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首页> 外文期刊>BMC Surgery >Haemorrhagic retroperitoneal paraganglioma initially manifesting as acute abdomen: a rare case report and literature review
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Haemorrhagic retroperitoneal paraganglioma initially manifesting as acute abdomen: a rare case report and literature review

机译:出血性腹膜腹膜血管瘤最初表现为急性腹部:罕见的报告和文献综述

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Paragangliomas (PGLs) are extremely rare neuroendocrine tumours arising from extra-adrenal chromaffin cells. PGLs are clinically rare, difficult to diagnose and usually require surgical intervention. PGLs mostly present catecholamine-related symptoms. We report a case of Acute abdomen as the initial manifestation of haemorrhagic retroperitoneal PGL. There has been only one similar case reported in literature. We present a unique case of a 52-year-old female with acute abdomen induced by haemorrhagic retroperitoneal PGL. The patient had a 5-h history of sudden onset of serve right lower quadrant abdominal pain radiating to the right flank and right lumbar region. Patient had classic symptoms of acute abdomen. Abdominal ultrasound revealed a large abdominal mass with a clear boundary. A Computed Tomography Angiography (CTA) of superior mesenteric artery was also performed to in the emergency department. The CTA demonstrated a large retroperitoneal mass measured 9.0?×?7.3?cm with higher density inside. A provisional diagnosis of retroperitoneal tumour with haemorrhage was made. The patient received intravenous fluids, broad-spectrum antibiotics and somatostatin. On the 3rd day of admission, her abdominal pain was slightly relieved, but haemoglobin decreased from 10.9 to 9.4?g/dL in 12?h suggesting that there might be active bleeding in the abdominal cavity. Thus, we performed a midline laparotomy for the patient. Haemorrhage was successfully stopped during operation. The retroperitoneal tumour with haemorrhage was completely removed. The abdominal pain was significantly relieved after surgery. The patient initially presented with acute abdomen instead of catecholamine-related symptoms. The diagnosis of retroperitoneal PGL with haemorrhage was finally confirmed by postoperative pathological and immunohistochemical results. The postoperative course was uneventful. At the 1-year follow-up visit, no tumour recurrence was observed by Single Photon Emission Computed Tomography. A literature review was performed to further understand and analyse the aforementioned disease. Acute abdomen as the initial manifestation of haemorrhagic retroperitoneal paraganglioma is extremely rare. Abdominal Computed Tomography is essential to locate the lesion and differentiate between other causes of acute abdomen. PGLs are hypervascular tumours. We should be aware that ruptured retroperitoneal PGL with massive bleeding could be life threatening and require emergency laparotomy.
机译:Paragangliomas(PGL)是来自肾上腺斑铬细胞产生的极其罕见的神经内分泌肿瘤。 PGL在临床上稀有,难以诊断,通常需要手术干预。 PGLS大多出现了相关的儿茶酚胺相关症状。我们报告了急性腹部的案例作为出血性腹膜术术的初始表现。在文献中只报告了一个类似的案例。我们为一名52岁的女性呈现出一种急性腹部的一个独特的案例,血腥腹膜腹膜术诱导。患者有5-H历史的突然发作的右下象限腹痛辐射到右侧侧腰部疼痛。患者有急性腹部的经典症状。腹部超声显示出具有透明边界的大腹部肿块。还在急诊部门进行了高级肠系膜动脉的计算断层造影血管造影(CTA)。 CTA显示出大的腹膜腹膜质量测量9.0××7.3厘米,内部密度较高。制备了腹膜瘤肿瘤术的临时诊断。患者接受静脉内流体,广谱抗生素和生长抑制菌素。在第3天的入学中,她的腹痛略微松弛,但血红蛋白从10.9〜9.4℃下降,12?H中的G / DL表明腹腔中可能有活性出血。因此,我们对患者进行了中线剖腹术。在运营期间成功停止了出血。完全除去具有出血的腹膜瘤肿瘤。手术后腹痛显着缓解。最初用急性腹部呈现的患者而不是儿茶酚胺相关的症状。通过术后病理和免疫组织化学结果,最终确诊具有出血的腹膜瘤PGL的诊断。术后过程很顺利。在1年的随访期间,单光子发射计算机断层扫描未观察到肿瘤复发。进行文献综述以进一步了解和分析上述疾病。急性腹部作为出血性腹膜腹膜血管瘤的初始表现极少数。腹部计算断层扫描对于定位病变并区分急性腹部的其他原因是必不可少的。 PGL是高血管肿瘤。我们应该意识到破裂的腹膜后腹膜PG1具有巨大出血可能是危及生命,需要紧急剖腹手术。

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