Omental Serous Cystadenofibroma Mimicking Disseminated Malignancy: A Rare Pathology.

IF 0.5
Journal of medical cases Pub Date : 2026-04-29 eCollection Date: 2026-06-01 DOI:10.14740/jmc5316
Chibuike Ezeibe, Loren Walwyn-Tross, Dusan Perisic
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引用次数: 0

Abstract

Serous cystadenofibromas are rare benign epithelial ovarian tumors. They account for < 2% of benign ovarian tumors and typically affect individuals aged 15-65. In rare cases, these tumors present with scattered pelvic lesions resembling malignant dissemination. A 68-year-old female presented with pelvic pain. Pelvic sonogram revealed a 6 cm mass anterior to the cecum and bilateral cystic ovarian lesions measuring approximately 5 and 4 cm on the right and left, respectively. Subsequent pelvic magnetic resonance imaging (MRI) confirmed multicystic complex ovarian masses and a 6 cm multicystic mass along the cecum. Colonoscopy revealed no intrinsic rectal or sigmoid disease. She was subsequently referred to minimally invasive gynecology surgery and colorectal surgery for further management. Tumor markers and a ROMA panel were within normal limits. Computed tomography (CT) of abdomen/pelvis redemonstrated a multilobulated, cystic mass in the right lower quadrant with adjacent satellite lesions and bilateral cystic adnexal masses. Surgical intervention included robotic-assisted total laparoscopic hysterectomy, bilateral salpingo-oophorectomy, extensive lysis of adhesions, and infracolic omentectomy. Intraoperative findings revealed dense adhesions between the omentum, right adnexa, pelvic sidewall, and cecum. Frozen section revealed bilateral ovarian cystadenofibroma and omental tissue with benign cystic lesions resembling serous cystadenofibroma. Postoperatively, the patient had an uneventful recovery. Serous cystadenofibromas are associated with a favorable prognosis after complete resection of the tumor. The use of preoperative imaging and intraoperative frozen sections can help guide appropriate surgical management. However, these tumors pose diagnostic challenges due to their complex nature of adnexal masses with solid and cystic elements, often leading to misdiagnosis of malignancy. In rare cases, the presence of multiple lesions may be more consistent with multicentric development or independent primary lesions rather than true dissemination. Although malignancy must be carefully excluded, disseminated benign serous cystadenofibroma implants may radiologically and intraoperatively mimic peritoneal carcinomatosis, underscoring the importance of a broad differential diagnosis to guide intraoperative judgment and avoid overtreatment.

网膜浆液性囊腺纤维瘤模拟播散性恶性肿瘤:一种罕见的病理。
浆液性囊腺纤维瘤是一种罕见的卵巢良性上皮性肿瘤。它们占良性卵巢肿瘤的不到2%,通常影响15-65岁的个体。在罕见的病例中,这些肿瘤表现为分散的盆腔病变,类似恶性播散。68岁女性,骨盆疼痛。盆腔超声检查显示盲肠前部有一个6厘米的肿块,双侧卵巢囊性病变,左右分别约5厘米和4厘米。随后的盆腔磁共振成像(MRI)证实卵巢多囊复杂肿块和沿盲肠6厘米的多囊肿块。结肠镜检查未发现直肠或乙状结肠疾病。随后转至微创妇科手术和结直肠手术进行进一步治疗。肿瘤标志物和ROMA均在正常范围内。腹部/骨盆计算机断层扫描(CT)显示右下象限多分叶囊性肿块伴邻近的卫星性病变和双侧囊性附件肿块。手术干预包括机器人辅助全腹腔镜子宫切除术、双侧输卵管卵巢切除术、广泛粘连松解术和结肠下网膜切除术。术中发现大网膜、右附件、盆腔侧壁和盲肠之间有致密粘连。冷冻切片显示双侧卵巢囊腺纤维瘤和网膜组织,有类似浆液性囊腺纤维瘤的良性囊性病变。术后,患者恢复顺利。浆液性囊腺纤维瘤在完全切除肿瘤后预后良好。术前影像和术中冰冻切片的使用可以帮助指导适当的手术处理。然而,这些肿瘤由于其具有实体和囊性成分的附件肿块的复杂性而给诊断带来挑战,经常导致恶性误诊。在极少数情况下,多发病变的出现可能更符合多中心发展或独立的原发病变,而不是真正的播散。尽管恶性肿瘤必须仔细排除,但播散性浆液性囊腺纤维瘤植入物在放射学和术中可能与腹膜癌相似,这强调了广泛的鉴别诊断对指导术中判断和避免过度治疗的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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