Gardner syndrome with giant abdominal desmoid tumor during pregnancy: a case report
| Autor: | Shan Huang, Yunbo Tan, Sita Pokhrel, Ziting Su, Liquan Jin, Yiming Chen, Hongbo Shi |
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| Rok vydání: | 2020 |
| Předmět: |
Adult
medicine.medical_specialty Adenoma lcsh:Surgery Case Report Fibromatosis Abdominal Familial adenomatous polyposis Pregnancy Gardner Syndrome medicine Humans Desmoid tumor Pathological Colectomy Fetus business.industry FAP lcsh:RD1-811 General Medicine medicine.disease Abdominal mass Surgery body regions Fibromatosis Aggressive Gestation Female medicine.symptom Tomography X-Ray Computed business Pregnancy Complications Neoplastic |
| Zdroj: | BMC Surgery BMC Surgery, Vol 20, Iss 1, Pp 1-5 (2020) |
| ISSN: | 1471-2482 |
| DOI: | 10.1186/s12893-020-00944-z |
| Popis: | Background Gardner syndrome is a subtype of familial adenomatous polyposis (FAP), characterized by a combination of adenomatous intestinal polyps and extracolonic lesions such as multiple osteomas, dental abnormalities, and soft tissue tumors. Although 12% of patients with intestinal polyposis of FAP may occur intra-abdominal desmoid tumors, pregnancy complicating with giant abdominal desmoid tumors is a relatively rare case. Case presentation A 28-year-old pregnant woman was diagnosed with Gardner syndrome in whom an intra-abdominal tumor was found a year after undergoing a laparoscopic total colectomy due to family adenomatous polyposis. At 32 weeks’ gestation, she presented to our department for the third time complaining upper abdominal pain caused by the giant abdominal mass about 21 × 12 cm2 in size. After multidisciplinary consultation and discussion, the decision of fetal preservation treatment was made. After the delivery of a baby girl, abdominal mass resection was performed, and pathological examination revealed a fibrous adenoma. The patient was discharged after a week and was uneventful in the follow-up for half a year. Conclusions Gardner syndrome is characterized by typical syndrome including family adenomatous polyposis and extra-intestinal tissue tumor. Were desmoid tumors rarely as large as fetus and local aggressively. In our case, we selected surgery to remove the intra-abdominal desmoid tumor after the natural delivery of the fetus and no abnormalities were observed during the 6 months follow-up. Women during pregnancy have an increased risk for the development of desmoid tumors, likely with the sex hormone to be one of the triggers. Therefore, we suggested that when a patient with Gardner syndrome desire to conceive again, they should go to the hospital for a regular review at least once every 3 months. |
| Databáze: | OpenAIRE |
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