Miyata Takashi, Fujiwara Yuta, Nishijima Koji, Futagami Fumio, Nakamura Takashi, Takamura Hiroyuki
Department of Surgery, Japanese Red Cross Kanazawa Hospital, Kanazawa, Ishikawa, 921-8162, Japan.
Department of General and Digestive Surgery, Kanazawa Medical University Hospital, 1-1 Daigaku, Uchinada, Kahoku, Ishikawa, 920-0293, Japan.
J Med Case Rep. 2019 Mar 18;13(1):66. doi: 10.1186/s13256-019-2008-9.
Malignant peritoneal mesothelioma is a rare aggressive tumor of the peritoneum. We report a rare case of resection of multiple localized malignant peritoneal mesotheliomas.
A 55-year-old Japanese woman was admitted to our hospital because liver tumors were detected by abdominal ultrasonography during a screening examination. Blood examination findings, including tumor makers, were within normal ranges. She had no evidence of exposure to asbestos. Computed tomography showed four hypervascular, round liver tumors, one in the lateral liver segment adjacent to the hepatic hilus, and the other three on the liver surface. Computed tomography angiography revealed that the tumor in the lateral segment had strong enhancement and was fed from the left gastric artery. In contrast, the other tumors showed no enhancement, and were fed from the right inferior phrenic artery. Abnormal accumulation was identified in the four tumors only with F-fluorodeoxyglucose positron emission tomography. It was very difficult to obtain a definitive preoperative diagnosis, but surgical resection was performed because we considered potential malignancy. Laparotomy revealed the principal site of the tumor in the lateral segment was on the hepatoduodenal ligament, and all other tumors were on the diaphragm. A left lobectomy and partial diaphragmatic resection were performed. The final pathological diagnosis was multiple malignant epithelioid mesotheliomas. Our patient has had no recurrence for 20 months postoperatively.
In general, malignant peritoneal mesotheliomas are classified as diffuse tumors, which are often unresectable and have a poor prognosis. However, early diagnosis and treatment, particularly with the localized type, as in our patient, could lead to long-term survival of the patient. We recommend that multiple malignant epithelioid mesotheliomas be included in the differential diagnosis for patients with subcapsular hepatic tumors.
恶性腹膜间皮瘤是一种罕见的侵袭性腹膜肿瘤。我们报告一例罕见的多发性局限性恶性腹膜间皮瘤切除术病例。
一名55岁的日本女性因在筛查检查中经腹部超声检测出肝脏肿瘤而入住我院。包括肿瘤标志物在内的血液检查结果均在正常范围内。她没有接触石棉的证据。计算机断层扫描显示肝脏有四个高血运的圆形肿瘤,一个位于肝门附近的肝外侧段,另外三个位于肝脏表面。计算机断层扫描血管造影显示外侧段的肿瘤有强烈强化,由胃左动脉供血。相比之下,其他肿瘤无强化,由右膈下动脉供血。仅通过F-氟脱氧葡萄糖正电子发射断层扫描在这四个肿瘤中发现异常聚集。术前很难做出明确诊断,但由于我们考虑到潜在的恶性可能,所以进行了手术切除。剖腹手术显示外侧段肿瘤的主要部位在肝十二指肠韧带,所有其他肿瘤位于膈肌上。进行了左叶切除术和部分膈肌切除术。最终病理诊断为多发性恶性上皮样间皮瘤。我们的患者术后20个月无复发。
一般来说,恶性腹膜间皮瘤被归类为弥漫性肿瘤,通常无法切除且预后较差。然而,早期诊断和治疗,特别是像我们患者这样的局限性类型,可能会使患者长期存活。我们建议将多发性恶性上皮样间皮瘤纳入肝包膜下肿瘤患者的鉴别诊断中。