Complete response of skull base inverted papilloma to chemotherapy: Case report.

IF 2.3 Q1 OTORHINOLARYNGOLOGY
Edward C Kuan, John W Frederick, Miguel F Palma Diaz, Dean W Lim, Jeffrey D Suh
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引用次数: 4

Abstract

Background: Inverted papilloma (IP) is the most common benign sinonasal neoplasm. Endoscopic techniques, improved understanding of pathophysiology, and novel surgical approaches have allowed rhinologists to treat IPs more effectively, with surgery being the mainstay of therapy. Frontal sinus IP poses a challenge for surgical therapy due to complex anatomy and potentially difficult surgical access.

Objectives: We reported a unique case of a massive frontal sinus IP that presented with intracranial and orbital extension, with near resolution after chemotherapy.

Methods: A retrospective case review of a patient with a frontal sinus IP treated at a tertiary academic medical center.

Results: A 75-year-old male patient presented with nasal obstruction, purulent nasal discharge, and a growing left supraorbital mass. Endoscopy demonstrated a mass that filled both frontal and ethmoid sinuses, with orbital invasion. There also was substantial erosion of the posterior table, which measured 1.73 × 1.40 cm. A biopsy specimen demonstrated IP with carcinoma in situ. The patient was deemed unresectable on initial evaluation and, subsequently, underwent chemotherapy (carboplatin and paclitaxel). The tumor had a dramatic response to chemotherapy, and the patient elected for definitive surgery to remove any residual disease. During surgery, only a small focus of IP was found along the superior wall of the frontal sinus. No tumor was found elsewhere, including at the site of skull base erosion. The final pathology was IP without carcinoma in situ or dysplasia.

Conclusion: This was the first reported case of chemotherapeutic "debulking" of IP, which facilitated surgical resection, despite substantial intracranial and orbital involvement. Although nearly all IPs can be treated surgically, rare cases, such as unresectable tumors, may benefit from systemic chemotherapy.

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颅底内翻性乳头状瘤化疗完全缓解1例。
背景:内翻性乳头状瘤是鼻窦最常见的良性肿瘤。内窥镜技术、对病理生理学的理解的提高和新的手术方法使鼻医生能够更有效地治疗IPs,手术是治疗的主要手段。额窦IP由于复杂的解剖结构和潜在的手术进入困难,对手术治疗提出了挑战。目的:我们报告了一例独特的额窦性IP,其表现为颅内和眼眶扩张,化疗后接近消退。方法:回顾性分析在三级学术医疗中心治疗的额窦IP患者的病例。结果:一名75岁男性患者表现为鼻塞、脓性鼻排出物及左侧眼眶上肿物。内窥镜显示一个肿块填满额窦和筛窦,并侵犯眼眶。后桌子也有大量的侵蚀,尺寸为1.73 × 1.40厘米。活检标本显示IP伴原位癌。在最初的评估中,患者被认为是不可切除的,随后接受了化疗(卡铂和紫杉醇)。肿瘤对化疗有明显的反应,患者选择最终手术切除任何残留的疾病。术中仅在额窦上壁发现一小块IP灶。其他部位未发现肿瘤,包括颅底侵蚀部位。最终病理为IP,无原位癌或不典型增生。结论:这是首次报道的IP化疗“减积”病例,尽管大量颅内和眼眶受累,但仍有助于手术切除。虽然几乎所有的IPs都可以手术治疗,但罕见的病例,如无法切除的肿瘤,可能受益于全身化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Allergy & Rhinology
Allergy & Rhinology OTORHINOLARYNGOLOGY-
CiteScore
3.30
自引率
4.50%
发文量
11
审稿时长
15 weeks
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