Díaz-Pérez J A, García-Ramírez C A, García-Vera J A, Melo-Uribe M A, Uribe C J
Grupo de Investigación en Patología Estructural, Funcional y Clínica, Universidad Industrial de Santander, Bucaramanga, Colombia.
Actas Dermosifiliogr. 2008 Jul-Aug;99(6):474-6.
Rhabdomyomatous mesenchymal hamartoma is an extremely rare congenital lesion, and very few cases have been reported even though its macroscopic and microscopic features make diagnosis easy. An 18-year-old woman consulted with a pedunculated mass in the medial region of her neck. The mass was surgically removed, and rhabdomyomatous mesenchymal hamartoma was diagnosed. The clinical, macroscopic, histologic, and immunochemical characteristics that allow diagnosis of this entity are discussed. Although association with congenital abnormalities is uncommon, this possibility should be assessed by the clinician.
横纹肌瘤性间叶性错构瘤是一种极其罕见的先天性病变,尽管其大体和显微镜下特征易于诊断,但报道的病例仍非常少。一名18岁女性因颈部内侧带蒂肿块前来就诊。该肿块经手术切除,诊断为横纹肌瘤性间叶性错构瘤。本文讨论了有助于诊断该疾病的临床、大体、组织学和免疫化学特征。虽然与先天性异常相关并不常见,但临床医生仍应评估这种可能性。