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腹膜后神经鞘瘤的罕见表现:一例病例报告

Rare presentation of retroperitoneal schwannoma: a case report.

作者信息

Mozafar Mohammad, Lotfollahzadeh Saran, Atqiaee Khashayar, Adhamy Farideh

机构信息

Dept. of General and Vascular Surgery, Shahid Beheshti University of Medical Sciences, Tehran, Iran ; Cancer Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Cancer Prev. 2014 Spring;7(2):107-10.

Abstract

The deadly Schwannomas, as uncommon subtype of soft tissue tumors originate from peripheral nerve sheaths. Retro peritoneum is an uncommon site for these tumors. Here we present the clinical feature and therapeutic implication of a 38-year-old man affected by recurrent retroperitoneal schwannoma who admitted to emergency ward following abdominal pain. Computed Tomorgraphic Scan showed a solid well-differentiated heterogeneous mass, 8.5x6 cm size in portahepatis beneath liver and right periumbilical .On laboratory tests Cancer Antigen 19-9 and Cancer Embryonic Antigen were in normal range. In surgery, a 7x8cm round mass was discovered at juxta renal juxta duodenal retro peritoneum, It was completely adhered to second part of duodenum with no signs of infiltration of the liver and right kidney, unable to simply being enucleated, curative resection was performed by classical whipple procedure. The patient`s hospitalization course was uneventful and on the second week he was discharged from the hospital with complete recovery. Due to the high recurrent rate of retroperitoneal Schwannomas even in benign circumstances, radical resection would be the treatment of choice.

摘要

致命性神经鞘瘤是一种罕见的软组织肿瘤亚型,起源于周围神经鞘膜。腹膜后是这些肿瘤的罕见发病部位。在此,我们报告一名38岁男性复发性腹膜后神经鞘瘤的临床特征及治疗意义,该患者因腹痛入住急诊病房。计算机断层扫描显示肝脏下方肝门和右脐周有一个大小为8.5×6 cm的实性、分化良好的异质性肿块。实验室检查显示癌胚抗原19-9和癌胚抗原在正常范围内。手术中,在肾旁十二指肠旁腹膜后发现一个7×8 cm的圆形肿块,它与十二指肠第二部完全粘连,无肝脏和右肾浸润迹象,无法简单摘除,遂通过经典的惠普尔手术进行根治性切除。患者住院过程顺利,第二周出院,完全康复。由于腹膜后神经鞘瘤即使在良性情况下复发率也很高,根治性切除是首选治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef2/4142949/f261264fc916/IJCP-07-107f1.jpg

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