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Aggressive angiomyxoma of broad ligament: an uncommon mesenchymal tumor

机译:阔韧带侵袭性血管平滑肌瘤:一种罕见的间质瘤

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Aggressive angiomyxoma is a rare mesenchymal tumor occurring predominantly in the pelviperineal region. Authors present a case of a 70 years female presented with history of distention of lower abdomen with recurrent pain since 6 months. On clinical examination there was suspicion of fibroid. On USG it was reported as huge fleshy, soft tissue mass measuring 20x10x9 cm in lower abdominal flanks and pelvis with vascular pedicle attached to right parametrium. Pan-hysterectomy was performed. Right broad ligament showed mass measuring 18.5x10x6 cm. On histopathological examination it was diagnosed as a case of Aggressive angiomyxoma of broad ligament. We are presenting this case for its extreme rarity, clinicohisto-pathological and radiological findings.
机译:侵袭性血管粘液瘤是一种罕见的间质肿瘤,主要发生在盆腔会阴区。作者介绍了一个病例,该病例为一名70岁女性,自6个月以来一直有小腹胀痛和反复疼痛的病史。在临床检查中,怀疑有肌瘤。在USG上,据报道为下腹部腹侧和骨盆中巨大的肉质软组织,大小为20x10x9 cm,血管蒂附着在右子宫旁侧。进行全子宫切除术。右宽韧带显示质量为18.5x10x6 cm。经组织病理学检查,诊断为宽韧带侵袭性血管平滑肌瘤。我们介绍此病例的原因是其极为罕见,临床组织病理学和放射学发现。

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