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Imaging features of a rare giant intra-abdominal aggressive angiomyxoma.
Tuan, Trinh Anh; Trang, Bui Huyen; Chau, Nguyen Thu Minh; Duy, Ngo Quang; Anh, Nguyen-Thi Hai; Hung, Nguyen Duy; Luc, Ceugnart; Duc, Nguyen Minh.
Afiliação
  • Tuan TA; Department of Radiology, Viet Duc Hospital, Hanoi, Vietnam.
  • Trang BH; Department of Radiology, Hanoi Medical University, Hanoi, Vietnam.
  • Chau NTM; Department of Radiology, Hanoi Medical University, Hanoi, Vietnam.
  • Duy NQ; Department of Radiology, Hanoi Medical University, Hanoi, Vietnam.
  • Anh NH; Department of Radiology, Hanoi Medical University, Hanoi, Vietnam.
  • Hung ND; Department of Radiology, Ha Giang General Hospital, Ha Giang, Vietnam.
  • Luc C; Department of Radiology, Alexandra Lepève Hospital, Dunkirk, France.
  • Duc NM; Department of Radiology, Viet Duc Hospital, Hanoi, Vietnam.
Radiol Case Rep ; 19(9): 4007-4011, 2024 Sep.
Article em En | MEDLINE | ID: mdl-39044857
ABSTRACT
Aggressive angiomyxoma (AAM) is a rare benign tumor that arises from connective tissue, prominently located in the vulva, vagina, perineum, and pelvis and is mainly found in women aged about 20-40 years old. Giant intraabdominal tumors have rarely been described. These tumors develop slowly over time and are often difficult to diagnose due to various clinical findings, especially in the early stages. Even though surgery is the primary treatment method, the possibility of complete resection is sometimes limited because the tumor tends to infiltrate nearby structures, leading to local recurrence. Only about 10% of AAM cases can be accurately diagnosed before treatment, which causes ineffective outcomes. This article demonstrates a case of giant intra-abdominal AAM precisely diagnosed by suspicious signs on CT and MRI scans before starting treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2024 Tipo de documento: Article