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http://hdl.handle.net/20.500.12188/25014
Title: | Benign and malignant pigmented lesions of the female genital tract (FGT). Report of 15 cases. | Authors: | Kubelka, Katerina Basheska, Neli Yashar, Genghis Prodanova, Irina Ivkovski, Ljube Zografski, George |
Keywords: | female genital tract pigmented lesion nevus blue nevus malignant melanoma histopathology immunohistochemistry |
Issue Date: | Sep-2001 | Publisher: | Springer | Journal: | Virchows Archiv | Conference: | 18th European Congress of Pathology, September 8-13, 2001, Berlin, Germany. | Abstract: | Introduction: Benign and malignant pigmented lesions (PL) of the FGT are uncommon, predominantly affecting the vulva. Methods: We report the clinical and pathological features of the 15 PL of the FGT retrieved in a 12-year, retrospective analysis at our Department. Patient records and archival pathology specimens of 7 benign and 8 malignant PL of the FGT, were reviewed. Results: The mean age of all patients was 47 (range, 28-67). Three patients had vulvar nevi (2 intradermal and 1 dysplastic), while blue nevi ranging 2-10 mm in diameter were accidentally discovered in the endocervix of the hysterectomy specimens in four other patients. Vulvar primary malignant melanomas (PMMs) were uncommon (4 cases), comprising 2.5% of female PMMs and 4.3% of all vulvar malignancies diagnosed between 1989 and 2000. Contrary to other studies, all vulvar PMM in our series were of nodular type, ranging 3-13 mm in depth according to Breslow and III-IV level according to Clark. Within the same period, two patients with malignant PL of the uterine cervix were detected, accounting for 0.13% of all females with malignant cervical neoplasms. One of them had a PMM diagnosed in advanced clinical stage (FIGO III), and the other patient had an unusual pigmented squamous cell carcinoma in liB postoperative stage. There were also 2 cases of delayed unilateral ovarian metastases of cutaneous PMM. The diagnosis in all cases of non-vulvar pigmented lesions was confirmed by immunohistochemistry. Conclusions: Although uncommon, PL especially those affecting rare localizations must be considered as diagnostic possibility in FGT. | URI: | http://hdl.handle.net/20.500.12188/25014 | DOI: | 10.1007/BF02698641 |
Appears in Collections: | Faculty of Medicine: Conference papers |
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File | Description | Size | Format | |
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ECP 2001 pp335-6.pdf | 473.7 kB | Adobe PDF | View/Open | |
ECP 2001 cover.pdf | 75.39 kB | Adobe PDF | View/Open |
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