Department of Respiratory Diseases, UHC Zagreb, University of Rijeka School of Medicine, Jordanovac 104, 10000, Zagreb, Croatia.
Department of Oncology, UHC Zagreb, Kišpatićeva 12, 10000, Zagreb, Croatia.
World J Surg Oncol. 2019 Aug 19;17(1):147. doi: 10.1186/s12957-019-1691-8.
Primary sarcoma of the lung is a very rare malignant tumor accounting for less than 0.5% of all lung tumors and presenting diagnostic and treatment challenge. We describe a case of a patient diagnosed with primary lung undifferentiated pleomorphic sarcoma developing subsequent peritoneal and small bowel metastases, which stand for highly unusual disease presentation.
A 57-year-old male presented with extensive partially necrotic tumor in the left upper lobe (LUL) of the lung that involved LUL bronchus and extended to the visceral pleura. There was no evidence of nodal or visceral dissemination. After initial presentation, the patient was admitted to the hospital's pulmonology department for further workup. The most likely diagnosis based on biopsy specimen was poorly differentiated sarcoma. Left pneumonectomy with mediastinal lymph node dissection was performed. The final pathohistological diagnosis (PHD) was undifferentiated pleomorphic sarcoma (UPS). Three months after lung surgery, a follow-up CT scan was done which showed a 60-mm obstructive metastatic intraabdominal lesion with small bowel infiltration and further separate peritoneal deposits. Unfortunately, an urgent surgery had to be performed as the patient developed signs of acute abdomen due to bowel perforation. Only 2 months later, the patient passed away at home.
Treatment options of UPS are based on algorithms used in treatment of extremity lesions with well-established role of surgery. However, the role of perioperative chemotherapy remains equivocal with no strong evidence-based data due to the rarity of the disease. Small bowel is an unexpected metastatic site, but of significant clinical relevance.
原发性肺肉瘤是一种非常罕见的恶性肿瘤,占所有肺部肿瘤的比例不到 0.5%,其诊断和治疗具有挑战性。我们描述了一例患者被诊断为原发性肺未分化多形性肉瘤,随后出现腹膜和小肠转移,这代表了非常不常见的疾病表现。
一名 57 岁男性因左上肺(LUL)广泛部分坏死性肿瘤就诊,该肿瘤累及 LUL 支气管并延伸至内脏胸膜。无淋巴结或内脏扩散的证据。初次就诊后,患者被收入医院的肺病科进行进一步检查。根据活检标本,最可能的诊断是低分化肉瘤。行左全肺切除术并纵隔淋巴结清扫术。最终的病理组织学诊断(PHD)为未分化多形性肉瘤(UPS)。肺手术后 3 个月,进行了随访 CT 扫描,显示有 60mm 大小的阻塞性腹腔转移病变,伴有小肠浸润和进一步的孤立性腹膜沉积。不幸的是,由于肠穿孔,患者出现了急性腹痛的症状,必须立即进行紧急手术。仅仅 2 个月后,患者在家中去世。
UPS 的治疗选择基于用于治疗肢体病变的算法,而手术在其中起着重要作用。然而,由于疾病的罕见性,围手术期化疗的作用仍存在争议,没有强有力的循证数据支持。小肠是一个意想不到的转移部位,但具有重要的临床意义。