Hansen T, Burg J E, Koutsimpelas D, Mann W J, Kirkpatrick C J
Institute of Pathology, Johannes Gutenberg-University of Mainz.
Mund Kiefer Gesichtschir. 2005 May;9(3):184-7. doi: 10.1007/s10006-005-0608-6.
Adult rhabdomyoma is a rare mesenchymal tumor, which generally grows slowly and is mainly localized in the head and neck area.
We report the extraordinary case of a rapidly growing adult rhabdomyoma in a 73-year-old man. The patient was treated for diffuse large B-cell non-Hodgkin's lymphoma with CHOP therapy (doxorubicin, cyclophosphamide, vincristine, and prednisone). Comparison of the respective computed tomography scans showed prominent enlargement of 35% in the tumor mass volume on the right side of the neck within 3 months. The tumor was highly suspicious for lymphoma. Surgical resection was performed.
Histological examination revealed a tumor which was composed of tightly packed polygonal cells with a PAS-positive granular or vacuolated cytoplasm, occasionally with cross-striations. Immunohistochemically, the cells were positive for desmin, myogenin, Myo-D1, but negative for S-100. Due to these characteristic morphologies, adult rhabdomyoma was diagnosed.
This is the first report on an adult rhabdomyoma with a proven rapid enlargement. The possible pathomechanisms are discussed.
成人横纹肌瘤是一种罕见的间叶组织肿瘤,通常生长缓慢,主要位于头颈部区域。
我们报告了一例73岁男性快速生长的成人横纹肌瘤的特殊病例。该患者接受了CHOP方案(多柔比星、环磷酰胺、长春新碱和泼尼松)治疗弥漫性大B细胞非霍奇金淋巴瘤。对比各自的计算机断层扫描显示,3个月内颈部右侧肿瘤体积显著增大35%。该肿瘤高度怀疑为淋巴瘤。遂进行了手术切除。
组织学检查显示肿瘤由紧密排列的多边形细胞组成,细胞质呈PAS阳性颗粒状或空泡状,偶尔可见横纹。免疫组化显示,细胞结蛋白、肌细胞生成素、Myo-D1阳性,但S-100阴性。基于这些特征性形态,诊断为成人横纹肌瘤。
这是首例经证实快速增大的成人横纹肌瘤报告。文中讨论了可能的发病机制。