| CASE REPORT |
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| Year : 2020 | Volume
: 26
| Issue : 2 | Page : 166-169 |
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Desmoid-type fibromatosis of the splenic hilum: A rare tumor at an unusual location
Ana Sanchez-Gollarte1, Fernando Mendoza-Moreno1, Marina Perez-Gonzalez1, Manuel Diez-Alonso1, José María Muguerza-Huguet1, María Del Rocío Diez-Gago2, Fernando Noguerales-Fraguas1, Alberto José Gutierrez-Calvo1
1 Department of General and Digestive Surgery, Príncipe de Asturias Teaching Hospital, Alcalá de Henares, Madrid, Spain
2 Department of Emergency Medicine, Príncipe de Asturias Teaching Hospital, Alcalá de Henares, Madrid, Spain
Correspondence Address:
Dr. Ana Sanchez-Gollarte
9, Enrique Lopez Street, 28022, Madrid
Spain
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/njs.NJS_35_19
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Desmoid-type fibromatoses (DTFs), also known as desmoid tumors, are benign but infiltrative neoplasms that often appear next to previous surgical site. Intra-abdominal tumors usually involve the mesentery, but splenic hilum is an unusual localization. We present a case of a desmoid tumor of the splenic hilum laparoscopically resected in a 70-year-old male with a previous history of chromophobe renal cell carcinoma and ocular spindle melanoma. Although benign, desmoid tumors might be infiltrative and produce serious complications. Treatment remains controversial, ranging from surgery and medical therapies to observation. Management of DTF must be individualized, considering the risk of complications and recurrence.
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