Uchime Kasiemobi Eberechukwu, Akinjo Oludolapo Andrea, Awolola Nicholas Awodele, Ohazurike Ephraim, Banjo Adekunbiola Aina, Uchechi Igbokwe
Department of Anatomic and Molecular Pathology, Lagos University Teaching Hospital, Lagos 102215, Lagos State, Nigeria.
Department of Anatomic Pathology and Forensic Medicine, Afe Babalola University Ado-Ekiti (ABUAD) Multi-system Hospital, Ado-Ekiti 360102, Ekiti state, Nigeria.
Ecancermedicalscience. 2023 Jun 5;17:1557. doi: 10.3332/ecancer.2023.1557. eCollection 2023.
Ovarian mucinous cystic tumours with mural nodules are rare tumours of the ovary that are often missed out during diagnosis. They are classified under the ovarian mucinous surface epithelial-stromal tumours. These mural nodules can be sarcoma-like (benign), anaplastic carcinoma, sarcomas, or mixed malignant (carcinosarcoma). However, very few cases of anaplastic malignant mural nodules have been reported. Here, we present a case of a borderline ovarian mucinous cystadenoma with anaplastic mural nodule that has sarcomatoid differentiation, in a 39-year-old woman who presented with a 1-year history of progressive abdominal swelling and pain. There were intraoperative findings of huge right ovarian cystic tumour with omental and umbilical deposits. Differential diagnosis of possible germ cell tumours, vascular tumours, melanoma, sarcoma and sarcoma-like nodules were ruled out with routine histology (Haematoxylin & Eosin), histochemical (reticulin) and immunohistochemical stains (CK AE1/3+, CD30+, AFP-, HCG-, EMA-, S100 protein-, CD31-, and CD34-) and the final diagnosis of a mural nodule of anaplastic carcinoma with sarcomatoid differentiation in a borderline ovarian mucinous cystadenoma established. Unfortunately, due to the aggressive nature of the tumour and disease progression, the patient passed on a few months after the surgery. This rare tumour, especially the ones with anaplastic carcinoma or mixed tumours, usually has an aggressive clinical course with most patients presenting late when the disease is advanced with poor clinical outcomes as is seen with the index patient. A high index of suspicion of this tumour with early detection and a multidisciplinary approach to its management is advised.
伴有壁结节的卵巢黏液性囊性肿瘤是卵巢的罕见肿瘤,诊断时常常被漏诊。它们归类于卵巢黏液性表面上皮-间质肿瘤。这些壁结节可以是肉瘤样(良性)、间变性癌、肉瘤或混合性恶性(癌肉瘤)。然而,间变性恶性壁结节的病例报道非常少。在此,我们报告一例39岁女性,患有伴有间变性壁结节且具有肉瘤样分化的交界性卵巢黏液性囊腺瘤,该患者有1年进行性腹部肿胀和疼痛病史。术中发现巨大的右卵巢囊性肿瘤伴有大网膜和脐部转移灶。通过常规组织学(苏木精和伊红染色)、组织化学(网状纤维染色)和免疫组织化学染色(细胞角蛋白AE1/3+、CD30+、甲胎蛋白-、人绒毛膜促性腺激素-、上皮膜抗原-、S100蛋白-、CD31-和CD34-)排除了可能的生殖细胞肿瘤、血管肿瘤、黑色素瘤、肉瘤及肉瘤样结节,最终确诊为交界性卵巢黏液性囊腺瘤伴间变性癌壁结节且具有肉瘤样分化。不幸的是,由于肿瘤的侵袭性和疾病进展,患者在手术后几个月去世。这种罕见肿瘤,尤其是那些伴有间变性癌或混合性肿瘤的,通常临床病程具有侵袭性,大多数患者就诊时疾病已进展到晚期,临床结局较差,本病例患者就是如此。建议对这种肿瘤高度怀疑,早期发现并采用多学科方法进行管理。