Haritharan T, Islah M, Zulfiqar A, Thambi Dorai C R
Department of Surgery, University Kebangsaan Malaysia, Jalan Yaacob Latiff, Bandar Tun Razak, Kuala Lumpur.
Med J Malaysia. 2006 Jun;61(2):258-9.
Isolated involvement of the clitoris by vascular malformation (VM) is very rare. Clinically, the lesion simulates female pseudohermaphroditism. A five-year-old girl presented with clitoromegaly and a clinical diagnosis of solitary VM of the clitoris was made. Magnetic resonance imaging showed characteristic features and confirmed the diagnosis and the extent of the VM. This is the first reported case of isolated involvement of the clitoris by VM to be diagnosed preoperatively.
血管畸形(VM)单独累及阴蒂极为罕见。临床上,该病变类似女性假两性畸形。一名五岁女孩出现阴蒂肥大,临床诊断为孤立性阴蒂VM。磁共振成像显示出特征性表现,证实了VM的诊断及其范围。这是首例术前诊断为VM单独累及阴蒂的报道病例。