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[坐骨直肠窝脂肪肉瘤,一个不寻常的肿瘤部位]

[Liposarcoma of the ischiorectal fossa, an unusual tumoral site].

作者信息

Long Pretz P, Detry R, Kestens P J, Haot J

机构信息

Centre de Coloproctologie UCL, Bruxelles.

出版信息

Acta Chir Belg. 1988 May-Jun;88(3):151-4.

PMID:3176792
Abstract

The main locations of the liposarcoma, the most common of the soft tissue sarcomas, are the lower limbs and the retroperitoneal space. We report the case of a 58 year-old male patient presenting with a huge and painless mass of the left fossa ischiorectalis. Preoperative tests and CT-scan of the pelvis evoked the diagnosis of liposarcoma, laminating and lifting the rectum and bladder. Visceral walls were respected. The patient underwent a en-bloc excision of the tumour by a combined perineal and abdominal route. Pathological examination of the mass (1.7 kg) confirmed the diagnosis of well differentiated liposarcoma. No further treatment was initiated, but, because of the high risk of local recurrence, the patient has been placed under a close follow-up schedule.

摘要

脂肪肉瘤是最常见的软组织肉瘤,其主要发病部位是下肢和腹膜后间隙。我们报告一例58岁男性患者,其左坐骨直肠窝出现一个巨大且无痛性肿块。术前检查及骨盆CT扫描提示脂肪肉瘤的诊断,肿瘤包绕并抬高直肠和膀胱,未侵犯脏层壁。患者通过会阴联合腹部途径接受了肿瘤整块切除。对该1.7千克肿块的病理检查确诊为高分化脂肪肉瘤。未进行进一步治疗,但由于局部复发风险高,患者已被安排密切随访。

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1
[Liposarcoma of the ischiorectal fossa, an unusual tumoral site].[坐骨直肠窝脂肪肉瘤,一个不寻常的肿瘤部位]
Acta Chir Belg. 1988 May-Jun;88(3):151-4.
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[A case of retroperitoneal liposarcoma].[一例腹膜后脂肪肉瘤]
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引用本文的文献

1
Leiomyosarcoma of the ischiorectal fossa: report of a novel sphincter and sciatic nerve sparing simultaneous trans-abdominal and trans-gluteal resection and review of the literature.坐骨直肠窝平滑肌肉瘤:一例保留括约肌和坐骨神经的经腹及经臀联合切除术新病例报告并文献复习
J Surg Case Rep. 2015 Mar 10;2015(3):rjv016. doi: 10.1093/jscr/rjv016.
2
Large liposarcoma developing in the ischiorectal fossa: Report of a rare case.发生于坐骨直肠窝的巨大脂肪肉瘤:1例罕见病例报告。
Int J Surg Case Rep. 2013;4(1):51-3. doi: 10.1016/j.ijscr.2012.09.011. Epub 2012 Oct 11.
3
Unusual presentation of a dermoid cyst in the ischiorectal fossa. Magnetic resonance imaging and ultrasound appearances.
坐骨直肠窝皮样囊肿的罕见表现。磁共振成像和超声表现。
Skeletal Radiol. 2009 Sep;38(9):921-4. doi: 10.1007/s00256-009-0705-y. Epub 2009 May 9.