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Prostatic-type tissue in the lower female genital tract: a morphologic spectrum, including vaginal tubulosquamous polyp, adenomyomatous hyperplasia of paraurethral Skene glands (female prostate), and ectopic lesion in the vulva
D.V. Kazakov, C.J. Stewart, D. Kacerovska, R. Leake, B. Kreuzberg, Z. Chudacek, M. Hora, M. Michal
The American journal of surgical pathology.
2010 ;
34 (7) :
950-955.
Language English Country United States
Document type Case Reports, Journal Article
Persistent link
https://www.medvik.cz/link/bmc12025682
- MeSH
- Choristoma MeSH
- Hyperplasia MeSH
- Middle Aged MeSH
- Humans MeSH
- Biomarkers, Tumor metabolism MeSH
- Neoplasms, Complex and Mixed metabolism pathology surgery MeSH
- Vaginal Neoplasms metabolism pathology surgery MeSH
- Vulvar Diseases pathology MeSH
- Polyps metabolism pathology surgery MeSH
- Prostate pathology MeSH
- Prostate-Specific Antigen metabolism MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Protein Tyrosine Phosphatases metabolism MeSH
- Urethra pathology MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
The investigators report a series of prostatic-type lesions occurring in the lower female genital tract. The cases included a 4.5-cm mass representing hyperplasia of the glandular and stromal tissue of paraurethral Skene gland, a small ectopic prostatic lesion in the vulva, and 4 tubulosquamous vaginal polyps. All lesions were immunopositive for prostate-specific antigen and/or prostatic acid phosphatase. A brief discussion of the earlier published material is included.
References provided by Crossref.org
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- $a The investigators report a series of prostatic-type lesions occurring in the lower female genital tract. The cases included a 4.5-cm mass representing hyperplasia of the glandular and stromal tissue of paraurethral Skene gland, a small ectopic prostatic lesion in the vulva, and 4 tubulosquamous vaginal polyps. All lesions were immunopositive for prostate-specific antigen and/or prostatic acid phosphatase. A brief discussion of the earlier published material is included.
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