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胰腺浆液性囊腺瘤:33例患者的临床及病理特征

Serous cystadenoma of the pancreas: clinical and pathological features in 33 patients.

作者信息

Colonna Jorge, Plaza Jose Antonio, Frankel Wendy L, Yearsley Martha, Bloomston Mark, Marsh William L

机构信息

Department of Pathology, Ohio State University Medical Center, Columbus, Ohio 43210, USA.

出版信息

Pancreatology. 2008;8(2):135-41. doi: 10.1159/000123606. Epub 2008 Apr 1.

Abstract

AIM

To report the clinicopathological features of patients with serous cystadenomas of the pancreas.

METHODS

Thirty-three cases of serous cystadenoma diagnosed between 1977 and 2006 were retrieved from the files of the Ohio State University Medical Center. Clinical data and microscopic slides were reviewed.

RESULTS

The patients included 27 women and 6 men with an age range of 38-83 (mean 64.3) years. The clinical presentation included 13 patients with abdominal pain and 8 patients with abdominal mass; 9 tumors were found incidentally. Abdominal CT scans in 25 patients were interpreted as suspicious for carcinoma in 8 (32%), suspicious for serous cystadenoma in 8, neoplasm not otherwise specified in 8, and suspicious for a pseudocyst in 1. Only 7 patients underwent a preoperative biopsy, and 5 of these were diagnosed as having a serous cystadenoma. All but 2 of the patients underwent surgical resection of the tumor. The serous cystadenomas varied in size from 1.0 to up to 13 cm in maximum dimension, and all but one had a multicystic appearance. Of the 33 serous cystadenomas, 20 (61%) were located in the pancreatic tail, 4 (12%) in the pancreatic body, 4 in the pancreatic body and tail, and 5 (15%) in the head of the pancreas. Follow-up in 17 patients (median 3 years, range from 1 month to 11 years) showed no recurrence of serous cystadenomas. One patient had von Hippel-Lindau syndrome, 4 patients had diabetes mellitus, 3 patients had metastatic cancer, and 2 patients had ovarian tumors.

CONCLUSIONS

Serous cystadenoma is an uncommon neoplasm that can be confused with malignancy both clinically and radiologically; a correct diagnosis is important in order to provide an accurate prognosis.

摘要

目的

报告胰腺浆液性囊腺瘤患者的临床病理特征。

方法

从俄亥俄州立大学医学中心的档案中检索出1977年至2006年间诊断的33例浆液性囊腺瘤病例。回顾临床资料和显微镜切片。

结果

患者包括27名女性和6名男性,年龄范围为38 - 83岁(平均64.3岁)。临床表现包括13例腹痛患者和8例腹部肿块患者;9例肿瘤为偶然发现。25例患者的腹部CT扫描结果显示,8例(32%)被解读为可疑癌,8例可疑浆液性囊腺瘤,8例为未另行特指的肿瘤,1例可疑假性囊肿。仅7例患者接受了术前活检,其中5例被诊断为浆液性囊腺瘤。除2例患者外,所有患者均接受了肿瘤手术切除。浆液性囊腺瘤大小不一,最大直径为1.0至13厘米,除1例为单囊性外其余均为多囊性。33例浆液性囊腺瘤中,20例(61%)位于胰尾,4例(12%)位于胰体,4例位于胰体和胰尾,5例(15%)位于胰头。17例患者(中位随访3年,范围1个月至11年)的随访显示浆液性囊腺瘤无复发。1例患者患有冯·希佩尔-林道综合征,4例患者患有糖尿病,3例患者患有转移性癌,2例患者患有卵巢肿瘤。

结论

浆液性囊腺瘤是一种罕见肿瘤,在临床和放射学上都可能与恶性肿瘤混淆;正确诊断对于提供准确预后很重要。

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