Department of Radiology, Gyeongsang National University School of Medicine and Gyeongsang National University Changwon Hospital, Changwon.
Department of Radiology, Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju.
Medicine (Baltimore). 2021 Mar 26;100(12):e25165. doi: 10.1097/MD.0000000000025165.
Rosai-Dorfman disease (RDD) is a rare and self-limiting condition caused by the non-neoplastic proliferation of histiocytes/phagocytes in the sinusoids of lymph nodes and in extranodal tissues. Of the extranodal involvement, laryngeal involvement is extremely rare. Because of its rarity and nonspecific clinicoradiologic features, RDD is often difficult to differentiate from other benign or malignant lymphoproliferative diseases. We present a case of RDD with infiltration of IgG4-bearing plasma cells manifesting laryngeal and nasal masses with cervical lymphadenopathy.
A 45-year-old male patient presented with recurrent epistaxis and airway disturbance.
On endoscopy, there were submucosal masses in both nasal cavities and both sides of subglottic larynx. On neck CT, there were well-defined, enhancing soft tissue masses in both nasal cavities and both sides of subglottic larynx, resulting in mild airway narrowing. In addition, multiple enlarged lymph nodes showing homogeneous enhancement were noted in both parotid glands and both internal jugular chains. All lesions demonstrated marked FDG-uptake on PET/CT. Therefore, the initial radiologic differential diagnoses included lymphoma and IgG4-related disease. Biopsy was performed on the nasal and laryngeal lesions, and they revealed RDD with infiltration of IgG4-bearing plasma cells.
The patient underwent surgical resection of the masses in the nasal cavity and larynx to relieve airway narrowing.
After surgery, airway obstruction was much improved and the patient was asymptomatic. On outpatient follow-up, he exhibited a stable condition and had no dyspnea on exercise.
Clinical awareness and suspicion are important for the accurate diagnosis and management of patients with homogeneous masses in the larynx or nasal cavity, even if there is no combined cervical lymphadenopathy.
罗道尔夫-多夫曼病(RDD)是一种罕见的、自限性疾病,由淋巴结窦和结外组织中的组织细胞/吞噬细胞的非肿瘤性增殖引起。在结外受累中,喉部受累极为罕见。由于其罕见性和非特异性临床影像学特征,RDD 常难以与其他良性或恶性淋巴增生性疾病相区别。我们报告了一例 IgG4 阳性浆细胞浸润的 RDD 病例,表现为喉和鼻肿块伴颈淋巴结病。
一名 45 岁男性患者因反复鼻出血和气道障碍就诊。
内镜检查发现双侧鼻腔和会厌下喉均有黏膜下肿块。颈部 CT 显示双侧鼻腔和会厌下喉均有边界清楚、增强的软组织肿块,导致气道轻度狭窄。此外,双侧腮腺和双侧颈内静脉链均可见多个均匀增强的增大淋巴结。所有病变在 PET/CT 上均显示出明显的 FDG 摄取。因此,最初的影像学鉴别诊断包括淋巴瘤和 IgG4 相关疾病。对鼻和喉部病变进行了活检,结果显示为 RDD,伴有 IgG4 阳性浆细胞浸润。
患者接受了鼻腔和喉部肿块的手术切除,以缓解气道狭窄。
手术后,气道阻塞明显改善,患者无症状。门诊随访时,患者病情稳定,运动时无呼吸困难。
对于喉或鼻腔内有均匀肿块的患者,即使无合并颈淋巴结病,临床意识和怀疑也很重要,这有助于准确诊断和管理。