Völker Hans-Ullrich, Scheich Matthias, Höller Sylvia, Ströbel Philipp, Hagen Rudolf, Müller-Hermelink Hans Konrad, Eck Matthias
Institute of Pathology, University, Josef-Schneider-Str,2, 97080 Würzburg, Germany.
Diagn Pathol. 2007 Jan 9;2:1. doi: 10.1186/1746-1596-2-1.
Spindle cell tumors of the larynx are rare. In some cases, the dignity is difficult to determine. We report two cases of laryngeal spindle cell tumors.
Case 1 is a spindle cell carcinoma (SPC) in a 55 year-old male patient and case 2 an inflammatory myofibroblastic tumor (IMT) in a 34 year-old female patient. A comprehensive morphological and immunohistochemical analysis was done. Both tumors arose at the vocal folds. Magnified laryngoscopy showed polypoid tumors. After resection, conventional histological investigation revealed spindle cell lesions with similar morphology. We found ulceration, mild atypia, and myxoid stroma. Before immunohistochemistry, the dignity was uncertain. Immunohistochemical investigations led to diagnosis of two distinct tumors with different biological behaviour. Both expressed vimentin. Furthermore, the SPC was positive for pan-cytokeratin AE1/3, CK5/6, and smooth-muscle actin, whereas the IMT reacted with antibodies against ALK-1, and EMA. The proliferation (Ki67) was up to 80% in SPC and 10% in IMT. Other stainings with antibodies against p53, p21, Cyclin D1, or Rb did not result in additional information. After resection, the patient with SPC is free of disease for seven months. The IMT recurred three months after first surgery, but no relapses were found eight months after resurgery.
Differential diagnosis can be difficult without immunohistochemistry. Therefore, a comprehensive morphological and immunohistochemical analysis is necessary, but markers of cell cycle (apart from the assessment of proliferation) do not help.
喉的梭形细胞瘤很罕见。在某些情况下,其性质难以确定。我们报告两例喉梭形细胞瘤病例。
病例1是一名55岁男性患者的梭形细胞癌(SPC),病例2是一名34岁女性患者的炎性肌成纤维细胞瘤(IMT)。进行了全面的形态学和免疫组织化学分析。两个肿瘤均发生于声带。放大喉镜检查显示息肉样肿瘤。切除后,常规组织学检查显示形态相似的梭形细胞病变。我们发现有溃疡、轻度异型性和黏液样间质。在进行免疫组织化学检查之前,其性质尚不确定。免疫组织化学检查确诊为两种具有不同生物学行为的不同肿瘤。两者均表达波形蛋白。此外,SPC对全细胞角蛋白AE1/3、CK5/6和平滑肌肌动蛋白呈阳性,而IMT与抗ALK-1和EMA抗体反应。SPC的增殖指数(Ki67)高达80%,IMT为10%。用抗p53、p21、细胞周期蛋白D1或Rb抗体进行的其他染色未提供更多信息。切除后,SPC患者已无病生存7个月。IMT在首次手术后3个月复发,但再次手术后8个月未发现复发。
没有免疫组织化学检查,鉴别诊断可能会很困难。因此,全面的形态学和免疫组织化学分析是必要的,但细胞周期标志物(除了增殖评估)并无帮助。