Mesodermal mesenchymal polyp; wide introitus in young female.

Fibroepithelial stromal polyps Mesodermal mesenchymal polyp Wide introitus

Journal

International journal of surgery case reports
ISSN: 2210-2612
Titre abrégé: Int J Surg Case Rep
Pays: Netherlands
ID NLM: 101529872

Informations de publication

Date de publication:
31 Jul 2024
Historique:
received: 30 03 2024
revised: 18 07 2024
accepted: 24 07 2024
medline: 4 8 2024
pubmed: 4 8 2024
entrez: 3 8 2024
Statut: aheadofprint

Résumé

Mesodermal mesenchymal polyps (Fibroepithelial stromal polyps) are mesenchymal embryological structures that remain and grow to be an apparent polyp-like lesion in females of reproductive age. We present this case of mesodermal mesenchymal polyp in a young female arising at the hymenal ring of the vagina making the introitus very wide. We highlighted in our case the importance of recognizing mesenchymal lesions and their differential diagnosis to provide the patients with optimal care. A 24-years-old single female presented with a painless vaginal mass since birth, that increased in size after puberty. Upon examination, she was found to have an irregular smooth mass with around 4 × 4 cm of it protruding outside the vagina and easily reducible disfiguring and making the introitus wide. After performing Magnetic resonance imaging (MRI), findings were Suggestive of a Vulvovaginal mesenchymal tumor likely aggressive angiomyxoma. The patient underwent surgical vaginal mass excision, with hymenal repair, posterior and anterior vaginal wall reconstruction. The final diagnosis confirmed by tissue pathology was mesodermal mesenchymal polyp. Fibroepithelial polyps of the vagina (FEPV) is a rare benign neoplasm and most commonly asymptomatic apart from painless mass protruding or disfiguring the sensitive area. The variety of mesenchymal lesions that occur at the vulvovaginal region can be very challenging histopathologically and surgically due to their rarity and lack literature. Fibroepithelial polyps of the vagina (FEPV) remain an infrequent entity of pathologies affecting the female urogenital tract. We reported a rare case of concomitant FEPV and wide introitus affecting a young woman physically and psychologically. Therefore, preoperative clinical assessment and surgical approach along with psychological support is critical to provide the patient with the best outcome.

Identifiants

pubmed: 39096649
pii: S2210-2612(24)00865-4
doi: 10.1016/j.ijscr.2024.110084
pii:
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Pagination

110084

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Conflict of interest statement None.

Auteurs

Khalid Akkour (K)

Department of Obstetrics and Gynecology, College of Medicine, King Saud University, Riyadh, Saudi Arabia. Electronic address: kakkour@ksu.edu.sa.

Dana Aldabeeb (D)

Department of Obstetrics and Gynecology, College of Medicine, King Saud University, Riyadh, Saudi Arabia. Electronic address: daldabeeb1@ksu.edu.sa.

Metab Alkubeyyer (M)

Department of Radiology, College of Medicine, King Saud University, Riyadh, Saudi Arabia. Electronic address: malkubeyyer@ksu.edu.sa.

Mohammed Alswayyed (M)

Department of Pathology, College of Medicine, King Saud University, Riyadh, Saudi Arabia. Electronic address: malswayyed@ksu.edu.sa.

Ghadeer Alshaikh (G)

Department of Obstetrics and Gynecology, College of Medicine, King Saud University, Riyadh, Saudi Arabia. Electronic address: galshaikh@ksu.edu.sa.

Classifications MeSH