Ohsawa Manato, Mikuriya Yoshihiro, Ohta Koji, Tanada Minoru, Yamamoto Noriaki, Teramoto Norihiro, Kiyono Masahiro, Sugihara Shinsuke
Department of Surgery, National Hospital Organization Shikoku Cancer Center, 160 Minamiumemotomachikou, Matsuyama-shi, Ehime, Japan.
Department of Surgery, National Hospital Organization Shikoku Cancer Center, 160 Minamiumemotomachikou, Matsuyama-shi, Ehime, Japan.
Int J Surg Case Rep. 2020;68:140-144. doi: 10.1016/j.ijscr.2020.02.041. Epub 2020 Feb 21.
Undifferentiated pleomorphic sarcoma (UPS) is a reclassification of malignant fibrous histiocytoma by the World Health Organization in 2002. UPS, the most common soft tissue sarcoma reported in adults, mostly recurs as lung disease. Pancreatic metastasis of UPS is extremely rare. We present a rare case of pelvic UPS with pancreatic metastasis.
A 69-year-old man was identified as having mediastinal lymphadenopathy on follow-up computed tomography (CT), 2 years after undergoing surgery for gastric adenocarcinoma (pT4aN3M0/IIIC). Subsequent positron emission tomography-CT (PET/CT) indicated pelvic lesions and magnetic resonance imaging (MRI) showed multiple tumors of the left pubis and femur. Histopathology of diagnostic thoracoscopic lymph node dissection and CT-guided needle biopsy of the left pubic lesion showed UPS. Systemic chemotherapy and targeted molecular therapy reduced multiple pelvic and metastatic tumors. Left pubic primary lesion contraction was achieved with intensity-modulated radiation therapy. CT performed 4 years after treatment initiation showed a 40-mm pancreatic head mass. Lesions other than the pancreatic tumor were in remission, and a pancreatoduodenectomy was performed. Histological analysis confirmed pancreatic metastasis of anaplastic pleomorphic sarcoma.
Reports of pelvic UPS with pancreatic metastasis, as that of the present case, are extremely rare. UPS is malignant potential tumor, and complete excision is the first treatment option, while the usefulness of chemotherapy or radiation therapy remains uncertain.
Complete resection is vital for local control in pancreatic metastasis of UPS. Sites of recurrence are rare; hence, patients must be carefully followed up.
未分化多形性肉瘤(UPS)是2002年世界卫生组织对恶性纤维组织细胞瘤的重新分类。UPS是成人中报告的最常见软组织肉瘤,大多复发为肺部疾病。UPS的胰腺转移极为罕见。我们报告一例罕见的盆腔UPS伴胰腺转移病例。
一名69岁男性在接受胃腺癌手术(pT4aN3M0/IIIC)2年后,随访计算机断层扫描(CT)发现纵隔淋巴结肿大。随后的正电子发射断层扫描-CT(PET/CT)显示盆腔病变,磁共振成像(MRI)显示左耻骨和股骨有多个肿瘤。诊断性胸腔镜淋巴结清扫的组织病理学检查以及左耻骨病变的CT引导下针吸活检显示为UPS。全身化疗和靶向分子治疗使多个盆腔和转移瘤缩小。调强放射治疗使左耻骨原发性病变缩小。治疗开始4年后进行的CT显示胰头有一个40毫米的肿块。胰腺肿瘤以外的病变均缓解,遂行胰十二指肠切除术。组织学分析证实为间变性多形性肉瘤的胰腺转移。
如本病例所示,盆腔UPS伴胰腺转移的报道极为罕见。UPS是具有恶性潜能的肿瘤,完整切除是首选治疗方案,而化疗或放射治疗的有效性仍不确定。
完整切除对于UPS胰腺转移的局部控制至关重要。复发部位罕见;因此,必须对患者进行仔细随访。