Department of Pathology, College of Medicine, King Khalid University, Saudi Arabia.
Diagn Pathol. 2011 Apr 8;6:32. doi: 10.1186/1746-1596-6-32.
Blue nevi that arise from the Müllerian tract are rare melanocytic lesions. Several histopathologic variants of cellular blue nevi have been described. The angiomatoid variant is characterized by a vascular component, and is considered to be a rare variant. Few studies have explored the influence of pregnancy on melanocytic lesions.
A 29-year-old woman was presented with a pigmented vaginal lesion that increased gradually during pregnancy. A full term gynecologic examination showed a tumor mass protruding into the vaginal canal. The mass was resected during cesarean-section under the clinical impression of vaginal hemangioma.
Gross examination revealed a cystic mass measuring 6.0 × 4.3 × 3.5 cm, which was filled with dark friable material. Histologically, the mass showed a subepithelial cellular proliferation of heavily pigmented dendritic melanocytes with prominent vascular stroma. Cytologic pleomorphism, junctional activity, atypical mitosis, and necrosis were not found. The proliferation was immunoreactive for HMB-45, S-100 and melan-A, and non-immunoreactive for CD34, smooth muscle actin, and AE1/AE3. The MIB-1 proliferative index was less than 1%. The patient had a postoperative course without complication.
Angiomatoid giant cellular blue nevus arising from the vagina during pregnancy is extremely rare. The low proliferative index and absence of cytologic pleomorphism, or necrosis, supports a benign biological behavior. Clinical follow-up showed no evidence of recurrence at one year after the resection of the mass.
源于 Müller 氏管的蓝色痣是罕见的黑色素细胞病变。已经描述了几种细胞性蓝色痣的组织病理学变异型。血管型血管畸形的特征是血管成分,被认为是一种罕见的变异型。很少有研究探讨妊娠对黑色素细胞病变的影响。
一名 29 岁女性出现逐渐增大的色素性阴道病变,妊娠期间。足月妇科检查显示肿瘤肿块突出至阴道管。肿块在剖宫产期间切除,临床印象为阴道血管瘤。
大体检查显示一个囊性肿块,大小为 6.0×4.3×3.5cm,充满深褐色易碎物质。组织学上,肿块显示出上皮下细胞增殖,大量色素性树突状黑色素细胞和突出的血管基质。细胞学多形性、交界活动、非典型有丝分裂和坏死未发现。增殖对 HMB-45、S-100 和黑色素-A 呈免疫反应性,对 CD34、平滑肌肌动蛋白和 AE1/AE3 呈非免疫反应性。MIB-1 增殖指数小于 1%。患者术后无并发症。
妊娠期阴道起源的血管型巨大细胞蓝色痣极为罕见。低增殖指数和缺乏细胞学多形性或坏死支持良性生物学行为。临床随访显示,肿块切除一年后无复发证据。