Anwar Ayesha, Kasi Anup
Allama Iqbal Medical College
University of Kansas
The infiltration of malignant cells into the serous membrane that lines the abdominal cavity, viscera, and coelom in amniotes is termed peritoneal surface malignancy or peritoneal cancer. This condition is categorized into primary and secondary types. Primary mesothelioma arises from the de novo development of cancer in the mesothelium of the abdomen. In contrast, secondary peritoneal cancer occurs due to the spread of tumor cells from other locations into the peritoneal cavity. Primary peritoneal cancer is further classified based on histology, with terms such as extraovarian primary peritoneal carcinoma (EOPPC), serous surface papillary carcinoma, papillary serous carcinoma of the peritoneum, extraovarian Mullerian adenocarcinoma, and normal-sized ovarian carcinoma syndrome being used to describe this type. Additional types of peritoneal cancer include malignant peritoneal mesothelioma, multicystic mesothelioma, leiomyosarcomas, leiomyomatosis peritonealis disseminata, and desmoplastic small round cell tumor. Swerdlow initially reported EOPPC as "mesothelioma of pelvic peritoneum" in a case study published in 1959. EOPPC behaves similarly to serous ovarian cancer, often with minimal involvement of the ovaries. While these types exhibit varied histological features, they share similarities in presentation, diagnostic evaluation, and treatment approaches (see Light Microscopic Features of Types of Peritoneal Cancer). Secondary or metastatic peritoneal carcinomatosis commonly originates from primitive malignancies affecting gastrointestinal and gynecological structures. Metastasis may occur through transcoelomic, vascular, or lymphatic routes, with the first description dating back to 1931, illustrating the local spread of ovarian cancer. Primary peritoneal cancer is typically classified as stage III or IV, while metastasis is categorized as stage IV. The nonspecific clinical presentation often results in delayed diagnosis, decreasing survival rates. Surgical resection and intraperitoneal chemotherapy are considered critical approaches for disease elimination. Nevertheless, advancements in understanding peritoneal physiology and tumor seeding pathways, coupled with technological progress, have facilitated the development of more effective treatment modalities. In the absence of extensive systemic disease, achieving locoregional control of the cancer holds promise in managing this late-stage condition.
恶性细胞浸润羊膜动物腹腔、内脏和体腔的浆膜,称为腹膜表面恶性肿瘤或腹膜癌。这种情况分为原发性和继发性。原发性间皮瘤起源于腹部间皮的癌症新发。相比之下,继发性腹膜癌是由于肿瘤细胞从其他部位扩散到腹腔所致。原发性腹膜癌根据组织学进一步分类,使用诸如卵巢外原发性腹膜癌(EOPPC)、浆液性表面乳头状癌、腹膜乳头状浆液性癌、卵巢外苗勒腺癌和正常大小卵巢癌综合征等术语来描述这种类型。其他类型的腹膜癌包括恶性腹膜间皮瘤、多囊性间皮瘤、平滑肌肉瘤、播散性腹膜平滑肌瘤病和促纤维增生性小圆细胞瘤。斯韦德洛在1959年发表的一项病例研究中最初将EOPPC报告为“盆腔腹膜间皮瘤”。EOPPC的行为与浆液性卵巢癌相似,卵巢受累通常较轻。虽然这些类型表现出不同的组织学特征,但它们在临床表现、诊断评估和治疗方法上有相似之处(见腹膜癌类型的光镜特征)。继发性或转移性腹膜癌通常起源于影响胃肠道和妇科结构的原发性恶性肿瘤。转移可能通过体腔、血管或淋巴途径发生,首次描述可追溯到1931年,说明了卵巢癌的局部扩散。原发性腹膜癌通常分类为III期或IV期,而转移则分类为IV期。非特异性的临床表现常常导致诊断延迟,降低生存率。手术切除和腹腔内化疗被认为是消除疾病的关键方法。然而,对腹膜生理学和肿瘤种植途径的认识进步,加上技术进步,促进了更有效治疗方式的发展。在没有广泛全身疾病的情况下,实现癌症的局部区域控制有望管理这种晚期疾病。