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巨大腹膜后陈旧性神经鞘瘤:术前活检是否总是必要的?

Giant retroperitoneal ancient schwannoma: Is preoperative biopsy always mandatory?

作者信息

Al Skaini Mohammad Saad, Haroon Hesham, Sardar Ali, Bazeed Mohammad, Al Zain Abbas, Al Shahrani Mushabab, El Hakeem Howaida, Al Shraim Mubarak, Al Amri Abdul Rahman M, Ezzedien Rabie M

机构信息

Department of Surgery, Armed Forces Hospital, Southern Region, Saudi Arabia.

Department of Radiology, Armed Forces Hospital, Southern Region, Saudi Arabia.

出版信息

Int J Surg Case Rep. 2015;6C:233-6. doi: 10.1016/j.ijscr.2014.08.015. Epub 2014 Dec 11.

Abstract

INTRODUCTION

Schwannoma is the term given to tumours arising from Schwann cells of any nerve sheath. It may arise in the retroperitoneum, where it can attain enormous sizes and cause considerable diagnostic and therapeutic difficulties. A variety of incapacitating symptoms may arise, depending on its size alone and the related contagious organs.

PRESENTATION OF CASE

A 71-year-old female, who was incapacitated by a giant abdominal mass, associated with weight loss, immobility, general weakness and constipation. Radiologically, the presence of a huge pelviabdominal tumour was confirmed. A preoperative tissue diagnosis was entertained but omitted, and we resorted to direct surgical excision instead. During surgery, significant bleeding from the surrounding lumbar vessels was encountered, but it was controlled and the tumour was excised intact. Histopathologically, it showed the histologic features of ancient schwannoma.

DISCUSSION

In the patient presented here, who was rendered immobile by the tumour, total excision or at least debulking seemed appropriate, regardless of any biopsy result.

CONCLUSION

The diagnosis of retroperitoneal schwannoma and its variant "ancient schwannoma" should be considered when a huge pelviabdominal tumour is encountered. Although CT guided biopsy may be helpful in reaching a preoperative diagnosis, this might not change the decision for the need of total tumour excision or at least debulking, in the presence of incapacitating symptoms. With large tumours, the possibility of perioperative exanginating haemorrhage should be remembered and the necessary precautions activated.

摘要

引言

施万细胞瘤是指起源于任何神经鞘雪旺细胞的肿瘤。它可发生于腹膜后,在那里可长得很大,并导致相当大的诊断和治疗困难。根据其大小及相关受累器官的不同,可能会出现各种使人丧失能力的症状。

病例介绍

一名71岁女性,因巨大腹部肿块而行动不便,伴有体重减轻、活动受限、全身虚弱和便秘。影像学检查证实存在巨大的盆腔腹部肿瘤。曾考虑进行术前组织诊断,但未实施,而是直接进行了手术切除。手术过程中,遇到来自周围腰血管的大量出血,但出血得到控制,肿瘤完整切除。组织病理学检查显示为陈旧性施万细胞瘤的组织学特征。

讨论

在此病例中,患者因肿瘤而行动不便,无论活检结果如何,完整切除或至少减瘤似乎都是合适的。

结论

当遇到巨大的盆腔腹部肿瘤时,应考虑腹膜后施万细胞瘤及其变异型“陈旧性施万细胞瘤”的诊断。尽管CT引导下活检可能有助于术前诊断,但在存在使人丧失能力的症状时,这可能不会改变对肿瘤完整切除或至少减瘤必要性的决定。对于巨大肿瘤,应牢记围手术期出血的可能性,并采取必要的预防措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b124/4347965/2e595851ecc7/gr1.jpg

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