Bonomo Giulio, Gans Alessandro, Mazzapicchi Elio, Rubiu Emanuele, Alimonti Paolo, Eoli Marica, Paterra Rosina, Pollo Bianca, Iess Guglielmo, Restelli Francesco, Falco Jacopo, Acerbi Francesco, Schiariti Marco Paolo, Ferroli Paolo, Broggi Morgan
Department of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
School of Medicine, University of Milan, Milan, Italy.
Front Oncol. 2023 Feb 24;13:1100532. doi: 10.3389/fonc.2023.1100532. eCollection 2023.
Sporadic Spinal Psammomatous Malignant Melanotic Nerve Sheath Tumor (SSP-MMNST) is a rare subgroup of peripheral nerve sheath tumors arising along the spine. Only a few reports of SSP-MMNST have been described. In this paper, we review the literature on SSP-MMNST focusing on clinical, and diagnostic features, as well as investigating possible pathogenetic mechanisms to better implement therapeutic strategies. We also report an illustrative case of a young female presenting with cervicobrachial pain due to two SSP-MMNSTs arising from C5-6 right spinal roots.
We report a case of a 28-year-old woman presenting with right arm weakness and dysesthesia. Clinical examination and neuroimaging were performed, and, following surgical removal of both lesions, a histological diagnosis of SSP-MMNST was obtained.
The literature review identified 21 eligible studies assessing 23 patients with SSP-MMNST, with a mean onset age of 41 years and a slight male gender preference. The lumbar district was the most involved spinal segment. Gross-total resection (GTR) was the treatment of choice in all amenable cases, followed in selected cases with residual tumor by adjuvant radiotherapy or chemotherapy. The metastatic and recurrence rates were 31.58% and 36.8%, respectively.
Differently from common schwannomas, MMNST represents a rare disease with known recurrence and metastatization propensity. As reported in our review, SSP-MMNST has a greater recurrence rate when compared to other forms of spinal MMNST, raising questions about the greater aggressiveness of the former. We also found that residual disease is related to a higher risk of systemic disease spreading. This metastatic potential, usually associated with primary lumbar localization, is characterized by a slight male prevalence. Indeed, whenever GTR is unachievable, considering the higher recurrence rate, adjuvant radiation therapy should be taken into consideration.
散发性脊柱砂粒体性恶性黑色素性神经鞘瘤(SSP - MMNST)是一种沿脊柱发生的周围神经鞘瘤的罕见亚型。关于SSP - MMNST的报道仅有少数几例。在本文中,我们回顾了关于SSP - MMNST的文献,重点关注临床和诊断特征,并研究可能的发病机制,以更好地实施治疗策略。我们还报告了一例年轻女性因C5 - 6右侧脊神经根出现两个SSP - MMNST而表现为颈臂痛的典型病例。
我们报告一例28岁女性,表现为右臂无力和感觉异常。进行了临床检查和神经影像学检查,在手术切除两个病变后,获得了SSP - MMNST的组织学诊断。
文献综述确定了21项符合条件的研究,评估了23例SSP - MMNST患者,平均发病年龄为41岁,男性略占优势。腰椎区是受累最多的脊柱节段。在所有适合的病例中,全切除(GTR)是首选治疗方法,在部分有残留肿瘤的病例中,随后采用辅助放疗或化疗。转移率和复发率分别为31.58%和36.8%。
与常见的神经鞘瘤不同,MMNST是一种已知具有复发和转移倾向的罕见疾病。正如我们综述中所报道的,与其他形式的脊柱MMNST相比,SSP - MMNST的复发率更高,这引发了关于前者更具侵袭性的疑问。我们还发现残留病灶与全身疾病扩散的较高风险相关。这种转移潜能通常与原发性腰椎定位有关,其特征是男性略多。确实,每当无法实现GTR时,考虑到较高的复发率,应考虑辅助放射治疗。