Dehner L P, Chen K T
Arch Otolaryngol. 1978 Jul;104(7):399-403. doi: 10.1001/archotol.1978.00790070037010.
Embryonal rhabdomyosarcoma of the middle ear-mastoid is a highly lethal neoplasm of childhood in most cases, which clinically simulates a chronic infection. Extensive hemorrhage and necrosis in the biopsy specimen may obscure and often delay the diagnosis. Two of the six embryonal rhabdomyosarcomas in this study showed histologic evidence of differentiation. These same two patients were the only long-term survivors. Similar examples of "differentiated" embryonal rhabdomyosarcomas of the middle ear-mastoid with prolonged survival have been recorded individually in the literature. Therapeutic implications of this finding have been discussed.
中耳-乳突胚胎性横纹肌肉瘤在大多数情况下是一种儿童期高致死性肿瘤,临床上常表现为慢性感染。活检标本中的广泛出血和坏死可能会掩盖并常常延误诊断。本研究中的6例胚胎性横纹肌肉瘤中有2例显示出分化的组织学证据。同样是这两名患者是仅有的长期存活者。文献中也曾分别记录过中耳-乳突“分化型”胚胎性横纹肌肉瘤患者长期存活的类似病例。本文已讨论了这一发现的治疗意义。