Nakagawa Makoto, Endo Makoto, Susuki Yosuke, Yokoyama Nobuhiko, Maekawa Akira, Nabeshima Akira, Iida Keiichiro, Fujiwara Toshifumi, Setsu Nokitaka, Matsunobu Tomoya, Matsumoto Yoshihiro, Yokoyama Ryohei, Yamada Yuichi, Kohashi Kenichi, Yamamoto Hidetaka, Oda Yoshinao, Iwamoto Yukihide, Nakashima Yasuharu
Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1, Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Department of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyushu University, 3-1-1, Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
J Clin Med. 2022 Apr 6;11(7):2062. doi: 10.3390/jcm11072062.
Periosteal chondrosarcoma is an extremely rare malignant cartilage-forming tumour that originates from the periosteum and occurs on the surface of bone. Often, it is difficult to distinguish periosteal chondrosarcoma from other tumours, and reports in the literature are scarce. This study aims to investigate the characteristics of periosteal chondrosarcoma, focusing particularly on medullary invasion. Among 33 periosteal cartilaginous tumours, seven patients with pathologically proven periosteal chondrosarcoma were identified retrospectively. The average tumour size was 5.4 cm in the long axis; two tumours were smaller than 3.0 cm. Six tumours were resected with a wide margin, and the remaining tumour had a marginal margin. Histology revealed that six tumours (85.7%) had invaded the medullary cavity; three of these did not show invasion into the medullary cavity on MRI evaluation. Neither local recurrence nor metastasis was observed among these patients. The frequency of invasion of the medullary cavity was higher than that reported previously. The recommended treatment for periosteal chondrosarcoma is resection with an adequate margin. Therefore, surgeons should consider the possibility of medullary invasion when attempting to achieve a histologically negative margin, even if the tumour does not show invasion into the medullary cavity on MRI.
骨膜软骨肉瘤是一种极其罕见的恶性软骨形成肿瘤,起源于骨膜,发生于骨表面。通常,骨膜软骨肉瘤很难与其他肿瘤区分开来,且文献报道稀少。本研究旨在探讨骨膜软骨肉瘤的特征,尤其关注髓腔侵犯情况。在33例骨膜软骨性肿瘤中,回顾性确定了7例经病理证实的骨膜软骨肉瘤患者。肿瘤长轴平均大小为5.4 cm;2个肿瘤小于3.0 cm。6个肿瘤行广泛切除,其余肿瘤行边缘切除。组织学检查显示,6个肿瘤(85.7%)侵犯了髓腔;其中3个在MRI评估中未显示侵犯髓腔。这些患者均未观察到局部复发或转移。髓腔侵犯的频率高于先前报道。骨膜软骨肉瘤的推荐治疗方法是行足够切缘的切除。因此,外科医生在试图获得组织学阴性切缘时,即使肿瘤在MRI上未显示侵犯髓腔,也应考虑髓腔侵犯的可能性。