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Primary desmoplastic small round cell tumor of the tibia: PET/CT and MRI presentation of a rare case and review of the literature

机译:胫骨原发性增生性小圆形细胞肿瘤:罕见病例的PET / CT和MRI表现并文献复习

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摘要

Desmoplastic small round cell tumor (DSRCT) was a soft tissue sarcoma of mesenchymal cell origin that typically exhibited a multi-phenotypic pattern of immunohistochemical staining. DSRCT mainly presented in the abdomen sites and primary occurrence in bone was exceptional. In this study, we reported a new case of primary DSRCT of the tibia in a 33-year-old man who had intermittent pain in the left tibia. Radiographs showed transparent lesions in the left upper tibial. MRI revealed a lobular, lytic and ill-identified lesion with adjacent soft tissues swelling of the upper left tibia. CT confirmed notable destruction and wormlike osteolysis of the bone cortex. PET/CT showed a mass of high uptakes, indicating the malignance. He accepted surgical resection with followed multi-agent chemotherapy, containing vincristine, doxorubicin, ifosfamide and etoposide. Clinically and radiologically, the patient did not show any evidence of recurrence or metastasis at 30 months after surgical treatment. Primary osteogenic DSRCT was extremely rare and should be considered in differential diagnosis of bone tumors.
机译:增生性小圆形细胞瘤(DSRCT)是间充质细胞起源的软组织肉瘤,通常表现出免疫组织化学染色的多表型模式。 DSRCT主要表现在腹部部位,主要发生在骨骼中。在这项研究中,我们报道了一名33岁的男性左胫骨间歇性疼痛的胫骨原发性DSRCT的新病例。 X线片显示左上胫骨透明病变。 MRI显示小叶,溶解性和不明确的病变,左上胫骨相邻软组织肿胀。 CT证实骨皮质有明显的破坏和蠕虫状的骨溶解。 PET / CT显示大量摄取,表明恶性。他接受了外科手术切除,随后接受了含有长春新碱,阿霉素,异环磷酰胺和依托泊苷的多药化疗。在临床和放射学上,患者在手术治疗后30个月未显示任何复发或转移的迹象。原发性成骨DSRCT极为罕见,应在骨肿瘤的鉴别诊断中考虑。

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