Rizzo Alessandro, Nigro Maria Concetta, Ramponi Vania, Gallo Carmine, Perrone Anna Myriam, De Iaco Pierandrea, Frezza Giovanni, Balestrini Damiano, Di Benedetto Maika, Morbiducci Jarno, Pantaleo Maria Abbondanza, Nannini Margherita
Department of Specialized, Experimental and Diagnostic Medicine, S.Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Department of Neurosurgery, Bellaria Hospital, Azienda USL-IRCCS Institute of Neurological Sciences, Bologna, Italy.
Front Oncol. 2020 Jun 16;10:869. doi: 10.3389/fonc.2020.00869. eCollection 2020.
Uterine leiomyosarcoma (uLMS) is a rare and aggressive malignancy with poor clinical outcomes. Even when localized, uLMS is associated with high rates of local and distant recurrences that are usually fatal. Common sites of recurrence are lung, liver, pelvic lymph nodes, and vertebral and long bones, though atypical patterns of recurrence have been described. Among them, intracranial recurrence appears as a rare finding, almost exceptional in skull and dura. We describe the case of a solitary skull metastasis from uLMS in a 39-year-old woman, which represents the third reported case of skull recurrence in literature. After multidisciplinary discussion, the patient underwent surgery and received adjuvant radiotherapy. After 4 months, she is currently alive, without evidence of extracranial disease. This case highlights the importance of suspecting and recognizing atypical and extremely rare metastasis to this region. We encourage the need for large case series in order to provide further information about cranial recurrences of uLMS taking into account the paucity of data currently available in literature and the frequently unpredictable behavior of this rare and highly lethal disease.
子宫平滑肌肉瘤(uLMS)是一种罕见的侵袭性恶性肿瘤,临床预后较差。即使处于局部阶段,uLMS也伴有较高的局部和远处复发率,通常会导致死亡。复发的常见部位是肺、肝、盆腔淋巴结以及椎骨和长骨,不过也有非典型复发模式的报道。其中,颅内复发较为罕见,在颅骨和硬脑膜中几乎是例外情况。我们报告了一例39岁女性uLMS孤立性颅骨转移的病例,这是文献中第三例报道的颅骨复发病例。经过多学科讨论后,该患者接受了手术并接受了辅助放疗。4个月后,她目前仍存活,没有颅外疾病的迹象。该病例突出了怀疑和识别该区域非典型及极其罕见转移的重要性。鉴于目前文献中可用数据匮乏,以及这种罕见且高度致命疾病的行为常常不可预测,我们鼓励开展大型病例系列研究,以便提供更多关于uLMS颅骨复发的信息。