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表现为巨大腹腔内肿块的恶性腹部副神经节瘤。

Malignant abdominal paraganglioma presenting as a giant intra-peritoneal mass.

作者信息

Moslemi Mohammad Kazem, Abolhasani Maryam, Vafaeimanesh Jamshid

机构信息

Department of Urology, Kamkar Hospital, School of Medicine, Qom University of Medical Sciences, Qom, Iran.

出版信息

Int J Surg Case Rep. 2012;3(11):537-40. doi: 10.1016/j.ijscr.2012.07.007. Epub 2012 Jul 28.

Abstract

INTRODUCTION

Paraganglioma is a malignant tumor that arises from the extra adrenal paraganglionic cells of the sympathetic or parasympathetic systems. Herein, we present a case of abdominal mass of unknown histology that underwent a very difficult surgical mass resection. Its final histologic diagnosis was non-functional paraganglioma that was presented as a huge intra-peritoneal mass.

PRESENTATION OF CASE

The patient was a 55-year-old Iranian lady who referred to our center with a giant abdominal mass. Fine needle aspiration (FNA) biopsy showed undifferentiated carcinoma. After laparotomy for mass resection pathology evaluation revealed; malignant paraganglioma, non-metastatic type. Further post-operative patients evaluations showed that the tumor was sporadic in nature and the subsequent patient's natural history was uneventful.

DISCUSSION

Pathologic evaluations have key roles in the exact diagnosis of abdominal masses with unidentified sources. For the paragangliomas, all of them should be regarded malignant until proved otherwise. However, combined use of biochemical markers, immunohistochemical techniques (IHC), and genetic analysis have key roles in the diagnosis and treatment of paragangliomas. Additionally, surgical removal is the proved curative way of paraganglioma treatment.

CONCLUSION

Asymptomatic intra-peritoneal paraganglioma is very rare, especially its malignant variety. This case emphasizes that full pathologic investigation would reveal the exact nature of idiopathic abdominal masses, especially in the state of absence of typical clinical and para-clinical symptoms.

摘要

引言

副神经节瘤是一种起源于交感或副交感神经系统肾上腺外副神经节细胞的恶性肿瘤。在此,我们报告一例组织学不明的腹部肿块病例,该病例经历了非常困难的手术肿块切除。其最终组织学诊断为非功能性副神经节瘤,表现为巨大的腹腔内肿块。

病例介绍

患者为一名55岁的伊朗女性,因巨大腹部肿块转诊至我们中心。细针穿刺(FNA)活检显示未分化癌。剖腹进行肿块切除术后病理评估显示;恶性副神经节瘤,非转移性类型。进一步的术后患者评估表明,该肿瘤本质上是散发性的,随后患者的自然病程平稳。

讨论

病理评估在准确诊断来源不明的腹部肿块中起着关键作用。对于副神经节瘤,在证明其为良性之前,所有病例均应视为恶性。然而,生化标志物、免疫组织化学技术(IHC)和基因分析的联合应用在副神经节瘤的诊断和治疗中起着关键作用。此外,手术切除是已证实的副神经节瘤治疗的治愈方法。

结论

无症状的腹腔内副神经节瘤非常罕见,尤其是其恶性类型。该病例强调全面的病理检查将揭示特发性腹部肿块的确切性质,特别是在缺乏典型临床和亚临床症状的情况下。

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本文引用的文献

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Paraganglioma: not just an extra-adrenal pheochromocytoma.副神经节瘤:不只是肾上腺外嗜铬细胞瘤。
Langenbecks Arch Surg. 2012 Feb;397(2):247-53. doi: 10.1007/s00423-011-0871-y. Epub 2011 Nov 17.
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Renal cell carcinoma mimicking adrenal tumor.肾细胞癌酷似肾上腺肿瘤。
J Oncol. 2010;2010. doi: 10.1155/2010/987128. Epub 2010 Aug 23.
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Asymptomatic paraganglioma of the posterior mediastinum misdiagnosed until operation.后纵隔无症状副神经节瘤术前误诊
Thorac Cardiovasc Surg. 2010 Aug;58(5):302-4. doi: 10.1055/s-0029-1185874. Epub 2010 Aug 2.
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Asymptomatic pheochromocytoma in the posterior mediastinum.后纵隔无症状性嗜铬细胞瘤。
Acta Chir Belg. 2007 Jul-Aug;107(4):465-7. doi: 10.1080/00015458.2007.11680101.
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