Marchioni Daniele, Alberti Chiara, Bisi Nicola, Rubini Alessia
Department of Otorhinolaryngology-Head and Neck Surgery, Azienda Ospedaliero-Universitaria di Modena, Via del Pozzo 71, 41125 Modena, Italy.
J Clin Med. 2024 Apr 24;13(9):2505. doi: 10.3390/jcm13092505.
: Petrous apex cholesterol granulomas (PACGs) are benign inflammatory cystic lesions of the temporal bone. Usually, asymptomatic patients may develop symptoms as the lesions expand. The diagnosis is based on both CT and MRI scans and the management relies on "wait and scan" or surgery. This paper aims at evaluating surgical outcomes and proposing a CT-based classification and a management algorithm. : Patients with PACGs who were surgically treated between 2014 and 2024 were included. Symptoms, imaging, approach type and complications were considered. CT scans were classified as Type A (preserved apex cellularity), Type B (erosion of the apex cellularity), and Type C (involvement of the noble structures bone boundaries). The possible connection of the lesion with the infracochlear, perilabyrinthine and sphenoidal cellularity was assessed. : Nineteen patients with symptoms like diplopia, headache and sensorineural hearing loss were included. According to our classification, 1/19 patients was Type A, 4/19 were Type B and 14/19 were Type C. Five patients underwent a total resection, seven a subtotal and seven a surgical drainage. Only two complications were recorded, and 17/19 patients showed symptom regression and stability during follow-up. : While the management of PACGs is still controversial, according to our classification and surgical outcomes, Type A, being mostly asymptomatic, should be managed with "wait and scan", Type B should undergo surgery when symptoms are present, while Type C should always undergo surgery because of their invasiveness and potential complications. When possible, a drainage should be attempted; otherwise, a surgical resection is chosen, and its completeness depends on the preoperative general and hearing status.
岩尖胆固醇肉芽肿(PACG)是颞骨的良性炎性囊性病变。通常,无症状患者可能会随着病变扩大而出现症状。诊断基于CT和MRI扫描,治疗方法取决于“观察并扫描”或手术。本文旨在评估手术效果,并提出基于CT的分类和治疗算法。
纳入2014年至2024年间接受手术治疗的PACG患者。考虑症状、影像学表现、手术方式和并发症。CT扫描分为A型(岩尖细胞结构保留)、B型(岩尖细胞结构侵蚀)和C型(侵犯重要结构骨边界)。评估病变与耳蜗下、迷路周围和蝶窦细胞结构的可能联系。
纳入19例出现复视、头痛和感音神经性听力损失等症状的患者。根据我们的分类,1/19例患者为A型,4/19例为B型,14/19例为C型。5例患者接受了全切除,7例次全切除,7例进行了手术引流。仅记录到2例并发症,17/19例患者在随访期间症状缓解且病情稳定。
虽然PACG的治疗仍存在争议,但根据我们的分类和手术结果,A型大多无症状,应采用“观察并扫描”的方法;B型在出现症状时应进行手术;而C型因其侵袭性和潜在并发症应始终进行手术。可能的情况下,应尝试进行引流;否则,选择手术切除,切除的完整性取决于术前的一般情况和听力状况。