AI Article Synopsis

  • Cotyledonoid-dissecting leiomyoma is a rare type of uterine tumor that can be mistaken for cancer.
  • A case involved a 45-year-old woman who had a large pelvic mass, which was successfully diagnosed as this specific type of leiomyoma through laparoscopic biopsy.
  • The use of leuprorelin, a medication that reduces tumor size, prior to surgery demonstrated a significant decrease in the tumor, highlighting the benefits of minimally invasive diagnostic methods and preoperative treatment.

Article Abstract

Cotyledonoid-dissecting leiomyoma, a very unusual form of uterine leiomyoma, often leads to misdiagnosis as a malignant tumor. Here, we describe a case of a 45-year-old nulliparous woman who underwent a laparoscopic biopsy of a large pelvic mass consisting of multiple flaps. Histologically, the mass was composed of smooth muscle fascicle nodules separated by hydropic connective tissue, and exhibited extensive stromal hyalinization. The tumor was diagnosed as a cotyledonoid-dissecting leiomyoma based on the laparoscopic, pathological, and image findings. Prior to performing radical laparotomy, two courses of leuprorelin were administered in anticipation of tumor reduction and hypoperfusion, and the tumor size reduced remarkably. We demonstrated the utility of laparoscopic biopsy, considering its minimal invasiveness and diagnostic accuracy. Furthermore, the preoperative use of Gonadotropin-releasing hormone (GnRH) analogs to reduce surgical stress may be useful for treating cotyledonoid-dissecting leiomyomas.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11380131PMC
http://dx.doi.org/10.1177/2632010X241281240DOI Listing

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Article Synopsis
  • Leiomyomas are non-cancerous tumors of the uterine smooth muscle that can have various forms and are known to undergo secondary changes, sometimes resembling more serious conditions.
  • A rare type called cotyledonoid dissecting leiomyoma (CDL) can appear as large, abnormal masses, leading to misdiagnosis as cancer due to its size and complexity.
  • The article includes a case study of a 65-year-old woman with CDL, highlighting the need for awareness among healthcare professionals to prevent unnecessary aggressive treatments.
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Cotyledonoid dissecting leiomyoma (CDL) is a rare benign uterine leiomyoma that macroscopically shows multinodular placenta-like growth. Its border with the myometrial layer is unclear, making it clinically difficult to differentiate from uterine sarcoma. CDL is often misdiagnosed.

View Article and Find Full Text PDF
Article Synopsis
  • Cotyledonoid-dissecting leiomyoma is a rare type of uterine tumor that can be mistaken for cancer.
  • A case involved a 45-year-old woman who had a large pelvic mass, which was successfully diagnosed as this specific type of leiomyoma through laparoscopic biopsy.
  • The use of leuprorelin, a medication that reduces tumor size, prior to surgery demonstrated a significant decrease in the tumor, highlighting the benefits of minimally invasive diagnostic methods and preoperative treatment.
View Article and Find Full Text PDF

Cotyledonoid Dissecting Leiomyoma of the Uterus: A Benign Uterine Tumor That Resembles Malignancy.

J Minim Invasive Gynecol

October 2024

Gynecology and Obstetrics Department (Drs. Dong, Zheng and Guo), West China Second Hospital, Chengdu, Sichuan, China; Key Laboratory of Birth Defects and Related Diseases of Women and Children (Drs. Dong, Zheng, and Guo), Sichuan University, Ministry of Education, Chengdu, Sichuan, China. Electronic address:

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