Extraskeletal myxoid chondrosarcoma metastasis to a Meckel's diverticulum adenocarcinoma

Q4 Medicine
João Martins Gama , Rui Caetano Oliveira , Rúben Fonseca , Maria Augusta Cipriano , José Casanova
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引用次数: 0

Abstract

Extraskeletal myxoid chondrosarcoma is a rare soft tissue tumour with a high local and distant metastasis rate and limited response to chemotherapy.

Meckel's diverticulum is the most frequent congenital anomaly, and it is associated with a considerable risk of malignant transformation.

In this case report, we describe a 50-year-old female patient with a history of extraskeletal myxoid chondrosarcoma of the lower limb and metastasis to the forearm who went to the emergency department with abdominal pain. The investigations revealed a caecal volvulus. A lesion in the middle third of the ileum was incidentally discovered and removed during surgery.

Pathology examination revealed a Meckel's diverticulum adenocarcinoma, with metastasis of extraskeletal myxoid chondrosarcoma.

Resection was complete; however, the patient had diffuse metastatic pulmonary disease and died eight months later due to disease progression.

This mechanism of tumour-to-tumour metastasis is described in other locations, but, regarding the Meckel's diverticulum, this is a unique situation, previously unreported in the literature.

骨骼外肌样软骨肉瘤转移至梅克尔憩室腺癌
骨外肌软骨肉瘤是一种罕见的软组织肿瘤,具有较高的局部和远处转移率,对化疗的反应有限。梅克尔憩室是最常见的先天性畸形,与恶性转化的风险相当大。在本病例报告中,我们描述了一名因腹痛前往急诊就诊的 50 岁女性患者,她曾患下肢骨外肌软骨肉瘤并转移至前臂。检查结果显示有盲肠旋涡。病理检查显示为梅克尔憩室腺癌,并伴有骨外肌软骨肉瘤转移。病理检查显示,梅克尔憩室腺癌伴有骨骼外肌瘤样软骨肉瘤转移。切除手术很彻底,但患者出现了弥漫性肺转移性疾病,八个月后因病情恶化而死亡。
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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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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