Hayashi Kazuki, Kita Yusuke, Kawaguchi Yo, Hanaoka Jun
Department of General Thoracic Surgery, Omi Medical Center, Kusatsu, 525- 8585, Shiga, Japan.
Division of General Thoracic Surgery, Department of Surgery, Shiga University of Medical Science, Otsu, 520-2192, Shiga, Japan.
J Cardiothorac Surg. 2025 Oct 24;20(1):388. doi: 10.1186/s13019-025-03656-8.
Pseudomyxoma peritonei (PMP) is a rare neoplastic disease that can occasionally present with pulmonary metastases as an even rarer manifestation. Although cytoreductive surgery represents the primary treatment option for PMP, surgical management of pulmonary metastases presents unique challenges owing to their mucinous nature. The aim of this case series was to present key considerations for the surgical management of PMP lung metastases, particularly regarding solid-appearing nodules that are impalpable during surgical resection, requiring more extensive resection owing to the risk of recurrence.
Between November 2013 and May 2023, we performed a total of 13 surgical procedures for pulmonary metastases in seven patients with PMP at our institution. During these procedures, 18 pulmonary lesions were resected. Some patients underwent multiple surgeries; multiple lesions were resected in a single procedure in certain cases. Notable characteristics of PMP pulmonary metastases, attributed to their mucinous dissemination pattern, included cases wherein subpleural solid nodules that would typically be palpable in patients with conventional solid tumour metastases were non-palpable and cases requiring right upper lobectomy following repeated surgical margin recurrence. Median follow-up results showed a progression-free survival of 20.0 months and overall survival of 40.3 months. Three of the seven patients experienced postoperative recurrence, with two patients having intrapulmonary metastatic recurrence involving low-grade tumours.
Surgical resection can be an effective treatment option for PMP pulmonary metastases; however, careful patient selection and appropriate surgical planning are essential. The unique characteristics of PMP metastases necessitate specific surgical strategies. Since computed tomography-apparent solid nodules may be non-palpable intraoperatively and surgical margin recurrence should be avoided, selecting surgical approaches that minimise unnecessary lung palpation, such as preoperative marking or anatomical lung resection, is crucial. The mechanisms of PMP pulmonary metastasis development and progression remain unclear, warranting further research into blood-borne dissemination patterns and optimal surgical techniques for non-palpable lesions.
腹膜假黏液瘤(PMP)是一种罕见的肿瘤性疾病,偶尔可出现肺转移,这是一种更为罕见的表现。尽管减瘤手术是PMP的主要治疗选择,但由于肺转移灶的黏液性质,其手术管理面临独特挑战。本病例系列的目的是介绍PMP肺转移手术管理的关键考虑因素,特别是对于手术切除时无法触及的实性结节,由于复发风险需要更广泛的切除。
2013年11月至2023年5月期间,我们在本院为7例PMP患者进行了总共13次肺转移手术。在这些手术中,切除了18个肺部病变。一些患者接受了多次手术;在某些情况下,一次手术中切除了多个病变。PMP肺转移的显著特征归因于其黏液播散模式,包括以下情况:在传统实体瘤转移患者中通常可触及的胸膜下实性结节在PMP患者中无法触及,以及在手术切缘反复复发后需要进行右上叶切除的病例。中位随访结果显示无进展生存期为20.0个月,总生存期为40.3个月。7例患者中有3例术后复发,2例患者出现肺内转移复发,涉及低级别肿瘤。
手术切除可以是PMP肺转移的有效治疗选择;然而,仔细的患者选择和适当的手术规划至关重要。PMP转移的独特特征需要特定的手术策略。由于计算机断层扫描显示的实性结节在术中可能无法触及,应避免手术切缘复发,选择能尽量减少不必要肺触诊的手术方法,如术前标记或解剖性肺切除,至关重要。PMP肺转移发生和进展的机制仍不清楚,需要进一步研究血行播散模式和针对无法触及病变的最佳手术技术。