Miyamori Moeko, Ichikawa Takaya, Inamura Naoya, Takekawa Hana, Sakoda Kento, Yamada Kazuyuki, Suzuki Fumiyuki
Department of Otorhinolaryngology and Thyroid Surgery, Sapporo City General Hospital, Sapporo, Hokkaido 060-8604, Japan.
Department of Hematology, Sapporo City General Hospital, Sapporo, Hokkaido 060-8604, Japan.
Oncol Lett. 2024 Jan 30;27(3):132. doi: 10.3892/ol.2024.14265. eCollection 2024 Mar.
Primary haematological neoplasms of the larynx are uncommon; therefore, information regarding their epidemiology is limited and the diagnosis of histological types requires careful consideration. The current study describes the case of a 72-year-old male patient with primary laryngeal lymphoplasmacytic lymphoma (LPL) that was difficult to distinguish from plasmacytoma. Imaging examinations of the neck revealed a mass in the right laryngeal folds, 25×12×25 mm in size, which was surgically resected by direct laryngoscopy. Histopathologically, the mass showed diffuse proliferation of plasma cells with CD138 (+) and IgG (+) in the submucosal stroma. Flow cytometry revealed the tumour was positive for CD19 and negative for CD56. Based on these findings, the final diagnosis was confirmed as LPL, albeit similar to plasmacytoma regarding phenotypic features. There was no evidence of local or systemic recurrence following surgery, and the patient has been followed up without additional treatment. This case highlights the unique presentation of laryngeal lymphoma mimicking solitary plasmacytoma. The key factor in the diagnosis was the expression pattern of surface antigen markers.
原发性喉血液系统肿瘤并不常见;因此,关于其流行病学的信息有限,组织学类型的诊断需要仔细考虑。本研究描述了一例72岁男性原发性喉淋巴浆细胞淋巴瘤(LPL)患者,该病例难以与浆细胞瘤区分。颈部影像学检查显示右侧喉襞有一大小为25×12×25 mm的肿块,通过直接喉镜手术切除。组织病理学检查显示,肿块在黏膜下基质中表现为浆细胞弥漫性增殖,CD138(+)和IgG(+)。流式细胞术显示肿瘤CD19阳性,CD56阴性。基于这些发现,最终诊断为LPL,尽管在表型特征上与浆细胞瘤相似。术后无局部或全身复发证据,患者未接受额外治疗,一直在接受随访。该病例突出了喉淋巴瘤模仿孤立性浆细胞瘤的独特表现。诊断的关键因素是表面抗原标志物的表达模式。