Weber Matthieu D, Carlstrom Lucas P, Vignolles-Jeong Joshua, Finger Guilherme, Dhaliwal Joravar, Kobalka Peter J, VanKoevering Kyle K, Prevedello Daniel M, Wu Kyle C
The Ohio State University College of Medicine, Columbus, Ohio.
Departments of Neurological Surgery, The Ohio State University, Columbus, Ohio.
J Neurosurg Case Lessons. 2024 Sep 9;8(11). doi: 10.3171/CASE2435.
Leiomyosarcoma (LMS) is a rare neoplasm that arises from tissues of embryonic mesodermal origin. Primary tissues of origin can include smooth muscle cells of the abdominopelvic viscera, blood vessels, or arrector pili muscles. LMS is known to metastasize to the lungs, with few reported cases of spread to the central nervous system.
A 66-year-old male with cutaneous LMS of the left forearm with metastases to the lungs and kidney that had been treated with chemoradiation presented with worsening headaches. Magnetic resonance imaging revealed a sellar lesion. An endocrine workup was unremarkable. Imaging over 6 months revealed rapid interval growth. Positron emission tomography demonstrated moderate uptake. Given the rapid growth, the patient was offered an endoscopic endonasal approach for resection. Pathology confirmed LMS.
To the authors' knowledge, this is the first documented case of LMS metastasis to the sella. Pituitary carcinoma or metastases to the sellar region should be in the differential among patients with sellar region tumors with a rapid growth rate, bony erosion, or findings of lesions in the upper cervical lymph nodes or soft tissue. Tumors that show significant interval growth should raise suspicion for nonadenomatous lesions, and surgical intervention should be considered even in the absence of endocrinological dysfunction or cranial neuropathies. https://thejns.org/doi/10.3171/CASE2435.
平滑肌肉瘤(LMS)是一种罕见的肿瘤,起源于胚胎中胚层组织。原发组织来源可包括腹盆腔脏器、血管或立毛肌的平滑肌细胞。已知LMS可转移至肺部,很少有转移至中枢神经系统的报道病例。
一名66岁男性,左前臂皮肤LMS伴肺和肾转移,曾接受放化疗,现出现头痛加重。磁共振成像显示鞍区有病变。内分泌检查无异常。6个月的影像学检查显示病变迅速进展。正电子发射断层扫描显示有中度摄取。鉴于病变生长迅速,为患者采用经鼻内镜入路进行切除。病理证实为LMS。
据作者所知,这是首例记录在案的LMS转移至鞍区的病例。垂体癌或鞍区转移应列入鞍区肿瘤患者的鉴别诊断,这些患者具有生长迅速、骨质侵蚀或上颈部淋巴结或软组织有病变表现。病变有显著进展的肿瘤应怀疑为非腺瘤性病变,即使没有内分泌功能障碍或颅神经病变,也应考虑手术干预。https://thejns.org/doi/10.3171/CASE2435