[A Case of Desmoid-Type Fibromatosis of the Mesentery of Small Intestine].
Gan To Kagaku Ryoho
; 51(3): 334-335, 2024 Mar.
Article
em Ja
| MEDLINE
| ID: mdl-38494823
ABSTRACT
Desmoid-type fibromatosis is a relatively rare disease, often associated with familial adenomatous polyposis and a history of abdominal surgery. A 43-year-old male patient presented with abdominal pain and contrast-enhanced CT showed a mass in the lower abdomen. The mass was a 4×4×3 cm white, dense tumor with a wreath-like arrangement of eosinophilic spindle-shaped cells. Immunostaining showed KIT(-), CD34(-), desmin(-), ß-catenin(+), SMA(few+), and the diagnosis was desmoid-type fibrosis. Six months after surgery, there was no apparent recurrence.
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Base de dados:
MEDLINE
Assunto principal:
Fibromatose Agressiva
/
Fibromatose Abdominal
/
Polipose Adenomatosa do Colo
Limite:
Adult
/
Humans
/
Male
Idioma:
Ja
Revista:
Gan To Kagaku Ryoho
Ano de publicação:
2024
Tipo de documento:
Article