Madjidi A, Couly G
Department of Pediatric Maxillofacial Surgery and Stomatology, Necker-Enfants Malades Hospital, Paris, France.
Oral Surg Oral Med Oral Pathol. 1993 Sep;76(3):284-8. doi: 10.1016/0030-4220(93)90254-2.
We report six cases of heterotopic neuroglial tissue of the face. All cases appeared at birth with a laterofacial mass and, in most cases, a respiratory disorder. The initial diagnosis has frequently been lymphangioma. But the rapidly growing character of the mass with resistance to high dose corticoid therapy, the fluid aspect at computerized tomography imaging with no connection to the central nervous system, and the presence of cerebrospinal fluid at the needle puncture were the most helpful features in narrowing the differential diagnoses. Patients were treated by surgical removal of the mass. The pathologic study showed the presence of neuroglial tissue. The management of the patients is discussed. The thirteen previous cases reported in the literature and our six cases lead to a discussion on the embryologic origin of this rare entity--the cephalic neural crest.
我们报告6例面部异位神经胶质组织病例。所有病例均在出生时出现面侧肿物,多数病例伴有呼吸障碍。最初诊断常为淋巴管瘤。但肿物生长迅速且对高剂量皮质类固醇治疗耐药、计算机断层扫描成像显示为液性且与中枢神经系统无连接、穿刺时出现脑脊液,这些是缩小鉴别诊断范围最有用的特征。患者接受了肿物手术切除治疗。病理研究显示存在神经胶质组织。本文讨论了患者的治疗。文献中先前报道的13例病例及我们的6例病例引发了关于这种罕见实体——头部神经嵴胚胎学起源的讨论。