Maiti Mousam, Dutta Mainak, Chakrabarti Indranil, Ali Henna, Mazumder Sujaya, Mukherjee Arundhati, Mallick Ajay
Department of Otorhinolaryngology and Head-Neck Surgery, All India Institute of Medical Sciences, Kalyani NH-34 Connector, Basantapur, Saguna, Kalyani, West Bengal, India.
Department of Burns and Plastic Surgery, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
Eur Arch Otorhinolaryngol. 2025 Sep 18. doi: 10.1007/s00405-025-09686-1.
To provide the clinico-radiologic and histopathologic illustration of a unique case of sinonasal intravascular papillary endothelial hyperplasia (IPEH; Masson's tumor).
Case report and review of literature.
A 29-year-old man presented with right-sided nasal obstruction and occasional blood-tinged mucopurulence for two years. Diagnostic naso-endoscopy revealed a fleshy polypoid mass occupying the right nasal cavity encroaching into the nasopharynx. The mass was tender and firm, and bled on touch. Gadolinium-enhanced magnetic resonance imaging done two months prior showed a large, heterogenous mass in the right nasal cavity, partly involving the maxillary sinus, and extending into the nasopharynx. The findings were corroborated in a recent contrast-enhanced computed tomography scan that revealed mild contrast uptake and bone remodeling due to expansile nature of the mass without any erosion. An infected antrochoanal polyp, vascular tumor, and neoplastic lesions (including inverted papilloma) were considered as differentials. A subsequent punch biopsy revealed histologic pictures suggestive of IPEH. The mass was excised completely through endonasal endoscopic approach, and it was found to originate from the right inferior turbinate. The final histopathology confirmed the biopsy findings. Troublesome bleeding was encountered both during the biopsy and endoscopic excision of the mass. The patient is symptom-free with no recurrence at one-year follow-up.
Sinonasal IPEH (Masson's tumor) is an extremely rare entity; only 14 patients have been reported in the last four decades as evident from the PubMed/MEDLINE search. The present report adds to the existing literature, summarizes the clinico-radiologic and histopathologic perspectives, highlights the surgical challenges, and underlines the importance of having a low threshold of suspicion for considering this entity as a differential in a bleeding sinonasal mass.
提供一例独特的鼻窦血管内乳头状内皮增生(IPEH;马松瘤)病例的临床影像学和组织病理学例证。
病例报告及文献复习。
一名29岁男性,右侧鼻塞伴间断性血性黏液脓性分泌物两年。诊断性鼻内镜检查发现一个肉质息肉样肿物占据右侧鼻腔并侵入鼻咽部。肿物触之质韧、有触痛,触之易出血。两个月前的钆增强磁共振成像显示右侧鼻腔有一个大的、不均匀肿物,部分累及上颌窦,并延伸至鼻咽部。近期的对比增强计算机断层扫描结果证实了上述发现,显示肿物呈膨胀性生长,有轻度对比剂摄取及骨质重塑,但无骨质侵蚀。鉴别诊断考虑为感染性上颌窦后鼻孔息肉、血管性肿瘤及肿瘤性病变(包括内翻性乳头状瘤)。随后的穿刺活检显示组织学图像提示为IPEH。通过鼻内镜手术完全切除肿物,发现其起源于右下鼻甲。最终组织病理学检查证实了活检结果。活检及内镜切除肿物过程中均遇到棘手的出血情况。患者在一年随访期内无症状且无复发。
鼻窦IPEH(马松瘤)是一种极其罕见的疾病;从PubMed/MEDLINE搜索结果来看,过去40年仅报道了14例。本报告丰富了现有文献,总结了临床影像学和组织病理学观点,突出了手术挑战,并强调了对于鼻窦出血性肿物,应将该病作为鉴别诊断之一进行低阈值怀疑的重要性。