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藏毛性慢性疾病相关的鳞状细胞癌。一种新的治疗方法。

Squamous cell carcinoma over pilonidal chronic disease. A new therapeutic approach.

作者信息

Mayol Oltra A, Boldó Roda E, Lozoya Albacar R, Morillo Macias V, Nobleja Quiles N

机构信息

Department of Surgery, Consorcio Hospitalario Provincial of Castellón, Spain.

Department of Surgery, Consorcio Hospitalario Provincial of Castellón, Spain.

出版信息

Int J Surg Case Rep. 2020;70:172-177. doi: 10.1016/j.ijscr.2020.04.043. Epub 2020 May 11.

Abstract

INTRODUCTION

Pilonidal sinus is a very common disease. Malignant transformation occurs in 0,1% of patients. We present a case of squamous cell carcinoma arised from recurrent pilonidal disease, managed by multimodal treatment.

PRESENTATION OF CASE

We present a 70-year-old man with chronic pilonidal sinus. Inflammation had worsened in previous months and exploration revealed a large ulcerative mass which biopsy showed a squamous cell carcinoma. CT scan and MRI imaging showed tumoral invasion of the coccyx and both gluteus major muscles. Neoadjuvant radiotherapy, chemotherapy as radiosensitizer and surgery with intraoperative radiotherapy was decided in the multidisciplinary tumor committee. Post neoadjuvant therapy MRI showed partial response with a decrease of the mass but persistence of the coccyx infiltration. Surgery consisted in en-bloc resection of the tumor with presacral tissues, coccyx and partial gluteal resection. Intraoperative radiotherapy was administered over the sacrum and in the bed of the coccyx resection. One week later, reconstructive surgery was practiced using a latissimus dorsi free flap, advancement of gluteal flaps and skin graft. Histological examination showed no residual tumor. The patient is currently asymptomatic and he has a satisfactory quality of life.

DISCUSSION

Although squamous cell carcinoma is rare, it must be suspected in patients with recurrent pilonidal disease. Diagnosis is done by histological examination of biopsies. This type of tumors have a high local recurrence rate.

CONCLUSION

We propose a multimodal treatment that includes neoadjuvant radiotherapy and chemotherapy as radiosensitizer and surgery plus intraoperative radiotherapy with the aim to decrease local recurrence rate.

摘要

引言

藏毛窦是一种非常常见的疾病。0.1%的患者会发生恶变。我们报告一例由复发性藏毛疾病引发的鳞状细胞癌病例,采用多模式治疗。

病例介绍

我们报告一名70岁患有慢性藏毛窦的男性。前几个月炎症加重,检查发现一个大的溃疡性肿块,活检显示为鳞状细胞癌。CT扫描和MRI成像显示肿瘤侵犯尾骨和双侧臀大肌。多学科肿瘤委员会决定采用新辅助放疗、作为放射增敏剂的化疗以及术中放疗的手术方式。新辅助治疗后MRI显示部分缓解,肿块缩小但尾骨浸润持续存在。手术包括整块切除肿瘤及骶前组织、尾骨和部分臀肌。术中对骶骨和尾骨切除部位进行放疗。一周后,采用背阔肌游离皮瓣、臀瓣推进和植皮进行重建手术。组织学检查显示无残留肿瘤。患者目前无症状,生活质量良好。

讨论

虽然鳞状细胞癌很少见,但复发性藏毛疾病患者必须怀疑有这种情况。通过活检的组织学检查进行诊断。这类肿瘤局部复发率很高。

结论

我们提出一种多模式治疗方法,包括新辅助放疗和作为放射增敏剂的化疗以及手术加术中放疗,目的是降低局部复发率。

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