Left inguinal dedifferentiated liposarcoma and primary unclassified sarcoma of the left lung as synchronous multiple sarcomas: a case report.

IF 0.7 Q4 SURGERY Surgical Case Reports Pub Date : 2024-10-28 DOI:10.1186/s40792-024-02043-0
Masao Kobayashi, Hidetoshi Satomi, Hisaya Chikaraishi, Hironobu Samejima, Julian Horiguchi, Ryu Kanzaki, Tomohiro Maniwa, Keiichiro Honma, Jiro Okami
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Abstract

Background: Pulmonary nodules in patients with soft tissue sarcomas are likely pulmonary metastases, whereas synchronous primary pulmonary sarcomas are rare. Without surgery, determining whether a solitary pulmonary nodule is a primary or metastatic nodule is difficult. Herein, we report a rare case of a primary pulmonary sarcoma that presented synchronously with a primary dedifferentiated liposarcoma.

Case presentation: A 77-year-old man presented to another hospital with left inguinal swelling and a suspected recurrent inguinal hernia. Computed tomography revealed a left inguinal mass and pure-solid nodule in the left lung and the patient was referred to our hospital for detailed examination and treatment. The inguinal mass was pathologically diagnosed as a dedifferentiated liposarcoma using needle biopsy, whereas bronchoscopic biopsy revealed histological findings suggestive of a sarcoma; however, the primary site could not be determined. Positron emission tomography-computed tomography revealed no high-accumulation lesions except for the two sarcomas. We decided to perform surgery on both sarcomas for diagnostic and curative purposes. The surgical specimens showed that the two sarcomas were different. Based on the immunohistochemical staining findings of MDM2, a left inguinal dedifferentiated liposarcoma and primary pulmonary unclassified sarcoma were diagnosed. The patient displayed no evidence of recurrence 1 year after surgery.

Conclusions: We encountered a rare case of synchronous multiple primary sarcomas, one presenting in the lung and the other in the soft tissue. Surgery was required to achieve a definitive diagnosis for the patient, who achieved disease-free survival at 1 year. This case suggests that proactive resection of pulmonary nodules in patients with soft tissue sarcomas may be feasible as a diagnostic treatment if complete resection is achieved.

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左腹股沟低分化脂肪肉瘤和左肺原发性未分类肉瘤为同步多发性肉瘤:病例报告。
背景:软组织肉瘤患者的肺结节很可能是肺转移瘤,而同步原发性肺肉瘤则很少见。在不进行手术的情况下,很难确定单发肺结节是原发性还是转移性结节。在此,我们报告了一例罕见的原发性肺肉瘤与原发性脂肪肉瘤同步出现的病例:一名 77 岁的男性因左腹股沟肿物和疑似复发性腹股沟疝到另一家医院就诊。计算机断层扫描显示左腹股沟肿块和左肺纯实性结节,患者被转到我院接受详细检查和治疗。腹股沟肿块经针刺活检病理诊断为脂肪肉瘤,而支气管镜活检显示组织学结果提示为肉瘤,但无法确定原发部位。正电子发射计算机断层扫描显示,除了这两个肉瘤外,没有其他高浓度病变。出于诊断和治愈的目的,我们决定对这两个肉瘤进行手术。手术标本显示,两个肉瘤并不相同。根据 MDM2 的免疫组化染色结果,诊断为左腹股沟低分化脂肪肉瘤和原发性肺部未分类肉瘤。患者术后一年无复发迹象:我们遇到了一例罕见的同步多发性原发性肉瘤病例,其中一个出现在肺部,另一个出现在软组织。患者需要通过手术获得明确诊断,并在术后 1 年实现了无病生存。该病例表明,如果能实现完全切除,对软组织肉瘤患者的肺部结节进行主动切除可能是可行的诊断性治疗方法。
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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