Results 41 to 50 of about 824 (126)

Aggressive angiomyxoma in pregnancy

open access: yesRare Tumors, 2014
Aggressive angiomyxoma (AA) is a rare, slow-growing mesenchymal neoplasm of vulvo-perineal region. Although AA is common in females of reproductive age, only a few cases during pregnancy have been documented in the English literature.
Prashant Goyal   +5 more
doaj   +1 more source

A Rare Clinical Presentation of Congenital Superficial Angiomyxoma: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
A pedunculated, cauliflower red‐colored, jelly mass in the left vulvar region (A) & (B). ABSTRACT Angiomyxoma is a rare atypical mesenchymal proliferation with two distinct forms, deep and superficial. Superficial Angiomyxoma tends to be benign with limited skin involvement.
Saman Al‐Zahawi   +6 more
wiley   +1 more source

Aggressive angiomyxoma presenting as a huge intra-abdominal mass in a pregnant Nigerian woman: a case report

open access: yesThe Pan African Medical Journal, 2015
Aggressive angiomyxoma is a rare, locally aggressive myxoid mesenchymal tumour that predominantly arises from the pelvis and perineum of young adult females. Occasional cases have been reported at unusual sites. Oestrogen and progesterone may play a role
Donatus Sabageh   +2 more
doaj   +1 more source

Aggressive (deep) angiomyxoma of the vulva: a case report 

open access: yesJournal of Medical Case Reports, 2022
Background Aggressive angiomyxoma of the vulva is a benign, slow-growing tumor originating from myxoid cells of connective tissue. The tumor is known for multiple local recurrences with a low tendency to metastasize.
Lajya Devi Goyal   +3 more
doaj   +1 more source

Comprehensive management of vulvovaginal cancers

open access: yesCA: A Cancer Journal for Clinicians, Volume 75, Issue 5, Page 410-435, September/October 2025.
Abstract Vulvar and vaginal cancers represent rare malignancies, with an incidence of 2.7 per 100,000 women for vulvar cancer, predominantly affecting women older than 60 years, although rising rates are observed in younger demographics. Approximately 90% of vulvar cancers are squamous cell carcinoma and frequently are associated with human ...
Angélica Nogueira‐Rodrigues   +5 more
wiley   +1 more source

Aggressive angiomyxoma of scrotum in a young male: A rare entity

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Aggressive angiomyxoma (AAM) is a rare mesenchymal benign myxoid tumor of the pelvis and perineum which occurs almost exclusively in adult females. It rarely occurs in males and involves scrotum.
Krishna Tadepalli, Vijaya Gattu
doaj   +1 more source

Scrotal Agressive Angiomyxoma

open access: yesÇukurova Üniversitesi Tıp Fakültesi Dergisi, 2014
Aggressive angiomyxoma is often a rare benign tumor, arising in the pelvic soft tissues and perineum. Aggressive angiomyxoma was described by Steper and Rosai first time in 1983. The main treatment method is wide-local excision.
Adem Altunkol   +5 more
doaj  

A Case of Primary Urethral Malignant Melanoma With Persistent Bleeding and Severe Anemia

open access: yesIJU Case Reports, Volume 8, Issue 4, Page 398-401, July 2025.
ABSTRACT Introduction Primary malignant melanomas of the urethra are extremely rare. The initial symptoms typically include hematuria or genital bleeding. This report describes a case of a massive primary urethral malignant melanoma with persistent bleeding.
Tatsuma Juichi   +6 more
wiley   +1 more source

Aggressive Angiomyxoma: A Rare Tumor of Male Pelvic Cavity

open access: yesActa Médica Portuguesa, 2018
Aggressive angiomyxoma is an uncommon, benign, slow-growing, and locally infiltrative soft tissue neoplasm which is located primarily in the genital region and pelviperineal interstitial tissue of female patient in the fourth decade of life.
Suleyman Utku Celik   +3 more
doaj   +1 more source

Orbital Angiomyxoma: Bridging Diagnostic Gaps and Enhancing Surgical Outcomes

open access: yesClinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Orbital angiomyxoma, though rare, presents with gradual proptosis and associated ocular symptoms. Early diagnosis through imaging and histopathology, followed by precise surgical intervention, can significantly improve outcomes, reducing proptosis and ensuring recovery with appropriate follow‐up care.
Rajat Agarwal   +6 more
wiley   +1 more source

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