Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the Literature

Introduction. Pyomyoma, or suppurative leiomyoma, is a rare complication of uterine fibroids. It occurs most commonly in the setting of pregnancy, the immediate postpartum period, or postmenopausal status. It may also arise after recent uterine instrumentation, after uterine artery embolization, or...

Full description

Saved in:
Bibliographic Details
Main Authors: S. Read, J. Mullins
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Case Reports in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2018/1026287
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832552302015152128
author S. Read
J. Mullins
author_facet S. Read
J. Mullins
author_sort S. Read
collection DOAJ
description Introduction. Pyomyoma, or suppurative leiomyoma, is a rare complication of uterine fibroids. It occurs most commonly in the setting of pregnancy, the immediate postpartum period, or postmenopausal status. It may also arise after recent uterine instrumentation, after uterine artery embolization, or in immunocompromised patients. The most likely cause of pyomyoma is vascular compromise followed by bacterial seeding from direct, hematogenous, or lymphatic spread. Diagnosis is difficult, as the condition is rare, presents with vague symptoms, and is difficult to identify on imaging. Definitive diagnosis is only possible with surgery. Pathology shows a degenerating fibroid with hemorrhage, necrosis, cystic degeneration, and/or inflammatory change. Cultures of the pus contained within often show polymicrobial infection. Case Presentation. Our patient is a 24-year-old nulligravid female who presented with a surgical abdomen, fever, hypotension, and leukocytosis. She had no significant prior medical or surgical history, no history of uterine instrumentation, and no history of pelvic infection; she was not currently sexually active at the time of presentation. She was taken to the operating room, where she underwent diagnostic laparoscopy. This showed a ruptured pyomyoma originating in the left broad ligament. She then underwent laparoscopic myomectomy. She was transferred to the ICU intubated; she slowly recovered on IV antibiotics and was discharged home on postoperative day 10. Discussion. Pyomyoma is a rare condition and is even rarer in premenopausal patients without recent history of pregnancy or uterine instrumentation. This demonstrates an unusual case of spontaneous pyomyoma in the absence of risk factors, other than a history of known fibroids. Pyomyoma should be considered as a diagnosis in patients with sepsis, history of fibroids, and no other identifiable source of infection.
format Article
id doaj-art-7fc73bf5474e4723972872a424caaab8
institution Kabale University
issn 2090-6684
2090-6692
language English
publishDate 2018-01-01
publisher Wiley
record_format Article
series Case Reports in Obstetrics and Gynecology
spelling doaj-art-7fc73bf5474e4723972872a424caaab82025-02-03T05:58:59ZengWileyCase Reports in Obstetrics and Gynecology2090-66842090-66922018-01-01201810.1155/2018/10262871026287Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the LiteratureS. Read0J. Mullins1UConn Health, Department of OB/GYN, Farmington, CT, USAHartford Hospital, Department of OB/GYN, Hartford, CT, USAIntroduction. Pyomyoma, or suppurative leiomyoma, is a rare complication of uterine fibroids. It occurs most commonly in the setting of pregnancy, the immediate postpartum period, or postmenopausal status. It may also arise after recent uterine instrumentation, after uterine artery embolization, or in immunocompromised patients. The most likely cause of pyomyoma is vascular compromise followed by bacterial seeding from direct, hematogenous, or lymphatic spread. Diagnosis is difficult, as the condition is rare, presents with vague symptoms, and is difficult to identify on imaging. Definitive diagnosis is only possible with surgery. Pathology shows a degenerating fibroid with hemorrhage, necrosis, cystic degeneration, and/or inflammatory change. Cultures of the pus contained within often show polymicrobial infection. Case Presentation. Our patient is a 24-year-old nulligravid female who presented with a surgical abdomen, fever, hypotension, and leukocytosis. She had no significant prior medical or surgical history, no history of uterine instrumentation, and no history of pelvic infection; she was not currently sexually active at the time of presentation. She was taken to the operating room, where she underwent diagnostic laparoscopy. This showed a ruptured pyomyoma originating in the left broad ligament. She then underwent laparoscopic myomectomy. She was transferred to the ICU intubated; she slowly recovered on IV antibiotics and was discharged home on postoperative day 10. Discussion. Pyomyoma is a rare condition and is even rarer in premenopausal patients without recent history of pregnancy or uterine instrumentation. This demonstrates an unusual case of spontaneous pyomyoma in the absence of risk factors, other than a history of known fibroids. Pyomyoma should be considered as a diagnosis in patients with sepsis, history of fibroids, and no other identifiable source of infection.http://dx.doi.org/10.1155/2018/1026287
spellingShingle S. Read
J. Mullins
Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the Literature
Case Reports in Obstetrics and Gynecology
title Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the Literature
title_full Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the Literature
title_fullStr Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the Literature
title_full_unstemmed Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the Literature
title_short Spontaneous Ruptured Pyomyoma in a Nulligravid Female: A Case Report and Review of the Literature
title_sort spontaneous ruptured pyomyoma in a nulligravid female a case report and review of the literature
url http://dx.doi.org/10.1155/2018/1026287
work_keys_str_mv AT sread spontaneousrupturedpyomyomainanulligravidfemaleacasereportandreviewoftheliterature
AT jmullins spontaneousrupturedpyomyomainanulligravidfemaleacasereportandreviewoftheliterature