Rapidly enlarging port-site mass after thoracoscopic lung resection: desmoid-type fibromatosis mimicking pleural recurrence.

IF 0.4
Go Kamimura, Masaya Aoki, Tomohiko Matsushita, Satomi Imamura, Shoichiro Morizono, Yuto Nonaka, Aya Takeda, Koki Maeda, Toshiyuki Nagata, Kazuhiro Ueda
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Abstract

Background: Desmoid-type fibromatosis is a rare, benign fibroblastic neoplasm characterized by infiltrative growth and a tendency for local recurrence despite the absence of metastatic potential. It has been associated with prior trauma or surgery, and postoperative lesions arising in the chest wall can present a major diagnostic challenge. In patients after lung cancer resection, a new pleural-based or chest wall mass at a previous port site is often interpreted as pleural dissemination, chest wall recurrence, or port-site implantation, even when the primary tumor is pathologically low risk.

Case presentation: A 70-year-old woman underwent minimally invasive resection for lung adenocarcinoma, and the final pathological stage was pT1miN0M0 (pStage IA1). She remained asymptomatic, and routine postoperative surveillance was performed. At 10 months after surgery, computed tomography revealed a newly developed, well-demarcated soft-tissue mass arising from the chest wall at the thoracoscopic port site, adjacent to the pleura; the mass rapidly enlarged to 3.0 cm by 14 months. Positron emission tomography/computed tomography with fluorine-18 fluorodeoxyglucose showed mild tracer uptake within the lesion (maximum standardized uptake value, 2.5). Although the primary lung adenocarcinoma was pathologically low risk, pleural dissemination or port-site recurrence could not be confidently excluded based on imaging alone. Considering the need for definitive diagnosis and local control, the patient underwent en bloc resection of the lesion with chest wall excision including the seventh rib. Grossly, the tumor was firm and fibrous. Histopathological examination demonstrated a proliferation of bland spindle-shaped cells embedded in abundant collagenous stroma with infiltrative margins, consistent with desmoid-type fibromatosis. The postoperative course was uneventful. As the surgery was performed recently, long-term follow-up data are not yet available.

Conclusions: Desmoid-type fibromatosis can occur at a thoracoscopic port site more than one year after lung cancer surgery and may mimic pleural dissemination or port-site recurrence, even after resection of minimally invasive adenocarcinoma. When malignancy cannot be excluded preoperatively, surgical excision with an adequate margin can establish the diagnosis and achieve local disease control.

胸腔镜肺切除术后快速增大的肺门部位肿块:模拟胸膜复发的硬纤维瘤病。
背景:硬纤维瘤是一种罕见的良性纤维母细胞肿瘤,其特点是浸润性生长和局部复发的倾向,尽管没有转移的潜力。它与先前的创伤或手术有关,胸壁术后病变可能是主要的诊断挑战。在肺癌切除术后的患者中,即使原发肿瘤在病理上是低风险的,在先前的肺脏部位出现新的胸膜或胸壁肿块也常被解释为胸膜播散、胸壁复发或肺脏部位植入。病例介绍:70岁女性肺腺癌行微创切除术,最终病理分期为pT1miN0M0 (pStage IA1)。她仍然无症状,并进行了常规术后监测。手术后10个月,计算机断层扫描显示在胸腔镜下靠近胸膜的胸壁上出现了一个新发展的、界限清晰的软组织肿块;14个月肿物迅速扩大至3.0 cm。正电子发射断层扫描/氟-18氟脱氧葡萄糖计算机断层扫描显示病灶内轻度示踪剂摄取(最大标准化摄取值,2.5)。虽然原发性肺腺癌的病理风险较低,但仅凭影像学检查不能排除胸膜播散或肺门部位复发。考虑到明确诊断和局部控制的需要,患者接受了包括第七肋骨在内的胸壁切除术。肉眼可见,肿瘤坚硬且呈纤维状。组织病理学检查显示淡色纺锤形细胞增生,包埋在丰富的胶原基质中,边缘浸润,与纤维瘤样病变一致。术后过程平淡无奇。由于手术是最近进行的,长期随访数据尚未获得。结论:纤维瘤样病变可发生在肺癌手术后一年多的胸腔镜肺门部位,甚至在微创腺癌切除后也可能发生类似胸膜播散或肺门部位复发。当术前不能排除恶性肿瘤时,手术切除适当的切缘可明确诊断,达到局部疾病控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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