Hariri Mohamad Moafak, Farho Mohamad Ali, Kourdy Alaa, AlHammoud Hiba Allah, Alawad Kawthar, Ghabreau Lina
Faculty of Medicine, University of Aleppo, Aleppo, Syrian Arab Republic.
Faculty of Pharmacy, University of Aleppo, Aleppo, Syrian Arab Republic.
Case Rep Womens Health. 2024 Apr 4;42:e00604. doi: 10.1016/j.crwh.2024.e00604. eCollection 2024 Jun.
Cotyledonoid dissecting leiomyoma (CDL) is a rare uterine tumor with unique clinical and histological features. We present a case of a 46-year-old woman with a 3-month history of left-flank pain radiating to the back. The patient had a history of infertility and a previous miscarriage. Ultrasound revealed a solid tissue mass suggestive of a degenerated fibroid. Laparoscopy identified subserosal leiomyoma and leiomyoma in the broad ligament. Histologically, CDL is characterized by disorganized smooth muscle with hyaline degeneration and no evidence of malignancy. Clinically, CDL can present with a variety of symptoms, including heavy menstrual bleeding, pelvic pain, and infertility. The coexistence of CDL and adenomyosis is exceedingly rare. This case highlights the importance of considering CDL in the differential diagnosis of pelvic mass, malignant neoplasms, and infertility, even with atypical symptoms. It also emphasizes the value of cooperation between clinicians and pathologists for accurate diagnosis and management of CDL. Adenomyosis in this case further complicated the diagnosis and highlighted the need for an index of suspicion for this rare condition.
子叶样切割性平滑肌瘤(CDL)是一种具有独特临床和组织学特征的罕见子宫肿瘤。我们报告一例46岁女性病例,该患者有3个月左侧胁腹疼痛并向后背部放射的病史。患者有不孕史且曾有过一次流产。超声检查发现一个实性组织肿块,提示为变性肌瘤。腹腔镜检查发现浆膜下平滑肌瘤和阔韧带内平滑肌瘤。组织学上,CDL的特征是平滑肌排列紊乱伴透明变性,无恶性证据。临床上,CDL可表现出多种症状,包括月经过多、盆腔疼痛和不孕。CDL与子宫腺肌病同时存在极为罕见。该病例强调了在盆腔肿块、恶性肿瘤和不孕的鉴别诊断中考虑CDL的重要性,即使症状不典型。它还强调了临床医生和病理医生合作对于准确诊断和管理CDL的价值。该病例中的子宫腺肌病使诊断进一步复杂化,并突出了对这种罕见疾病保持怀疑指数的必要性。