Izadi Farzad, Ghanbari Hadi, Azizi Mohammad Reza, Gasembaglou Shahram, Manteghi Mohammad Javad, Ghanbari Azadeh
Department of Otorhinolaryngology, Hazart Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
ENT & HNS Research Center, Hazart Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
Iran J Otorhinolaryngol. 2016 Jan;28(84):79-82.
Inflammatory myofibroblastic pseudotumors are initially described in the lung and various extrapulmonary sites such as the orbits, palatine tonsils, ears, gingiva, pterygomaxillary space, and periodontal tissues. These tumors rarely involve the larynx and predilection to the glottis occurs in an indolent manner.
This case describes a laryngeal myofibroblastic tumor in a 46-year-old woman who presented with an aggressive tumor that extended to the floor of the mouth and the base of the tongue. Extended supraglottic laryngectomy was undertaken for the patient. The diagnosis was spindle cell proliferation with dense lymphoplasma cell infiltration compatible with inflammatory myofibroblastic tumor (Inflammatory pseudotumor or plasma cell granuloma). Definitive diagnosis was achieved with immunohistochemical (IHC) staining.
We believe that further IHC studies are required to define the true nature of these tumors especially for those that behave in an aggressive pattern.
炎性肌纤维母细胞性假瘤最初在肺部以及眼眶、腭扁桃体、耳部、牙龈、翼腭窝和牙周组织等各种肺外部位被描述。这些肿瘤很少累及喉部,且声门受累倾向呈惰性表现。
本病例描述了一名46岁女性的喉部肌纤维母细胞瘤,该肿瘤具有侵袭性,已扩展至口腔底部和舌根。对该患者实施了扩大声门上喉切除术。诊断为梭形细胞增生伴密集的淋巴浆细胞浸润,符合炎性肌纤维母细胞瘤(炎性假瘤或浆细胞性肉芽肿)。通过免疫组织化学(IHC)染色得以确诊。
我们认为需要进一步进行免疫组织化学研究以明确这些肿瘤的真实性质,尤其是对于那些具有侵袭性表现的肿瘤。