Dange N, Bonde V, Goel A, Muzumdar D
Department of Neurosurgery, Seth Gordhandas Sunderdas Medical College and King Edward VII Memorial Hospital, Mumbai, India.
Pediatr Neurosurg. 2007;43(6):522-5. doi: 10.1159/000108800.
A 7-year-old boy with Goldenhar syndrome was diagnosed to have a posterior cranial fossa dermoid cyst. The presence of such a combination of clinical entities has not been reported earlier. The embryonic dysgenesis causing midline posterior fossa dermoid and other anomalies observed in Goldenhar syndrome occur between the third and fifth week of intrauterine life and are probably interrelated. This report emphasizes the need for a high index of suspicion and the value of cranial imaging in a case with Goldenhar syndrome.
一名患有Goldenhar综合征的7岁男孩被诊断出患有颅后窝皮样囊肿。此前尚未有过这种临床病症组合的报道。导致颅后窝中线皮样囊肿及在Goldenhar综合征中观察到的其他异常的胚胎发育异常发生在子宫内生活的第3至5周,且可能相互关联。本报告强调了对于Goldenhar综合征病例需保持高度怀疑指数以及头颅成像的价值。