Barbato Giuseppe, Tarantini Alessandro, Serra Francesco, Cabry Francesca, Farinetti Alberto, Sorrentino Lorena, Mattioli Anna Vittoria, Gelmini Roberta
Department of Surgery, University of Modena and Reggio Emilia - Policlinico of Modena, Via del Pozzo, 71 41100, Modena, Italy.
Int J Surg Case Rep. 2019;59:213-216. doi: 10.1016/j.ijscr.2019.05.027. Epub 2019 May 22.
Histiocytic sarcoma (HS) is a very rare malignant histiocytic derivation cancer. The extranodal multisystemic HS has an aggressive clinical course and poor Disease-Free Survival (DFS) and Overall Survival (OS). There are no shared and effective therapeutic protocols; our approach aims to improve the prognosis for advanced diseases.
53-year-old female patient admitted to hospital for intestinal obstruction in April 2016 with evidence of an ileal mass in the right iliac fossa and peritoneal metastases, undergoing urgent surgery of ileal resection, ileostomy and nodular peritoneal mass biopsy. Histological examination diagnosed HS. Staging exams excluded the involvement of other gastro-intestinal districts in the absence of concomitant lymphoproliferative disorders, and PET-CT revealed multiple abdominal and mediastinal nodes hyperplasia. The patient performed chemotherapy and, seeing the partial abdominal extranodal response, was performed cytoreductive surgery (CRS). Histological examination confirmed the diagnosis of HS with multiple peritoneal, ileal, colic and omental localisation. Adjuvant second-line chemotherapy treatment (4 DHAP cycles) was performed. Disease Free Survival at ten months from cytoreductive surgery, Overall Survival at 21 months from diagnosis.
Despite a multimodal therapy with surgery and chemotherapy, extranodal multisystemic HS has a poor prognosis. Up to now the role of surgery is limited to biopsies or complications treatment. Our results of DFS and OS show that cytoreductive surgery may be a valid therapeutic choice.
The surgical approach with major cytoreductive purposes could improve the prognosis in cases with prevalent abdominal extranodal localisation.
组织细胞肉瘤(HS)是一种极为罕见的源自恶性组织细胞的癌症。结外多系统HS具有侵袭性的临床病程,无病生存期(DFS)和总生存期(OS)较差。目前尚无通用且有效的治疗方案;我们的治疗方法旨在改善晚期疾病的预后。
一名53岁女性患者于2016年4月因肠梗阻入院,右髂窝有回肠肿块及腹膜转移的证据,接受了紧急回肠切除术、回肠造口术及结节性腹膜肿块活检。组织学检查确诊为HS。分期检查排除了其他胃肠道区域受累且无伴随的淋巴增殖性疾病,正电子发射断层扫描-计算机断层扫描(PET-CT)显示腹部和纵隔多个淋巴结增生。患者接受了化疗,鉴于腹部结外部分缓解,进行了细胞减灭术(CRS)。组织学检查证实HS诊断,病变位于腹膜、回肠、结肠和网膜多处。进行了辅助二线化疗(4个DHAP周期)。细胞减灭术后10个月无病生存,诊断后21个月总生存。
尽管采用了手术和化疗的多模式治疗,结外多系统HS的预后仍较差。迄今为止,手术的作用仅限于活检或并发症治疗。我们的DFS和OS结果表明,细胞减灭术可能是一种有效的治疗选择。
以主要细胞减灭为目的的手术方法可改善以腹部结外病变为主的病例的预后。