The medical literature suggests that about 3 out of 10 (30%) aggressive angiomyxoma
tumours will come back (recur].
mostly affects women and arises in the perineal and pelvic regions.
(AA) is a rare soft-tissue tumor that is typically found in the perineum of females of reproductive age.
The differential diagnosis might include a myxoid tumor such as myxoid neurofibroma or aggressive angiomyxoma
due to the presence of myxoid, proteinaceous, or mucinous contents.
Cellular angiofibroma can also be confused with aggressive vulvo-vaginal tumours like aggressive angiomyxoma
and solitary fibrous tumour (1, 5).
is a rare, myofibroblastic tumour, of pelvi-perineum of young women.
of the space of retzius: a case report.
There are 5 entities commonly accepted as myxomas: intramuscular myxoma, juxta articular myxoma, superficial angiomyxoma (or cutaneous myxoma), aggressive angiomyxoma
(usually pelvic and perineal regions) and myxoma of nerve sheath (myxoid neurothekeoma).
of pelvic parts exhibits estrogen and progesterone receptor positivity.
Fallopian tube prolapse mimicking aggressive angiomyxoma
Cutaneous angiomyxoma is to be differentially diagnosed and distinguished from other myxoidtumour including benign and low grade malignant myxoid lesions like aggressive angiomyxoma
, focal cutaneous mucinosis, myxoidneurothekeomas, myxoidneurofibroma, superficial acralfibromyxoma and myxoidliposarcoma.
1] CAF share pathological features of angiomyofibroblastoma and aggressive angiomyxoma
(AAM), but do not fall into either category.