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首页> 外文期刊>General thoracic and cardiovascular surgery >Desmoid-type fibromatosis arising in a bifid rib chest wall
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Desmoid-type fibromatosis arising in a bifid rib chest wall

机译:双层肋骨胸壁引起的Desmoid型纤维瘤病

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摘要

Desmoid-type fibromatosis is a rare soft tissue tumor and the chest wall is one of the common sites of its extra-abdominal occurrence. A bifid rib is one of the congenital rib abnormalities. We report a case of desmoid-type fibromatosis arising in a chest wall's bifid rib. A 42-year-old female complained of right chest pain without remarkable medical, traumatic, or familial history. Chest-computed tomography revealed a chest wall tumor located adjacent to a bifid costal cartilage of third rib. We performed chest wall resection of second and third ribs. Pathologically, the tumor was diagnosed a desmoid-type fibromatosis of the chest wall. We surmise mechanical stimulation due to the bifid rib may be related to the occurrence of the tumor. In case of desmoid-type fibromatosis without somatic gene mutation, traumatic history, wound, implants, or use of female hormonal agents, we should search also local congenital abnormality.
机译:DeaMoid型纤维瘤病是一种罕见的软组织肿瘤,胸壁是其腹部发生的常见遗址之一。 双歧肋是先天性肋骨异常之一。 我们举报了胸壁的双歧肋肋中出现的DeD系型纤维瘤病例。 一个42岁的女性抱怨右胸疼痛,没有出色的医学,创伤或家族历史。 胸部计算断层扫描显示胸壁肿瘤,位于第三肋的双歧肋骨软骨附近。 我们进行了第二和第三肋骨的胸壁切除。 病理上,肿瘤被诊断为胸壁的Demopoid型纤维瘤化。 我们推测由于BIFID肋引起的机械刺激可能与肿瘤发生有关。 如果没有体细胞基因突变,创伤史,伤口,植入物或使用女性激素剂的情况的情况下,我们应该搜索局部先天性异常。

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