A rare case of extra adrenal retroperitoneal paraganglioma: case report

Sakshi Ramnani, Subhash Chawla, M. S. Utaal, Mrigendra Singh, Dakshita Adlakha, Mrugen Thakor
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Abstract

Extra adrenal retroperitoneal paragangliomas are neuro endocrine neoplasms with extremely rare incidence and a wide plethora of clinical presentations. They originate from the neural crest cells interspersed throughout the body. They can present with vague symptoms of pain abdomen, hypertension, palpitations and in severe cases with renal failure, and shock owing to catecholamine excess. On the other end of the spectrum they can be totally asymptomatic and detected incidentally. The multitude of clinical presentations and lack of specific diagnostic tests hence pose a great difficulty in the pre-operative diagnosis of the disease. We are presenting a case of a 20-year-old female with vague symptoms to highlight the management and clinical diagnosis of extra adrenal retroperitoneal paraganglioma.  
肾上腺外腹膜后副神经节瘤:罕见病例报告
肾上腺后腹膜外副神经节瘤是一种神经内分泌肿瘤,发病率极低,临床表现多种多样。它们起源于遍布全身的神经嵴细胞。它们可表现为腹部疼痛、高血压、心悸等模糊症状,严重者可因儿茶酚胺过多而导致肾功能衰竭和休克。另一方面,它们也可能完全没有症状,只是偶然被发现。由于临床表现多种多样,且缺乏特异性诊断测试,因此给该病的术前诊断带来了很大困难。我们将介绍一例症状模糊的 20 岁女性病例,以强调肾上腺外腹膜后副神经节瘤的处理和临床诊断。
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