块状动脉假性动脉瘤:一种罕见的正颌外科并发症

Enrico Nastro Siniscalchi , Luciano Maria Catalfamo , Emanuele Magaudda , Gianmaria Mancini , Sergio Lucio Vinci , Giorgio Lo Giudice
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引用次数: 0

摘要

假性动脉瘤很少在正颌手术后发生,可引起面部肿胀、迟发性出血和搏动性软块等症状。本报告的目的是强调一个病例的咬肌动脉假性动脉瘤后,正颌手术,描述可能而罕见的发生和治疗。术后第9天,出现持续的面部肿胀和口腔内手术伤口和鼻子出血,随后出现晕厥。给予支持治疗,并要求进行血管ct检查。扫描结果引起了假性动脉瘤存在的怀疑。稳定临床图像后,进行治疗性血管造影。假性动脉瘤扩张记录在左咬肌动脉远端部分,并立即从主圈排除。该动脉作为一种解剖学变体,起源于起源于上颌内动脉的共同分支。虽然该并发症在创伤学中更为常见,但在可疑术中出血、持续面部肿胀和晚发性鼻口出血的病例中,颌面区假性动脉瘤应被认为是正颌手术的可能并发症。
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Masseteric artery pseudoaneurysm: A rare complication in orthognatic surgery

Pseudoaneurysm rarely develops after orthognathic surgery, and can cause symptoms such as facial swelling, delayed bleeding, and development of a pulsatile soft mass. The aim of this report is to highlight a case of a masseteric artery pseudoaneurysm following orthognatic surgery, describing the possible while rare occurrence and its treatment. At the ninth postoperative day, persistent facial swelling and bleeding from the intraoral surgical wounds and nose occurred, followed by a syncope. Support therapy was administered, and an Angio-CT was requested. The results of the scans raised suspicion of the presence of a pseudoaneurysm. After the stabilization of the clinical picture a therapeutic angiography was performed. A pseudoaneurysmatic dilatation was documented in the distal portion of the left masseteric artery and was promptly excluded from the main circle. This artery derived, as an anatomical variant, from a common branch originating from the internal maxillary artery. While this complication is more commonly reported in traumatology, in cases of suspicious intraoperative bleeding, persistent facial swelling, and late-onset nasal-oral hemorrhage, pseudoaneurysms of the maxillofacial district should be considered as a possible complication of orthognatic surgery.

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来源期刊
Oral and Maxillofacial Surgery Cases
Oral and Maxillofacial Surgery Cases Medicine-Otorhinolaryngology
CiteScore
0.60
自引率
0.00%
发文量
43
审稿时长
69 days
期刊介绍: Oral and Maxillofacial Surgery Cases is a surgical journal dedicated to publishing case reports and case series only which must be original, educational, rare conditions or findings, or clinically interesting to an international audience of surgeons and clinicians. Case series can be prospective or retrospective and examine the outcomes of management or mechanisms in more than one patient. Case reports may include new or modified methodology and treatment, uncommon findings, and mechanisms. All case reports and case series will be peer reviewed for acceptance for publication in the Journal.
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