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[一例胸壁囊状水瘤]

[A case of cystic hygroma of the chest wall].

作者信息

Suzuki O, Ohata M, Ohmori K, Sezai Y, Okano T

机构信息

Second Department of Surgery, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Nihon Kyobu Geka Gakkai Zasshi. 1991 Jan;39(1):94-7.

PMID:2026923
Abstract

Hygroma is generally regarded as a benign tumor occurring favoritely in the cervical region of a child. Recently we have experienced a case of hygroma which was initially detected as a right chest wall tumor in a 16-year-old man, then was surgically diagnosed as cystic hygroma; chest roentgenography on a check up examination in his senior high school pointed out some anomaly, leading to his hospitalization. On admission, he had no subjective symptom, but chest roentgenography and CT confirmed an abnormal shadow in the right pulmonary area and a tumor with calcification on the right chest wall, respectively, so he was operated on for excisional biopsy. The tumor was extirpated together with the 7th intercostal muscle adhered to the tumor, and postoperative pathohistological examination led to diagnosis as cystic hygroma. Cystic hygroma of the chest wall is so rare that we would like to report this case, together with some addition consideration of related literature.

摘要

水囊瘤通常被认为是一种良性肿瘤,好发于儿童的颈部区域。最近我们遇到了一例水囊瘤病例,最初在一名16岁男性中被检测为右胸壁肿瘤,随后经手术诊断为囊性水囊瘤;他在高中体检时胸部X线检查发现了一些异常,导致他住院。入院时,他没有主观症状,但胸部X线检查和CT分别证实右肺区域有异常阴影以及右胸壁有一个钙化肿瘤,因此他接受了切除活检手术。肿瘤连同与肿瘤粘连的第7肋间肌一并切除,术后病理组织学检查诊断为囊性水囊瘤。胸壁囊性水囊瘤非常罕见,我们想报告此病例,并对相关文献进行一些补充探讨。

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