Deodhar Kedar K, Suryawanshi Pallavi, Shah Milap, Rekhi Bharat, Chinoy R F
Department of Pathology, Tata Memorial Hospital, Parel, Mumbai, India.
Indian J Pathol Microbiol. 2011 Oct-Dec;54(4):730-5. doi: 10.4103/0377-4929.91508.
Immature teratoma (IT) of the ovary represents 1% of all ovarian cancers and 20% of malignant ovarian germ cell tumors. This retrospective study of 28 such cases aims to look at its morphological spectrum and to study the correlation of the grade and stage of the tumor with prognosis.
A retrospective study of 28 cases of IT of the ovary was done. Neuroepithelium was graded as grade I, II and III according to the standard criteria. The presence of immature mesenchyme was also looked for and similarly graded.
The median age for the cases was 19 years and abdominal pain was the commonest symptom. Neuroepithelium was seen in 26 cases (6 were grade I, 13 were grade II, and 7 were grade III); and two showed immature mesenchymal tissue (IM) only. IM was seen in all 28 cases, but no correlation with the grade of the IT of the ovary is found. The follow up is available in 23 cases ranging from 6 months to 78 months (median 33 months). Of these, 13 were stage I, 3 were stage II and 7 were stage III ITs. Out of 23 patients, 17 patients were alive without evidence of disease recurrence during the last follow up. Adverse events in the form of death and local recurrence occurred in 6 patients. One patient died of the disease at 7 months duration from the disease onset (stage III, grade II IT).
Morphological spectrum of IT of ovary is varied. Immature mesenchyme was seen in all the cases of IT of ovary and its presence should prompt a careful search for immature neuroepithelium. Stage I IT of ovary has better prognosis. Combination of surgery and chemotherapy can give longer survival even in recurrent disease.
卵巢未成熟畸胎瘤(IT)占所有卵巢癌的1%,占恶性卵巢生殖细胞肿瘤的20%。本对28例此类病例的回顾性研究旨在观察其形态学谱,并研究肿瘤分级和分期与预后的相关性。
对28例卵巢IT病例进行回顾性研究。根据标准标准,将神经上皮分为I级、II级和III级。还寻找未成熟间充质的存在并进行类似分级。
病例的中位年龄为19岁,腹痛是最常见的症状。26例可见神经上皮(6例为I级,13例为II级,7例为III级);2例仅显示未成熟间充质组织(IM)。所有28例均可见IM,但未发现其与卵巢IT分级相关。23例有随访资料,随访时间为6个月至78个月(中位33个月)。其中,13例为I期,3例为II期,7例为III期IT。23例患者中,17例患者在最后一次随访时存活且无疾病复发证据。6例患者出现死亡和局部复发等不良事件。1例患者在疾病发作7个月时死于该疾病(III期,II级IT)。
卵巢IT的形态学谱多样。所有卵巢IT病例均可见未成熟间充质,其存在应促使仔细寻找未成熟神经上皮。卵巢I期IT预后较好。手术和化疗联合即使在复发性疾病中也能延长生存期。