Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature Review

Atypical polypoid adenomyoma (APAM) is a rare polypoid benign tumor of the uterus that causes irregular vaginal bleeding in women of reproductive age. It has the potential for malignant transformation, but it does not metastasize. APAM may coexist with endometrial hyperplasia and adenocarcinoma, usu...

Full description

Bibliographic Details
Main Authors: Tudor Butureanu, Ana-Maria Haliciu, Ana-Maria Apetrei, Ioana Pavaleanu, Razvan Vladimir Socolov, Raluca Anca Balan
Format: Article
Language:English
Published: MDPI AG 2023-12-01
Series:Life
Subjects:
Online Access:https://www.mdpi.com/2075-1729/13/12/2352
_version_ 1827574341657690112
author Tudor Butureanu
Ana-Maria Haliciu
Ana-Maria Apetrei
Ioana Pavaleanu
Razvan Vladimir Socolov
Raluca Anca Balan
author_facet Tudor Butureanu
Ana-Maria Haliciu
Ana-Maria Apetrei
Ioana Pavaleanu
Razvan Vladimir Socolov
Raluca Anca Balan
author_sort Tudor Butureanu
collection DOAJ
description Atypical polypoid adenomyoma (APAM) is a rare polypoid benign tumor of the uterus that causes irregular vaginal bleeding in women of reproductive age. It has the potential for malignant transformation, but it does not metastasize. APAM may coexist with endometrial hyperplasia and adenocarcinoma, usually leading to misdiagnosis. Histopathologically, it is a biphasic tumor, represented by the endometrioid glands with a complex histoarchitecture, with sometimes squamous morular metaplasia or cytologic atypia, interspersed with a fibromyomatous stroma. This tumor has a high incidence of recurrence. We present a very rare case of a 21-year-old patient, a virgin, without a significant medical history, with a bleeding mass occupying the vagina. The mass was excised using forceps, scissors, and a suture of the visible pedicle. After a four-year follow-up and no additional medical treatment, no relapse was observed. Given the risk of recurrence and progression, APAM might be treated via a hysterectomy in patients with no desire for pregnancy. Due to a lower recurrence rate, the conservative treatment of atypical polypoid adenomyoma performed via an operative hysteroscopy represents the best choice. Previously diagnosed in hysterectomy specimens, with the introduction of better-performing indirect imaging techniques, adenomyosis is a clinical entity that has the possibility of being diagnosed in the presurgical stage.
first_indexed 2024-03-08T20:35:49Z
format Article
id doaj.art-69736a5a39d449c7901a49b266ce8805
institution Directory Open Access Journal
issn 2075-1729
language English
last_indexed 2024-03-08T20:35:49Z
publishDate 2023-12-01
publisher MDPI AG
record_format Article
series Life
spelling doaj.art-69736a5a39d449c7901a49b266ce88052023-12-22T14:21:24ZengMDPI AGLife2075-17292023-12-011312235210.3390/life13122352Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature ReviewTudor Butureanu0Ana-Maria Haliciu1Ana-Maria Apetrei2Ioana Pavaleanu3Razvan Vladimir Socolov4Raluca Anca Balan5Department of Mother and Child, “Gr. T. Popa” University of Medicine and Pharmacy, 700115 Iasi, RomaniaDepartment of Mother and Child, “Gr. T. Popa” University of Medicine and Pharmacy, 700115 Iasi, RomaniaDepartment of Mother and Child, “Gr. T. Popa” University of Medicine and Pharmacy, 700115 Iasi, RomaniaDepartment of Mother and Child, “Gr. T. Popa” University of Medicine and Pharmacy, 700115 Iasi, RomaniaDepartment of Mother and Child, “Gr. T. Popa” University of Medicine and Pharmacy, 700115 Iasi, Romania“Elena Doamna” University Hospital of Obstetrics and Gynecology, 49, Elena Doamna St., 700398 Iasi, RomaniaAtypical polypoid adenomyoma (APAM) is a rare polypoid benign tumor of the uterus that causes irregular vaginal bleeding in women of reproductive age. It has the potential for malignant transformation, but it does not metastasize. APAM may coexist with endometrial hyperplasia and adenocarcinoma, usually leading to misdiagnosis. Histopathologically, it is a biphasic tumor, represented by the endometrioid glands with a complex histoarchitecture, with sometimes squamous morular metaplasia or cytologic atypia, interspersed with a fibromyomatous stroma. This tumor has a high incidence of recurrence. We present a very rare case of a 21-year-old patient, a virgin, without a significant medical history, with a bleeding mass occupying the vagina. The mass was excised using forceps, scissors, and a suture of the visible pedicle. After a four-year follow-up and no additional medical treatment, no relapse was observed. Given the risk of recurrence and progression, APAM might be treated via a hysterectomy in patients with no desire for pregnancy. Due to a lower recurrence rate, the conservative treatment of atypical polypoid adenomyoma performed via an operative hysteroscopy represents the best choice. Previously diagnosed in hysterectomy specimens, with the introduction of better-performing indirect imaging techniques, adenomyosis is a clinical entity that has the possibility of being diagnosed in the presurgical stage.https://www.mdpi.com/2075-1729/13/12/2352adenomyosispolypoidendometriosiscervicalmalignantpolyp
spellingShingle Tudor Butureanu
Ana-Maria Haliciu
Ana-Maria Apetrei
Ioana Pavaleanu
Razvan Vladimir Socolov
Raluca Anca Balan
Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature Review
Life
adenomyosis
polypoid
endometriosis
cervical
malignant
polyp
title Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature Review
title_full Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature Review
title_fullStr Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature Review
title_full_unstemmed Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature Review
title_short Prolapsed Atypical Polypoid Adenomyoma—A Case Report and Literature Review
title_sort prolapsed atypical polypoid adenomyoma a case report and literature review
topic adenomyosis
polypoid
endometriosis
cervical
malignant
polyp
url https://www.mdpi.com/2075-1729/13/12/2352
work_keys_str_mv AT tudorbutureanu prolapsedatypicalpolypoidadenomyomaacasereportandliteraturereview
AT anamariahaliciu prolapsedatypicalpolypoidadenomyomaacasereportandliteraturereview
AT anamariaapetrei prolapsedatypicalpolypoidadenomyomaacasereportandliteraturereview
AT ioanapavaleanu prolapsedatypicalpolypoidadenomyomaacasereportandliteraturereview
AT razvanvladimirsocolov prolapsedatypicalpolypoidadenomyomaacasereportandliteraturereview
AT ralucaancabalan prolapsedatypicalpolypoidadenomyomaacasereportandliteraturereview