Metastatic lesions of the uterus, fallopian tubes and ovaries in undifferentiated pleomorphic sarcoma of the left tibia (clinical case)

O. I. Kit, E. Verenikina, A. Menshenina, L. Vladimirova, E. Kalabanova, T. Lapteva, A. A. Barashev, K. S. Eremin, A. Ardzha
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Abstract

Undifferentiated pleomorphic osteosarcoma belongs to the group of rarely occurring tumors. Despite the treatment, the disease progresses in 30–40 % of patients with osteosarcomas. The main route of metastasis of bone tissue sarcomas is hematogenous, while lymphogenic spread is observed less frequently. As a rule, secondary metastatic changes occur in the lungs. Less often there is a secondary lesion of the bones of the skeleton and brain. Metastatic lesion of uterus, fallopian tubes and ovaries in malignant undifferentiated pleomorphic sarcoma is extremely rare. Therefore, we found it interesting to describe a clinical case of such a rare metastatic lesion. Patient K. underwent amputation of the left limb at the level of the lower third of the femur for undifferentiated pleomorphic sarcoma of the left tibia in 2019, and 4 courses of adjuvant polychemotherapy were performed. In 20 months after completion of complex treatment of the primary tumor, complaints of lower abdominal pain, increased body temperature up to 37.8 °C in the evenings appeared. According to the results of follow-up examination, a voluminous, multinodular, solid mass of merging character was detected in the pelvis, with total dimensions of up to 11 cm, and a cavitary mass of up to 5 cm was detected in the posterior vault. A trepan-biopsy of the mass in the projection of the right ovary was performed. The morphological picture in the volume of trepan biopsy specimens is characteristic of spindle cell sarcoma. Metastasis of undifferentiated pleomorphic bone sarcoma (malignant fibrous histiocytoma) is most likely. Due to metastatic lesions of the uterus, fallopian tubes, ovaries, omentum, mesentery and serous membrane of the colon loops, peritoneum of the bladder, surgical intervention in the volume of removal of the distal part of the sigmoid colon, rectosigmoid, upper ampullary parts of the rectum, uterus with fallopian tubes and ovaries, appendix was performed. Immunohistochemical study of the postoperative material revealed that the immunophenotype of tumor cells confirmed the morphological picture typical for undifferentiated pleomorphic bone sarcoma. The patient was further prescribed antitumor drug therapy. This clinical case demonstrates a rare, atypical metastasis of undifferentiated pleomorphic osteosarcoma, which allows to expand the knowledge about the flow of malignant diseases of this localization.
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左胫骨未分化多形性肉瘤的子宫、输卵管和卵巢转移病灶(临床病例)
未分化多形性骨肉瘤属于罕见肿瘤。尽管接受了治疗,但 30-40% 的骨肉瘤患者病情仍会发展。骨组织肉瘤的主要转移途径是血行转移,而淋巴转移则较少见。一般来说,继发性转移病变发生在肺部。骨骼和大脑继发病变的情况较少。恶性未分化多形性肉瘤的子宫、输卵管和卵巢转移病变极为罕见。因此,我们认为描述这样一个罕见转移病灶的临床病例很有意义。患者 K 于 2019 年因左侧胫骨未分化多形性肉瘤接受了股骨下 1/3 水平的左侧肢体截肢手术,并进行了 4 个疗程的多化疗辅助治疗。在完成原发肿瘤的综合治疗 20 个月后,出现了下腹痛、晚上体温升高至 37.8 °C。随访检查结果显示,骨盆中发现了一个体积巨大、多结节、实性的合并肿块,总尺寸达 11 厘米,后穹隆中发现了一个 5 厘米的空腔性肿块。对右侧卵巢投影处的肿块进行了穿刺活检。穿刺活检标本体积的形态学特征是纺锤形细胞肉瘤。最有可能是未分化多形性骨肉瘤(恶性纤维组织细胞瘤)的转移。由于子宫、输卵管、卵巢、网膜、结肠襻肠系膜和浆膜、膀胱腹膜发生转移性病变,因此进行了手术干预,切除了乙状结肠远端、直肠乙状结肠、直肠上部ampullary部分、子宫及输卵管和卵巢、阑尾。术后材料的免疫组化研究显示,肿瘤细胞的免疫表型证实了未分化多形性骨肉瘤的典型形态学特征。患者接受了进一步的抗肿瘤药物治疗。该临床病例展示了一种罕见的非典型未分化多形性骨肉瘤转移,有助于扩大对这种局部恶性疾病的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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