Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor: A Case Report and Review of the Literature

被引:4
作者
Rizzo, Alessandro [1 ]
Nigro, Maria Concetta [1 ]
Ramponi, Vania [2 ]
Gallo, Carmine [3 ]
Perrone, Anna Myriam [4 ]
De Iaco, Pierandrea [4 ]
Frezza, Giovanni [5 ]
Balestrini, Damiano [5 ]
Di Benedetto, Maika [6 ]
Morbiducci, Jarno [7 ]
Pantaleo, Maria Abbondanza [1 ,8 ]
Nannini, Margherita [9 ]
机构
[1] Univ Bologna, S Orsola Malpighi Hosp, Dept Specialized Expt & Diagnost Med, Bologna, Italy
[2] Bellaria Hosp, Azienda USL IRCCS Inst Neurol Sci, Dept Neurosurg, Bologna, Italy
[3] Osped Bellaria, Anat Pathol, Bologna, Italy
[4] St Orsola Marcello Malpighi Hosp, Gynecol Oncol Unit, Bologna, Italy
[5] Bellaria Hosp, Dept Radiotherapy, Bologna, Italy
[6] Azienda Osped Univ, Osped Riuniti Ancona, Radiotherapy Unit, Ancona, Italy
[7] Macerata Hosp, ASUR Marche, Zona Terr 9, Macerata, Italy
[8] Univ Bologna, Giorgio Prodi Canc Res Ctr, Bologna, Italy
[9] S Orsola Malpighi Univ Hosp, Med Oncol Unit, Bologna, Italy
关键词
uterine leiomyosarcoma; uterine sarcoma; skull metastasis; uterine cancer; intracranial recurrence; CLINICAL-PRACTICE GUIDELINES; MANAGEMENT; SARCOMA; BRAIN;
D O I
10.3389/fonc.2020.00869
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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