AI Article Synopsis

  • - Cotyledonoid leiomyoma is a rare type of uterine fibroid that can appear malignant on ultrasound, often leading to drastic surgical decisions for treatment.
  • - The study reviewed 94 cases, noting that typical ultrasound features include a large, solid mass with high blood flow, and MRI showed unique characteristics like nodules and enhanced contrast.
  • - Most surgical approaches were hysterectomies, with low recurrence rates if fully excised; the unusual appearance during surgery and microscopic analysis suggest it is benign, influencing potential conservative treatment options.

Article Abstract

Cotyledonoidleiomyoma is an unusual uterine myoma due to some ultrasound features that mimic a malignant lesion facilitating the choice of radical surgery. This study aims to summarize the ultrasound and the magnetic resonance imaging aspects of this atypical lesion, and also discuss surgical treatment and pathological exam. It included all English case reports or case series until August 2021 found through PubMed, Google Scholar, and Scopus. A total of 94 cotyledonoid leiomyomas were reported, with a median tumor size of 12 cm. The typical ultrasound image is characterized by a large solid heterogeneous mass, with high vascularity, no shadowing, and indistinct margins within the myometrium. Magnetic resonance imaging shows the presence of merging isointense nodules to the myometrium in T1-weighted images, hyperintense in T2-weighted images, and contrast agent enhancement. Surgical treatment consists of hysterectomy (75 cases, 80%) or myomectomy (19 cases, 20%), without evidence of recurrence if complete. The placenta-like appearance observed during surgery supports this rare fibroid hypothesis. The intraoperative frozen section can be considered. Microscopically, no atypical cells, signs of mitotic activity or cell necrosis are found. To conclude, some preoperative and intraoperative aspects of this lesion are distinctive and may lead surgeons to opt for conservative surgery.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393327PMC
http://dx.doi.org/10.3390/ijerph18168521DOI Listing

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