Hannemann Bernard, McKnoulty Matthew, Kothari Alka
Redcliffe Hospital Redcliffe Queensland Australia.
Oceania University of Medicine Apia Samoa.
Australas J Ultrasound Med. 2016 Nov 21;19(4):154-159. doi: 10.1002/ajum.12030. eCollection 2016 Nov.
Primary uterine malignancy masquerading as a benign leiomyoma is a rare yet devastating condition if missed on ultrasound. Although there are no current guidelines to aide in early ultrasound identification of these high-risk patients prior to histological analysis, certain imaging characteristics may heighten the suspicion of malignancy. Unfortunately, these atypical features are often not included in ultrasonographic reports resulting in delayed treatment and catastrophic consequences. We present a case of a uterine Ewing's sarcoma (ES), which was diagnosed as a multi-fibroid uterus on initial ultrasound. The lack of clinical suspicion resulted in a delay to definitive diagnosis and a sub-optimal surgical resection. We compare this to a standard case of a multi-fibroid uterus in order to highlight the differences in ultrasonographic appearance. This case delineates the importance of accurate identification and open reporting of suspicious features in order to assist ultrasonographers and specialist gynaecologists in creating a differential diagnosis of an otherwise common condition. A high index of suspicion of atypical lesions may lead to early life-saving interventions and careful tissue control during surgery, resulting in improved patient outcomes.
伪装成良性平滑肌瘤的原发性子宫恶性肿瘤是一种罕见但如果在超声检查中漏诊则会造成严重后果的疾病。尽管目前尚无在组织学分析之前辅助超声早期识别这些高危患者的指南,但某些影像学特征可能会增加对恶性肿瘤的怀疑。不幸的是,这些非典型特征通常不包括在超声报告中,从而导致治疗延迟和灾难性后果。我们报告一例子宫尤文肉瘤(ES)病例,该病例最初超声诊断为多发子宫肌瘤。由于缺乏临床怀疑,导致确诊延迟和手术切除不理想。我们将此与多发子宫肌瘤的标准病例进行比较,以突出超声表现的差异。该病例阐明了准确识别和公开报告可疑特征的重要性,以帮助超声检查人员和妇科专家对这种原本常见的疾病进行鉴别诊断。对非典型病变高度怀疑可能会导致早期挽救生命的干预措施,并在手术期间仔细控制组织,从而改善患者的预后。