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Atypical compound nevus arising in mature cystic ovarian teratoma.

机译:非典型复合痣出现在成熟的囊性卵巢畸胎瘤中。

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Background: Mature cystic ovarian teratoma (MCOT) is the most common primaryovarian tumor. Rarely, MCOT may undergo malignant transformation. Melanoma arising primarily in MCOTis a rare event. Melanocytic nevi have also rarely been reported in MCOT. Case Report: A 28 year-oldfemale presented with a palpable, 4.6 cm, right pelvic mass on physical examination. Histologically,the cystic neoplasm demonstrated epidermis with numerous pilosebaceous units and respiratory-type epithelium(endoderm) surrounded by adipose tissue and cartilage (mesoderm). A 2.0x1.0 cm pigmented area correspondedto a nevus with architectural and cytologic features of the so-called "dysplastic nevus," including variable-sizednests of nevomelanocytes irregularly distributed on distorted rete ridges, bridging of nests betweenrete ridges, fibroplasia around rete ridges, and junctional shouldering beyond the dermal nevus. Thenevomelanocytes demonstrated moderate cytologic atypia. Diagnostic criteria of melanoma were not identified.Conclusions: Herein, we report, to the best of our knowledge, the first case of an atypical ("dysplastic")nevus, arising in a MCOT. No features of melanoma were present and the patient is disease-free at one-yearfollow-up. Rarely, melanocytic nevi and melanomas arise from the ectodermal component of MCOTs. Moreover,melanomas may arise de novo or in association with a nevus. Distinction between a melanocytic nevus,as in our case, and a primary melanoma is critical for determining the patient's prognosis and need foradditional therapy. As primary ovarian melanomas, like their skin counterpart, may arise from a precursorlesion, removal of a melanocytic nevus, such as this atypical nevus, could theoretically prevent melanomatransformation.
机译:背景:成熟的囊性卵巢畸胎瘤(MCOT)是最常见的原发性卵巢肿瘤。极少数情况下,MCOT可能会发生恶变​​。主要发生在MCOT中的黑色素瘤是罕见的事件。 MCOT中也很少报道黑素细胞痣。病例报告:一位28岁的女性经身体检查显示为可触及的4.6厘米右骨盆肿块。在组织学上,囊性肿瘤表现为表皮,表皮有许多皮脂腺单位和被脂肪组织和软骨(中胚层)包围的呼吸型上皮(内胚层)。一个2.0x1.0厘米的色素区域对应于具有所谓的“发育不良痣”的结构和细胞学特征的痣,包括不规则分布在畸变的网状脊上的可变尺寸的痣细胞,网状网桥之间的巢桥,网状网状增生,和交界的肩部超出真皮痣。绒毛黑色素细胞显示出中等的细胞学异型性。未确定黑色素瘤的诊断标准。结论:据我们所知,本文报道的第一例非典型(“发育异常”)痣是由MCOT引起。无黑色素瘤特征,患者随访一年无病。黑色素细胞痣和黑色素瘤很少来自MCOT的外胚层成分。此外,黑色素瘤可能从头出现或与痣相关。在本例中,黑素细胞痣与原发性黑色素瘤之间的区别对于确定患者的预后以及是否需要其他治疗至关重要。由于原发性卵巢黑色素瘤(如其皮肤对应物)可能源于前体病变,因此去除黑素细胞痣(例如这种非典型痣)在理论上可以预防黑色素瘤转化。

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