PDF(Pubmed)
Abstract：
Sarcomas, tumors of mesenchymal origin, comprise a small percentage of all malignant tumors and are often challenging to diagnose. Leiomyosarcoma (LMS) is a rare form of cancer arising from smooth muscle cells. While a soft tissue sarcoma diagnosis is rare in and of itself, LMS diagnosis at an adolescent age is even more unique. Vulvar LMS can easily be misdiagnosed as a benign vaginal lesion, leading to a delay in proper treatment and poorer outcomes. In this case, we present a 14-year-old female who was diagnosed with a grade 2 vulvar LMS that clinically mimicked a Bartholin\'s gland cyst.
摘要：
肉瘤,间质起源的肿瘤，占所有恶性肿瘤的一小部分，通常难以诊断。平滑肌肉瘤（LMS）是一种罕见的由平滑肌细胞引起的癌症。虽然软组织肉瘤的诊断本身很少见，青少年年龄的LMS诊断更为独特。外阴LMS很容易被误诊为良性阴道病变,导致延迟适当的治疗和较差的结果。在这种情况下,我们介绍了一名14岁的女性，她被诊断为2级外阴LMS，临床上模仿了Bartholin腺囊肿。
