Lee Dong Hoon, Lim Sang Chul
Department of Otolaryngology-Head and Neck Surgery, Chonnam National University Medical School & Hwasun Hospital, Hwasun, Republic of Korea.
J Rhinol. 2025 Jul;32(2):104-107. doi: 10.18787/jr.2025.00032. Epub 2025 Jul 22.
Seromucinous hamartoma is a rare, benign epithelial tumor of the sinonasal tract, most commonly originating from the posterior nasal septum. Accurate diagnosis is essential due to its histopathological resemblance to low-grade sinonasal adenocarcinoma. This study aimed to evaluate the clinical characteristics, diagnostic considerations, and treatment outcomes of patients with seromucinous hamartoma treated at a single tertiary referral center.
We retrospectively reviewed the medical records of six patients with histologically confirmed seromucinous hamartoma treated between January 2010 and May 2025. Data collected included demographic characteristics, presenting symptoms, imaging findings, histopathological features, and surgical outcomes.
Six patients with a total of seven lesions were identified; one patient presented with bilateral nasal involvement. The mean age at diagnosis was 33.9 years, and four patients were female. The most common presenting symptom was nasal obstruction, followed by epistaxis and rhinorrhea. Lesions were primarily located on the nasal septum, while some involved the inferior turbinate and sphenoid sinus. All patients underwent complete transnasal endoscopic resection. No recurrences were observed over a mean follow-up period of 58.6 months. One patient required medial maxillectomy due to difficulty distinguishing the lesion from adenocarcinoma.
Seromucinous hamartoma may arise at atypical sites and can mimic malignant tumors. Awareness of its variable presentation, along with complete surgical excision, is essential for optimal management and to avoid unnecessarily aggressive treatment.
浆液黏液性错构瘤是一种罕见的鼻窦良性上皮性肿瘤,最常见于鼻中隔后部。由于其组织病理学表现与低级别鼻窦腺癌相似,准确诊断至关重要。本研究旨在评估在一家三级转诊中心接受治疗的浆液黏液性错构瘤患者的临床特征、诊断要点及治疗结果。
我们回顾性分析了2010年1月至2025年5月期间6例经组织学确诊为浆液黏液性错构瘤患者的病历。收集的数据包括人口统计学特征、临床表现、影像学表现、组织病理学特征及手术结果。
共确诊6例患者,有7个病灶;1例患者双侧鼻腔受累。诊断时的平均年龄为33.9岁,4例为女性。最常见的临床表现为鼻塞,其次是鼻出血和鼻溢液。病灶主要位于鼻中隔,部分累及下鼻甲和蝶窦。所有患者均接受了经鼻内镜完整切除。平均随访58.6个月,未观察到复发。1例患者因难以将病灶与腺癌区分而需要行上颌骨内侧切除术。
浆液黏液性错构瘤可能发生于非典型部位,且可类似恶性肿瘤。认识其多样的表现形式,并进行完整的手术切除,对于优化治疗及避免不必要的过度治疗至关重要。