Liang Li, Zhang Yifen, Malpica Anais, Ramalingam Preetha, Euscher Elizabeth D, Fuller Gregory N, Liu Jinsong
Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Pathology, Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, People's Republic of China.
Mod Pathol. 2015 Dec;28(12):1613-20. doi: 10.1038/modpathol.2015.116. Epub 2015 Nov 13.
Gliomatosis peritonei, a rare condition often associated with immature ovarian teratoma, is characterized by the presence of mature glial tissue in the peritoneum. We retrospectively evaluated 21 patients with gliomatosis peritonei and studied their clinicopathologic features and immunophenotype. The patients' ages ranged from 5 to 42 years (median, 19 years). Their primary ovarian tumors consisted of immature teratoma (n=14), mixed germ cell tumors (n=6), and mature teratoma with a carcinoid tumor (n=1). Gliomatosis peritonei was diagnosed at the same time as primary ovarian neoplasm in 16 patients and secondary surgery in 5 patients. Also, 11 of 21 patients had metastatic immature teratoma (n=4), metastatic mature teratoma (n=2), or both (n=5). One patient developed glioma arising from gliomatosis peritonei. Seventeen patients had follow-up information and were alive with no evidence of disease (n=13), alive with disease (n=3), or alive with an unknown disease status (n=1). The follow-up durations ranged from 1 to 229 months (mean, 49 months; median, 23 months). Immunohistochemistry results demonstrated that SOX2 was expressed in all cases of gliomatosis peritonei and glioma with tissue available (nine of nine cases), whereas OCT4 and NANOG were negative in all cases with available tissue (eight of eight cases). In conclusion, both gliomatosis peritonei and glioma arising from it show a SOX2+/OCT4-/NANOG- immunophenotype. These findings demonstrated that gliomatosis peritonei is associated with favorable prognosis, although it is important to rule out potentially associated immature teratoma and malignant transformation. SOX2 may have an important role in the development of gliomatosis peritonei.
腹膜胶质瘤病是一种罕见疾病,常与未成熟卵巢畸胎瘤相关,其特征为腹膜内存在成熟神经胶质组织。我们回顾性评估了21例腹膜胶质瘤病患者,并研究了其临床病理特征和免疫表型。患者年龄为5至42岁(中位数19岁)。其原发性卵巢肿瘤包括未成熟畸胎瘤(n = 14)、混合性生殖细胞肿瘤(n = 6)和伴有类癌肿瘤的成熟畸胎瘤(n = 1)。16例患者在诊断原发性卵巢肿瘤的同时诊断出腹膜胶质瘤病,5例患者在二次手术时诊断出。此外,21例患者中有11例发生转移性未成熟畸胎瘤(n = 4)、转移性成熟畸胎瘤(n = 2)或两者皆有(n = 5)。1例患者发生源自腹膜胶质瘤病的胶质瘤。17例患者有随访信息,其中无疾病证据存活(n = 13)、带瘤存活(n = 3)或疾病状态不明存活(n = 1)。随访时间为1至229个月(平均49个月;中位数23个月)。免疫组化结果显示,在所有有组织样本的腹膜胶质瘤病和胶质瘤病例中(9例中的9例)SOX2均呈阳性表达,而在所有有组织样本的病例中(8例中的8例)OCT4和NANOG均呈阴性。总之,腹膜胶质瘤病及其所引发的胶质瘤均表现为SOX2+/OCT4-/NANOG-免疫表型。这些发现表明,腹膜胶质瘤病预后良好,尽管排除潜在相关的未成熟畸胎瘤和恶性转化很重要。SOX2可能在腹膜胶质瘤病的发生发展中起重要作用。