TY - JOUR
T1 - Skull Metastasis From Uterine Leiomyosarcoma, a Rare Presentation for a Rare Tumor
T2 - A Case Report and Review of the Literature
AU - Rizzo, Alessandro
AU - Nigro, Maria Concetta
AU - Ramponi, Vania
AU - Gallo, Carmine
AU - Perrone, Anna Myriam
AU - De Iaco, Pierandrea
AU - Frezza, Giovanni
AU - Balestrini, Damiano
AU - Di Benedetto, Maika
AU - Morbiducci, Jarno
AU - Pantaleo, Maria Abbondanza
AU - Nannini, Margherita
N1 - Publisher Copyright:
© Copyright © 2020 Rizzo, Nigro, Ramponi, Gallo, Perrone, De Iaco, Frezza, Balestrini, Di Benedetto, Morbiducci, Pantaleo and Nannini.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/6/16
Y1 - 2020/6/16
N2 - 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.
AB - 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.
KW - intracranial recurrence
KW - skull metastasis
KW - uterine cancer
KW - uterine leiomyosarcoma
KW - uterine sarcoma
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U2 - 10.3389/fonc.2020.00869
DO - 10.3389/fonc.2020.00869
M3 - Article
AN - SCOPUS:85087294930
VL - 10
JO - Frontiers in Oncology
JF - Frontiers in Oncology
SN - 2234-943X
M1 - 869
ER -