Krebs Simone, Ganly Ian, Ghossein Ronald, Yang Joanna, Yahalom Joachim, Schöder Heiko
Department of Radiology, Molecular Imaging and Therapy Service, Memorial Sloan Kettering Cancer Center, New York, United States.
Department of Surgery, Head and Neck Service, Memorial Sloan Kettering Cancer Center, New York, United States.
Front Oncol. 2017 Nov 27;7:284. doi: 10.3389/fonc.2017.00284. eCollection 2017.
Solitary plasmacytoma (SP) is an extremely rare form of hematologic malignancy that can be classified as solitary bone plasmacytoma or solitary extramedullary plasmacytoma. Here, we report a patient who presented with progressive shortness of breath and foreign body sensation in his throat. Fluorodeoxyglucose positron emission tomography/computed tomography (F-FDG-PET/CT) demonstrated an abnormal FDG-avid soft tissue mass arising from the larynx involving the cricoid cartilage without additional suspicious lesions. Histology revealed an abundance of plasma cells; immunohistochemistry was positive for CD138 expression and lambda chains, and negative for CD20. Comprehensive imaging studies and panendoscopy of the ENT tract confirmed solitary disease involvement. Following additional systemic work-up, a diagnosis of extramedullary plasmacytoma was rendered. The patient underwent definitive radiotherapy using intensity-modulated radiation therapy (total dose of 46 Gy, divided in 23 fractions of 200 cGy). Serial PET/CT showed the stepwise resolution of abnormal FDG uptake and resolution of the cricoid cartilage lesion. With 22 months of follow-up, the patient remains free of disease. We describe the rare case of SP presenting as a FDG-avid hypermetabolic soft tissue mass in the cricoid cartilage, which should be considered in the differential diagnosis of laryngeal tumors. Of note, SP is radiosensitive; favorable outcome can be expected once treated with doses of 40-50 Gy. FDG PET/CT is helpful in diagnosis and response assessment for this disease.
孤立性浆细胞瘤(SP)是一种极为罕见的血液系统恶性肿瘤,可分为孤立性骨浆细胞瘤或孤立性髓外浆细胞瘤。在此,我们报告一名患者,其表现为进行性气短和咽喉部异物感。氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(F-FDG-PET/CT)显示,一个异常的FDG摄取增高的软组织肿块起源于喉部,累及环状软骨,未发现其他可疑病变。组织学检查显示大量浆细胞;免疫组化显示CD138表达及λ链呈阳性,CD20呈阴性。全面的影像学检查和耳鼻喉科的全景内镜检查证实为孤立性病变。经过进一步的全身检查,诊断为髓外浆细胞瘤。患者接受了调强放射治疗(总剂量46 Gy,分23次给予,每次200 cGy)。系列PET/CT显示异常FDG摄取逐步消退,环状软骨病变也得到缓解。经过22个月的随访,患者无疾病复发。我们描述了这例罕见的以环状软骨FDG摄取增高的高代谢软组织肿块为表现的SP病例,在喉肿瘤的鉴别诊断中应考虑到该病。值得注意的是,SP对放疗敏感;给予40 - 50 Gy的剂量治疗后有望获得良好的预后。FDG PET/CT有助于该病的诊断和疗效评估。