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Desmoid abdominal tumour: a clinical case report and brief literature review

机译:腹部恶性肿瘤:一例临床报告并简要文献复习

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Desmoid tumours are unique mesenchymal neoplasm. They are able to spread to proximal tissues but tend not to metastasize. Our case presents a 66-year-old female referred for evaluation of the prominent, palpable mass located into the left abdomen. Imaging studies revealed a tumour up to 22 cm, extending below the diaphragm to the retroperitoneal and intra-abdominal cavity. Contrast enhanced ultrasound showed strong inhomogeneous arterial hyper-enhancement followed by persistent enhancement in a venous phase. Histology obtained with tru-cut needle biopsy established desmoid tumour, with overall proliferating activity (Ki-67 expression) of 20%. The lesion had been identified as sporadic and ‘unresectable’. During the patient’s follow-up a slow but continuous elevation of serum creatinine was registered eventually led to anuria, requiring emergent haemodialysis. The non-obstructing nephropathy is an unusual complication of the disease course, therefore we briefly reviewed the published data on abdominal desmoid tumours and critically analysed the relation with kidney injury.
机译:胶质瘤是独特的间质肿瘤。它们能够扩散到近端组织,但往往不会转移。我们的病例介绍了一位66岁的女性,该女性被评估为位于左腹部的突出,可触及的肿块。影像学检查发现肿瘤长至22 cm,从横diaphragm膜下方延伸至腹膜后腔和腹腔内。超声造影显示强烈的不均匀动脉过度增强,随后在静脉期持续增强。 tru-cut针穿刺活检获得的组织学证实为类胶质瘤,总增殖活性(Ki-67表达)为20%。该病灶被确定为零星的和“无法切除的”。在患者的随访过程中,发现血清肌酐缓慢但持续升高,最终导致无尿,需要紧急血液透析。非阻塞性肾病是该病程的一种罕见并发症,因此我们简要回顾了有关腹部结石性肿瘤的公开数据,并严格分析了其与肾脏损伤的关系。

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