Benjamin Ramsis, Zhai Jing, Morgan Robert, Prakash Neal
Department of Neurology, City of Hope, Duarte, California, USA.
Department of Pathology, City of Hope, Duarte, California, USA.
BMJ Case Rep. 2014 May 16;2014:bcr2013203361. doi: 10.1136/bcr-2013-203361.
A 22-year-old woman first presented in 2009 with abdominal distention. The diagnosis of stage IA right ovarian tumour was made by fertility-sparing surgery. In the subsequent years, the involvement of the left ovary and metastasis to the lungs prompted further surgical intervention and chemotherapy. By 2013, she experienced insidious, debilitating and diffuse musculoskeletal pain with trismus. Polymyositis or diffuse radiculitis was suspected. Imaging studies identified enhancing lesions in the thigh musculature, temporalis, parotid gland, pterygoid, masseter, tongue, cerebellum and leptomeninges. Biopsy of one of the thigh lesions confirmed the diagnosis of mucinous adenocarcinoma. She succumbed to the disease in November 2013. This case illustrates the aggressive nature of mucinous epithelial ovarian cancer and its resilience to conventional chemotherapy. On account of its high death rate, it is recommended that the epithelial-mesenchymal transition be researched and early therapy targeted at the k-ras oncogene initiated in spite of the tumour's lower initial staging.
一名22岁女性于2009年首次因腹胀就诊。通过保留生育功能的手术诊断为IA期右卵巢肿瘤。在随后的几年里,左卵巢受累及肺部转移促使进一步的手术干预和化疗。到2013年,她出现隐匿性、使人衰弱的弥漫性肌肉骨骼疼痛并伴有牙关紧闭。怀疑为多发性肌炎或弥漫性神经根炎。影像学研究发现大腿肌肉组织、颞肌、腮腺、翼状肌、咬肌、舌、小脑和软脑膜有强化病变。对其中一个大腿病变进行活检确诊为黏液腺癌。她于2013年11月死于该疾病。本病例说明了黏液性上皮性卵巢癌的侵袭性及其对传统化疗的抵抗力。鉴于其高死亡率,建议对上皮-间质转化进行研究,并尽管肿瘤初始分期较低,仍启动针对k-ras癌基因的早期治疗。