PDF(Pubmed)
Abstract：
UNASSIGNED: Spiradenocylindroma is a benign tumor of skin adnexal origin with overlapping features of two distinct neoplasms: spiradenoma and cylindroma. This cutaneous tumor typically presents on the head and neck and extracutaneous presentations are uncommon. The presentation described below involves a spiradenocylindroma within a mature ovarian teratoma is very rare.
UNASSIGNED: The aim of this article is to portray the diagnostic process of this unusual spiradenocylindroma presentation.
UNASSIGNED: A 65 year-old female with a left adnexal mass underwent ultrasonography and magnetic resonance imaging (MRI) which showed a left ovarian multiseptated lesion, with mural calcifications and projections into the mass. Excisional surgery was performed and histopathological examination revealed a spiradenocylindroma.
UNASSIGNED: Spiradenocylindroma is rare, hard to identify, and often misdiagnosed. Our study described the process of diagnosis and depicts the rare presentation of this lesion arising within a mature teratoma.
UNASSIGNED: The aim of this article is to portray the diagnostic process of this unusual spiradenocylindroma presentation.
UNASSIGNED: A 65 year-old female with a left adnexal mass underwent ultrasonography and magnetic resonance imaging (MRI) which showed a left ovarian multiseptated lesion, with mural calcifications and projections into the mass. Excisional surgery was performed and histopathological examination revealed a spiradenocylindroma.
UNASSIGNED: Spiradenocylindroma is rare, hard to identify, and often misdiagnosed. Our study described the process of diagnosis and depicts the rare presentation of this lesion arising within a mature teratoma.
摘要：
■螺旋腺泡瘤是皮肤附件起源的良性肿瘤，具有两种不同肿瘤的重叠特征：螺旋腺瘤和圆柱瘤。这种皮肤肿瘤通常出现在头颈部，皮外表现并不常见。以下描述的表现涉及成熟卵巢畸胎瘤中的螺旋腺苷酸瘤非常罕见。
■本文的目的是描述这种不寻常的螺旋腺泡瘤表现的诊断过程。
一名65岁女性左附件包块，接受了超声和磁共振成像（MRI）检查，显示左卵巢多间隔病变，壁膜钙化和肿块突出。进行了切除手术，组织病理学检查发现螺旋腺泡瘤。
■螺旋腺瘤很少见，很难辨认,经常被误诊。我们的研究描述了诊断过程，并描述了在成熟的畸胎瘤中出现的这种病变的罕见表现。
■本文的目的是描述这种不寻常的螺旋腺泡瘤表现的诊断过程。
一名65岁女性左附件包块，接受了超声和磁共振成像（MRI）检查，显示左卵巢多间隔病变，壁膜钙化和肿块突出。进行了切除手术，组织病理学检查发现螺旋腺泡瘤。
■螺旋腺瘤很少见，很难辨认,经常被误诊。我们的研究描述了诊断过程，并描述了在成熟的畸胎瘤中出现的这种病变的罕见表现。
