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首页> 外文期刊>African journal of urology >Malignant peripheral nerve sheath tumour in an unusual location of the urinary bladder: case report and review of literature
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Malignant peripheral nerve sheath tumour in an unusual location of the urinary bladder: case report and review of literature

机译:恶性周围神经鞘瘤在膀胱的一个不寻常的位置:案例报告和文学审查

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Background:Malignant peripheral nerve sheath tumour (MPNST) is a rare malignant soft tissue neoplasm of ectomesenchymal origin. They usually arise from a major or minor peripheral nerve branch or its sheath and also from somatic soft tissues. The most common sites of origin include the extremities and trunk but can sometimes arise an unusual site resulting in the demise of the patient before any intervention.Case presentationWe report a case of 58-year-old male who presented with complaints of weight loss of a year duration, abdominal swelling of 10?months duration and easy fatigability of 3?weeks duration. Digital rectal examination revealed a huge firm mass 6?cm from the anal verge which was non-tender. Abdomino-pelvic ultrasound scan revealed an irregular heterogeneous mass in the posterior wall of the urinary bladder measuring 15.1cmx 14.0?cm with bilateral dilatation of the renal pelvi-calyceal system and ureters. His clinical condition continued to deteriorate while on hospital admission, and he died on the12th day of admission. Post-mortem examination showed a rough ovoid tumour mass firmly adherent to the posterior wall of the bladder with compression of both ureters. Histological and immunohistochemical analysis of the tumour revealed the diagnosis of a MPNST. The final anatomical diagnosis and cause of death was that of a malignant peripheral nerve sheath tumour of the urinary bladder with obstructive uropathy and severe sepsis.ConclusionMPNST can arise at unusual sites other than its common location in the extremities and the existence of neurofibromatosis may not be present. High index of suspicion of MPNST should be raised in rapidly growing painless tumour in and around a nerve tissue. Prompt radio-imaging with biopsy and expert immunohistochemical analysis of lesions will lead to early diagnosis and intervention. Molecular targeted therapies following surgery for MPNST should be developed to improve prognosis and patient outcomes.
机译:背景:恶性周围神经鞘瘤(MPNST)是突出的外胚层源性的罕见恶性软组织肿瘤。它们通常由主要或次要周围神经分支或其护套以及来自躯体软组织的鞘。最常见的原产地包括四肢和树干,但有时可能出现一个不寻常的网站,导致患者在任何干预之前患有患者的消亡.Case呈现我们报告了一个58岁男性的案件,其中包含了减肥投诉的诉讼年龄持续时间,腹部肿胀10?几个月的持续时间,易疲劳为3?持续时间。数字直肠检查显示出巨大的牢固质量6?厘米来自肛门边缘,这是非招标的。腹部 - 盆腔超声扫描显示膀胱后壁中的不规则异质物质,测量为15.1cmx14.0Ωcm,具有双侧扩张肾盂 - 肺炎(肾盂系统和输尿管)。在医院入学期间,他的临床状况继续恶化,他在第12天入院时死亡。验尸后检查显示粗糙的卵形肿瘤质量牢固地粘附在膀胱后壁的压缩中,用两种输尿管压缩。肿瘤的组织学和免疫组织化学分析显示了MPNST的诊断。死亡的最终解剖学诊断和死因是具有阻塞性尿泻和严重败血症的膀胱恶性周围神经鞘瘤的恶性周围神经鞘肿瘤。在四肢常见位置的不寻常场地中可以出现,并且神经纤维瘤病的存在可能不是展示。应在神经组织周围和周围的快速生长无痛的肿瘤中提高MPNST的高度索引。提示与活组织检查和专家免疫组织化学分析病变的迅速映像将导致早期诊断和干预。应开发MPNST手术后的分子靶向疗法,以改善预后和患者结果。

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