Lugata John, Maringo Glory, Mremi Alex, Batchu Nasra, Mchome Bariki, Mbise Fredrick
Department of Obstetrics and Gynecology, Kilimanjaro Christian Medical Centre, Moshi, Tanzania; Faculty of Medicine, Kilimanjaro Christian Medical University College, Moshi, Tanzania.
Department of Obstetrics and Gynecology, Kilimanjaro Christian Medical Centre, Moshi, Tanzania; Faculty of Medicine, Kilimanjaro Christian Medical University College, Moshi, Tanzania.
Int J Surg Case Rep. 2024 Nov;124:110423. doi: 10.1016/j.ijscr.2024.110423. Epub 2024 Oct 10.
Mucinous cystadenoma is a benign cystic ovarian tumor arising from the surface epithelium of the ovary that usually presents with vague, unspecified abdominal symptoms. If not detected early, this tumor has the potential to grow to a substantial size and can present with huge abdominal distention leading to various compression symptoms. The reported incidence of giant ovarian cystadenoma in postmenopausal women is relatively unknown due to the widespread use of ultrasound and other radiological imaging modalities.
Here, we present a rare case of giant borderline mucinous cystadenoma in a 67-year-old female 10 years postmenopausal from Northern Tanzania with multiple comorbidities including hypertension and type 2 diabetes mellitus. She presented with abdominal distention which was of gradual onset for 1 year. Abdominal CT scan with contrast revealed a huge septated cystic mass occupying the entirety of the abdominal and pelvic cavities causing a mass effect on adjacent intra-abdominal structures. An intact 23-kg left ovarian cyst was removed, and a total abdominal hysterectomy (TAH) along with bilateral salpingo-oophorectomy (BSO) was performed. Post-operative recovery was excellent and the patient was discharged. The final histopathological report showed a borderline ovarian mucinous cystadenoma and the patient was managed conservatively after surgery.
In this case report, we discuss the condition's rarity especially in postmenopausal women, related reports in the literature, and the numerous difficulties clinicians face when encountering a patient with borderline mucinous cystadenoma. The rarity of borderline mucinous cystadenomas in postmenopausal women makes these cases clinically unusual, challenging diagnostic and therapeutic expectations.
This case report highlights the importance of thoroughly evaluating women with vague abdominal symptoms. While this condition is rare in postmenopausal women, its massive form can be dangerous if not diagnosed and managed promptly, with the potential to progress to malignancy. Greater awareness of this condition could lead to earlier detection and reporting of more cases.
黏液性囊腺瘤是一种起源于卵巢表面上皮的良性囊性卵巢肿瘤,通常表现为模糊、未明确的腹部症状。如果未早期发现,该肿瘤有可能生长到相当大的尺寸,并可出现巨大的腹部膨隆,导致各种压迫症状。由于超声和其他放射成像方式的广泛应用,绝经后女性中巨大卵巢囊腺瘤的报告发病率相对不明。
在此,我们报告一例罕见的巨大交界性黏液性囊腺瘤病例,患者为一名67岁的坦桑尼亚北部绝经后女性,患有多种合并症,包括高血压和2型糖尿病。她因腹部膨隆就诊,腹部膨隆逐渐出现,已持续1年。增强腹部CT扫描显示一个巨大的分隔囊性肿块,占据整个腹腔和盆腔,对相邻的腹腔内结构产生占位效应。切除了一个重达23千克的完整左侧卵巢囊肿,并进行了全腹子宫切除术(TAH)及双侧输卵管卵巢切除术(BSO)。术后恢复良好,患者出院。最终的组织病理学报告显示为交界性卵巢黏液性囊腺瘤,患者术后接受保守治疗。
在本病例报告中,我们讨论了该病症的罕见性,尤其是在绝经后女性中的情况、文献中的相关报道以及临床医生在遇到交界性黏液性囊腺瘤患者时所面临的诸多困难。绝经后女性中交界性黏液性囊腺瘤的罕见性使得这些病例在临床上不常见,对诊断和治疗预期构成挑战。
本病例报告强调了对有模糊腹部症状的女性进行全面评估的重要性。虽然这种病症在绝经后女性中罕见,但其巨大形式如果不及时诊断和处理可能很危险,有进展为恶性肿瘤的可能。提高对这种病症的认识可能会导致更早地发现和报告更多病例。