A rare case of pancreatic macrocystic serous cystadenoma in an adolescent: a case report and literature review

Author:

Chang Yu-Jui1,Lee Hung-Chang23ORCID,Yeung Chun-Yan234,Chen Wai-Tao23,Jiang Chuen-Bin23

Affiliation:

1. Department of Pediatrics, Taipei City Hospital Zhongxiao Branch, Taipei City

2. Division of Gastroenterology and Hepatology, Department of Pediatrics, MacKay Children’s Hospital, Taipei City

3. Department of Medicine, MacKay Medical College, New Taipei City

4. Department of Medical Research, MacKay Memorial Hospital, Taipei City

Abstract

While serous cystadenomas of the pancreas usually consist of small cysts, one rare variant has been reported to be composed of macrocysts. Herein, we present the case of the youngest patient with macrocystic serous cystadenoma (MSC) to be reported in the literature. The patient was a 17-year-old girl who presented with the major symptoms of a palpable abdominal mass accompanied by epigastric pain and vomiting for several months. A potential malignancy could not be excluded on the basis of imaging studies, which showed a large macrocystic pancreatic tumor that was 7 cm in diameter. Owing to the patient’s symptoms, after diagnosing the mass as a pancreatic cystic tumor with potential malignancy and large tumor size, surgical intervention was arranged. Pathological analysis of the biopsy sample suggested MSC. By reviewing the literature, we found several unique characters of MSCs that cause them to be frequently misdiagnosed as potential malignancies. Additionally, the age of MSC occurrence was found to be lower than of general serous cystadenomas. The potential of MSC should be kept in mind by clinicians when diagnosing young people with pancreatic macrocystic lesions.

Publisher

SAGE Publications

Subject

Biochemistry (medical),Cell Biology,Biochemistry,General Medicine

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