] Abdul Cader SH, Shah FA, Reghunandanan N. Clinical retrospective analysis of 15 cases of choanal atresia - our experience. World J. Otorhinolaryngol. Head Neck Surg. 2019;5(4):188–192, doi.org/10.1016/j.wjorl.2019.03.003[3] Durmaz CD, Taş V, Kocaay P, Fitöz ÖS, Onay H, Beton S, Özkınay F, Ilgın Ruhi H. Bilateral choanal atresia in an adult woman with pycnodysostosis. Congenit Anom (Kyoto). 2017;57(3):91-92. doi: 10.1111/cga.12204, PMID: 27933642.[4] Anajar S, Hassnaoui J, Rouadi S, Abada R, Roubal M, Mahtar M. A rare case report of bilateral choanal atresia in an adult. Int J Surg Case Rep. 2017;37:127–129. doi:10.1016/j.ijscr.2017.05.002, PMID: 28667919[5] Ramsden JD, Campisi P, Forte V. Choanal atresia and choanal stenosis. Otolaryngol Clin North Am. 2009;42(2):339–352. doi:10.1016/j. otc.2009.01.001,  PMID: 19328897. [6] Kurosaka H, Wang Q, Sandell L, Yamashiro T, Trainor PA. Rdh10 loss-of-function and perturbed retinoid signaling underlies the etiology of choanal atresia. Hum Mol Genet. 2017;26(7):1268-1279. doi: 10.1093/hmg/ddx031, PMID: 28169399.[7] Liktor B, Csokonai LV, Gerlinger I. A new endoscopic surgical method for unilateral choanal atresia. Laryngoscope. 2001;111(2):364-6. doi: 10.1097/00005537-200102000-00033, PMID: 11210891.[8] Kurosaka H. Choanal atresia and stenosis: Development and diseases of the nasal cavity. Wiley Interdiscip Rev Dev Biol. 2019;8(1):e336. doi: 10.1002/wdev.336. [9] Georgiopoulos C, Postler M, Rombaux P, Gudziol V, Abolmaali N, Hummel T. Unilateral Choanal Atresia: Indications of Long-Term Olfactory Deficits and Volumetric Brain Changes Postsurgically. ORL J Otorhinolaryngol Relat Spec. 2022;84(2):89-92. doi: 10.1159/000520188, PMID: 34839294.[10] Riepl R, Scheithauer M, Hoffmann TK, Rotter N. Transnasal endoscopic treatment of bilateral choanal atresia in newborns using balloon dilatation: own results and review of literature. Int J Pediatr Otorhinolaryngol. 2014;78(3):459-64. doi: 10.1016/j.ijporl.2013.12.017, PMID: 24445248. [11] De Vincentiis GC, Panatta ML, De Corso E, Marini G, Bianchi A, Giuliani M, Sitzia E, Tucci FM. Endoscopic treatment of choanal atresia and use of balloon dilation: our experience. Acta Otorhinolaryngol Ital. 2020;40(1):44-49. doi: 10.14639/0392-100X-1567, PMID: 32275648.[12] Agha RA, Franchi T, Sohrabi C, Mathew G, Kerwan A; SCARE Group. The SCARE 2020 Guideline: Updating Consensus Surgical CAse REport (SCARE) Guidelines. Int J Surg. 2020;84:226-230. doi: 10.1016/j.ijsu.2020.10.034, PMID: 33181358.[13] Patel VA, Ramadan J, Carr MM. Congenital Choanal Atresia Repair: An Analysis of Adverse Perioperative Events. Otolaryngol Head Neck Surg. 2018;159(5):920-926. doi: 10.1177/0194599818797282, PMID: 30149770. [14] Meleca JB, Anne S, Hopkins B. Reducing the need for general anesthesia in the repair of choanal atresia with steroid-eluting stents: A case series. Int J Pediatr Otorhinolaryngol. 2019;118:185-187. doi: 10.1016/j.ijporl.2019.01.004, PMID: 30639990.[15] Kancherla V, Romitti PA, Sun L, Carey JC, Burns TL, Siega-Riz AM, Druschel CM, Lin AE, Olney RS; National Birth Defects Prevention Study. Descriptive and risk factor analysis for choanal atresia: The National Birth Defects Prevention Study, 1997-2007. Eur J Med Genet. 2014;57(5):220-9. doi: 10.1016/j.ejmg.2014.02.010, PMID: 24576610.(16] Moreddu E, Rossi ME, Nicollas R, Triglia JM. Prognostic Factors and Management of Patients with Choanal Atresia. J Pediatr. 2019;204:234-239.e1. doi: 10.1016/j.jpeds.2018.08.074, PMID: 30291020.

Objavljeno
2023/08/07
Rubrika
Prikaz bolesnika