腹膜后胚胎型横纹肌肉瘤1例并文献复习
Retroperitoneal Embryonal Rhabdomyosarcoma: A Case Report and Literature Review
摘要: 腹膜后胚胎型横纹肌肉瘤(eRMS)临床罕见,易侵犯周围血管。本文报道了1例10岁儿童因腹膜后eRMS包绕髂内动脉的病例,影像学检查显示腹膜后巨大混杂密度肿块,增强后边缘强化、中央坏死,数字减影血管造影(DSA)证实肿瘤血供丰富。通过术前行超选择性动脉栓塞减少术中出血,最终成功实施肿瘤切除术的一例诊疗过程。
Abstract: Retroperitoneal embryonal rhabdomyosarcoma (eRMS) is clinically rare and prone to invading surrounding vessels. This paper reports a case of a 10-year-old child with retroperitoneal eRMS encircling the internal iliac artery. Imaging revealed a large heterogeneous density mass in the retroperitoneum, demonstrating marginal enhancement and central necrosis after contrast administration. Digital subtraction angiography (DSA) confirmed abundant tumour blood supply. The diagnostic and therapeutic process is detailed, including preoperative superselective arterial embolisation to minimise intraoperative haemorrhage, culminating in successful tumour resection.
文章引用:杨永梅, 罗亮, 许俊锋. 腹膜后胚胎型横纹肌肉瘤1例并文献复习[J]. 临床医学进展, 2026, 16(1): 261-266. https://doi.org/10.12677/acm.2026.161039

参考文献

[1] Agaram, N.P. (2021) Evolving Classification of Rhabdomyosarcoma. Histopathology, 80, 98-108. [Google Scholar] [CrossRef] [PubMed]
[2] Zhang, Y., Huang, W., Li, L., Qiu, Y., Jiao, H., Chen, Z., et al. (2022) Retroperitoneal Alveolar Rhabdomyosarcoma Intruding into Spinal Canal: A Case Report and Literature Review. Frontiers in Medicine, 9, Article 1019964. [Google Scholar] [CrossRef] [PubMed]
[3] Oberlin, O., Rey, A., Lyden, E., Bisogno, G., Stevens, M.C.G., Meyer, W.H., et al. (2008) Prognostic Factors in Metastatic Rhabdomyosarcomas: Results of a Pooled Analysis from United States and European Cooperative Groups. Journal of Clinical Oncology, 26, 2384-2389. [Google Scholar] [CrossRef] [PubMed]
[4] Sbaraglia, M., Bellan, E. and Dei Tos, A.P. (2020) The 2020 WHO Classification of Soft Tissue Tumours: News and Perspectives. Pathologica, 113, 70-84. [Google Scholar] [CrossRef] [PubMed]
[5] Kim, J., Light, N., Subasri, V., Young, E.L., Wegman-Ostrosky, T., Barkauskas, D.A., et al. (2021) Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults with Rhabdomyosarcoma. JCO Precision Oncology, 5, 75-87. [Google Scholar] [CrossRef] [PubMed]
[6] 乔贵锋. 小儿腹盆腔横纹肌肉瘤的CT表现与病理对比研究[J]. 医学影像学杂志, 2016, 26(9): 1722-1725.
[7] de Vries, I.S.A., van Ewijk, R., Adriaansen, L.M.E., Bohte, A.E., Braat, A.J.A.T., Fajardo, R.D., et al. (2023) Imaging in rhabdomyosarcoma: a patient journey. Pediatric Radiology, 53, 788-812. [Google Scholar] [CrossRef] [PubMed]
[8] Dziuba, I., Kurzawa, P., Dopierała, M., Larque, A.B. and Januszkiewicz-Lewandowska, D. (2018) Rhabdomyosarcoma in Children—Current Pathologic and Molecular Classification. Polish Journal of Pathology, 69, 20-32. [Google Scholar] [CrossRef] [PubMed]
[9] 李艳, 颜彪磊, 谭一楠. 膀胱胚胎性横纹肌肉瘤1例[J]. 诊断病理学杂志, 2021, 28(6): 511-512.
[10] Shenoy, A., Alvarez, E., Chi, Y., Li, M., Shern, J.F., Khan, J., et al. (2021) The Prognostic Significance of Anaplasia in Childhood Rhabdomyosarcoma: A Report from the Children's Oncology Group. European Journal of Cancer, 143, 127-133. [Google Scholar] [CrossRef] [PubMed]
[11] 毛海英. 小儿腹盆部横纹肌肉瘤的CT、MRI表现[J]. 中国中西医结合影像学杂志, 2019, 17(3): 290-292.
[12] 石静, 杜隽, 吴伟, 等. 儿童腹部非脏器起源横纹肌肉瘤的临床及影像特征[J]. 中华肿瘤杂志, 2016, 38(11): 845-851.
[13] Ricciardi, E., Plett, H., Sangiorgio, V., Paderno, M., Landoni, F., Aletti, G., et al. (2020) Adult Primary Cervical Rhabdomyosarcomas: A Multicentric Cross-National Case Series. International Journal of Gynecological Cancer, 30, 21-28. [Google Scholar] [CrossRef] [PubMed]