Magid M S, Campbell W G, Ngadiman S, Godwin T A, Ward R
Department of Pathology, New York Hospital-Cornell Medical Center, New York 10021, USA.
Pediatr Pathol Lab Med. 1997 Mar-Apr;17(2):303-13.
We report a case of an infantile myofibromatosis with hemangiopericytoma-like features arising in the tongue of a 5-month-old female infant. Many authors now classify neoplasms as infantile myofibromatosis that were previously called infantile hemangiopericytoma. The ultrastructural features of our tumor illustrate its biphasic nature and provide a possible explanation for its histogenesis. Infantile myofibromatosis, including those diagnosed as infantile hemangiopericytomas, rarely arise in any intraoral location. Despite the generally good prognosis associated with these neoplasms, complete surgical excision is recommended to avoid recurrences.
我们报告了一例发生于一名5个月大女婴舌部的具有血管外皮细胞瘤样特征的婴儿肌纤维瘤病。现在许多作者将以前称为婴儿血管外皮细胞瘤的肿瘤归类为婴儿肌纤维瘤病。我们肿瘤的超微结构特征说明了其双相性质,并为其组织发生提供了一种可能的解释。婴儿肌纤维瘤病,包括那些被诊断为婴儿血管外皮细胞瘤的,很少发生于任何口腔内部位。尽管这些肿瘤通常预后良好,但仍建议完整手术切除以避免复发。