Liu Shuzhong, Song An, Zhou Xi, Kong Xiangyi, Li William A, Wang Yipeng, Liu Yong
Department of Orthopaedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences Department of Endocrinology, Key Laboratory of Endocrinology, National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College Department of Neurosurgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China Department of Neurosurgery, Wayne State University School of Medicine, Detroit, MI.
Medicine (Baltimore). 2017 Nov;96(44):e8535. doi: 10.1097/MD.0000000000008535.
We present a rare case of malignant pheochromocytoma with thoracic metastases during pregnancy that presented with symptoms of myelopathy and was treated with circumferential decompression, stabilization, and radiation. The management of this unique case is not well documented. The clinical manifestations, imaging results, pathological characteristics, treatment and prognosis of the case were analyzed.
A 26-year-old pregnant woman with a history of paroxysmal hypertension during the second trimester presented with lower extremity weakness, numbness, urinary incontinence, and back pain. Imaging studies revealed a right adrenal pheochromocytoma, multiple metastases at T8, T11, T12, and the pelvis girdle causing significant multilevel cord compression and significant osteolytic lesions at T11 and T12.
We believe this is the first reported case of metastatic pheochromocytoma of the thoracic spine presenting with symptoms of myelopathy during pregnancy.
A healthy neonate was delivered by emergency caesarean section at 34 weeks. Subsequently, the patient underwent a circumferential spinal cord decompression and a stabilization procedure.
The patient's neurological deficits improved significantly after the surgery, and the postoperative period was uneventful at the 6-month follow-up visit.
This article emphasizes that metastatic pheochromocytoma of the spine, although rare, should be part of the differential when a patient presents with elevated blood pressure, weakness, and urinary incontinence.
我们报告了一例罕见的妊娠期间发生胸段转移的恶性嗜铬细胞瘤病例,该病例表现为脊髓病症状,并接受了环形减压、固定和放疗治疗。该独特病例的治疗方法尚无充分记录。对该病例的临床表现、影像学结果、病理特征、治疗及预后进行了分析。
一名26岁的孕妇,孕中期有阵发性高血压病史,出现下肢无力、麻木、尿失禁和背痛。影像学检查显示右肾上腺嗜铬细胞瘤,T8、T11、T12及骨盆带多发转移,导致严重的多节段脊髓受压,T11和T12有明显的溶骨性病变。
我们认为这是首例妊娠期间出现脊髓病症状的胸椎转移性嗜铬细胞瘤报告病例。
在34周时通过紧急剖宫产分娩出一名健康新生儿。随后,患者接受了环形脊髓减压和固定手术。
术后患者的神经功能缺损明显改善,术后6个月随访期间情况良好。
本文强调,脊柱转移性嗜铬细胞瘤虽然罕见,但当患者出现血压升高、无力和尿失禁时,应作为鉴别诊断的一部分。