Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2022 Aug 18;68(2):123-127.
doi: 10.5387/fms.2022-08. Epub 2022 Jun 1.

A case of spontaneous parasitic myoma in a patient without a history of myomectomy treated laparoscopically

Affiliations
Case Reports

A case of spontaneous parasitic myoma in a patient without a history of myomectomy treated laparoscopically

Hyo Kyozuka et al. Fukushima J Med Sci. .

Abstract

Parasitic myoma (PM) is a rare disease in which multiple leiomyomas are intraperitoneally formed. Recently, an increasing number of cases due to specimen morcellation during minimally invasive surgery has been reported. We present the first case of a PM identified intraoperatively during laparoscopic hysterectomy. A 40-year-old Japanese multiparous woman presented to our hospital with heavy menstrual bleeding. She had no history of previous surgery. Magnetic resonance imaging showed uterine myomas. As the patient did not wish for further pregnancy, she underwent oral gonadotropin-releasing hormone antagonist therapy followed by a total laparoscopic hysterectomy. Intraoperatively, we identified a thumb-sized tumor on the left side of the peritoneum. Histopathological examination showed evidence of benign leiomyoma.

Keywords: gonadotropin-releasing hormone; hysterectomy; laparoscopic surgery; myoma; parasitic myoma.

PubMed Disclaimer

Conflict of interest statement

The authors have no potential conflicts of interest to declare.

Figures

Fig. 1.
Fig. 1.
Sagittal T2-weighted MRI Magnetic resonance imaging (MRI) showing enlarged uterine myomas that occupy the pelvic cavity (arrow).
Fig. 2.
Fig. 2.
Intraoperative laparoscopic image After laparoscopic hysterectomy is completed, we identified a thumb-sized tumor on the left side of the peritoneum (arrow). The patient had no previous surgical history.
Fig. 3.
Fig. 3.
Pathological findings for the resected tumor of the left side peritoneum. Hematoxylin and eosin, ×200 objective. Typical microscopic view of a benign leiomyoma, with no necrosis and without marked atypia (3a). The immunohistochemical evaluation of the resected tumor is positive for smooth muscle actin (3b), estrogen receptor (3c), and progesterone receptor (3d).
Fig. 4.
Fig. 4.
Coronal T2-weighted MRI After laparoscopic surgery, we reviewed the MRI scans taken before surgery. T2 weight MRI lesion indicates the presence of a 1.8 × 1.0 cm low-density solid tumor in the left peritoneum, apart from the uterine and uterine myoma (arrow).

References

    1. Murata T, Kyozuka H, Endo Y, et al. Preterm deliveries in women with uterine myomas: The Japan environment and children’s study. Int J Environ Res Public Health, 18: 2246, 2021. - PMC - PubMed
    1. D’Silva EC, Muda AM, Safiee AI, Ghazali WAHW. Five-Year Lapsed: Review of Laparoscopic Myomectomy versus Open Myomectomy in Putrajaya Hospital. Gynecol Minim Invasive Ther, 7: 161-166, 2018. - PMC - PubMed
    1. Kyozuka H, Fujimori K, Hosoya M, et al. The Japan environment and children’s study (JECS) in Fukushima prefecture: Pregnancy outcome after the Great East Japan earthquake. Tohoku J Exp Med, 246: 27-33, 2018. - PubMed
    1. Yoshino Y, Yoshiki N, Nakamura R, Iwahara Y, Ishikawa T, Miyasaka N. Large leiomyomatosis peritonealis disseminata after laparoscopic myomectomy: A case report with literature review. Int J Surg Case Rep, 77: 866-869, 2020. - PMC - PubMed
    1. Li PC, Lee MH, Wei YC, Hsu YH, Hong MK. Iatrogenic parasitic myoma with two recurrence times after subsequent myomectomy: A rare and complicated case report. Gynecol Minim Invasive Ther, 9: 154-158, 2020. - PMC - PubMed

Publication types