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Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy
BACKGROUND: 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...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080280/ https://www.ncbi.nlm.nih.gov/pubmed/21477275 http://dx.doi.org/10.1186/1746-1596-6-32 |
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author | Al-Shraim, Mubarak M |
author_facet | Al-Shraim, Mubarak M |
author_sort | Al-Shraim, Mubarak M |
collection | PubMed |
description | BACKGROUND: 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. CASE: 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. RESULT: 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. CONCLUSIONS: 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. |
format | Text |
id | pubmed-3080280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30802802011-04-21 Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy Al-Shraim, Mubarak M Diagn Pathol Case Report BACKGROUND: 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. CASE: 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. RESULT: 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. CONCLUSIONS: 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. BioMed Central 2011-04-08 /pmc/articles/PMC3080280/ /pubmed/21477275 http://dx.doi.org/10.1186/1746-1596-6-32 Text en Copyright ©2011 Al-Shraim; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Al-Shraim, Mubarak M Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy |
title | Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy |
title_full | Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy |
title_fullStr | Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy |
title_full_unstemmed | Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy |
title_short | Angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy |
title_sort | angiomatoid giant cellular blue nevus of vaginal wall associated with pregnancy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080280/ https://www.ncbi.nlm.nih.gov/pubmed/21477275 http://dx.doi.org/10.1186/1746-1596-6-32 |
work_keys_str_mv | AT alshraimmubarakm angiomatoidgiantcellularbluenevusofvaginalwallassociatedwithpregnancy |