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非寄生虫性囊肿起源的肝鳞状细胞癌:15年随访研究

Squamous cell carcinoma of the liver originating from non-parasitic cysts after a 15 year follow-up.

作者信息

Yagi Hiroshi, Ueda Masakazu, Kawachi Shigeyuki, Tanabe Minoru, Aiura Kouichi, Wakabayashi Go, Shimazu Motohide, Sakamoto Mituie, Kitajima Masaki

机构信息

Department of Surgery, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.

出版信息

Eur J Gastroenterol Hepatol. 2004 Oct;16(10):1051-6. doi: 10.1097/00042737-200410000-00016.

Abstract

Squamous cell carcinoma is an extremely rare primary liver tumour. A 42-year-old man presented at our hospital on 19 February 1986, with pain in the right upper quadrant of the abdomen and general fatigue, and reported an 8 year history of this complaint. Ultrasonography showed four cystic masses in the liver with a maximum diameter of 15 cm, one of which contained a solid component. A computed tomography (CT) scan confirmed a huge, predominantly cystic, mass in the liver with a small solid component and irregular wall. Calcifications were seen in the solid components. On 22 April 1986, a laparotomy was performed but the masses were too large to be removed. During 15 years of follow-up after the laparotomy, there had been no change seen in his abdominal CT scan. He subsequently arrived at our hospital again on 10 July 2001 with loss of appetite and of body weight. A CT scan showed a cyst in the liver of 25 cm in diameter with calcification that had a large solid part invading the liver. A post-mortem pathological dissection showed multiple cysts, the largest of which was 25 cm in diameter. They had large solid parts with calcification invading the liver. There were widespread metastatic lesions. Microscopic examination showed the tumour to be a well differentiated squamous cell carcinoma. To the best of our knowledge, this is the first report of a squamous cell carcinoma arising from 15 multiple non-parasitic hepatic cysts after a 15 year follow-up. Furthermore, 23 years had passed since the patient's symptoms appeared for the first time.

摘要

鳞状细胞癌是一种极为罕见的原发性肝癌。一名42岁男性于1986年2月19日前来我院就诊,主诉右上腹疼痛及全身乏力,称该症状已有8年病史。超声检查显示肝脏有4个囊性肿物,最大直径为15厘米,其中1个含有实性成分。计算机断层扫描(CT)证实肝脏有一个巨大的、以囊性为主的肿物,伴有小的实性成分和不规则的壁。实性成分可见钙化。1986年4月22日进行了剖腹手术,但肿物太大无法切除。剖腹手术后的15年随访期间,其腹部CT扫描未见变化。随后,他于2001年7月10日再次来到我院,出现食欲不振和体重减轻症状。CT扫描显示肝脏有一个直径25厘米的囊肿,伴有钙化,有一个大的实性部分侵犯肝脏。尸检病理解剖显示有多个囊肿,最大直径为25厘米。它们有大的实性部分伴有钙化并侵犯肝脏。有广泛的转移病灶。显微镜检查显示肿瘤为高分化鳞状细胞癌。据我们所知,这是首例经15年随访后由15个多发性非寄生虫性肝囊肿发生鳞状细胞癌的报告。此外,自患者首次出现症状以来已过去23年。

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