Document Detail


Applications of monoclonal anti-human inhibin alpha subunit in endometrial curettings.
MedLine Citation:
PMID:  14506965     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
AIMS: Using archival material, we studied the immunoreactivity and utility of monoclonal anti-human inhibin alpha subunit in the identification of chorionic villi (CV) and trophoblastic subpopulations in endometrial curettings (EC) from patients who had intra-uterine, ectopic, molar and, particularly, probable intra-uterine pregnancies. We also compared its expression with those of betaHCG, HPL and CAM 5.2. METHODS: The four groups of EC investigated included: Group 1, 15 patients with intra-uterine pregnancies (IUP); Group 2, 15 patients with tubal pregnancies (TP); Group 3, 15 patients with hydatidiform moles (HM); and Group 4, 20 patients with purported history of intra-uterine pregnancies (PIUP). Positive and negative control cases were from Groups 1 and 3 and Group 2, respectively. The test cases were from Group 4. Immunohistochemistry was performed on each case testing for expression of inhibin alpha, betaHCG, HPL and CAM 5.2. RESULTS: Trophoblastic populations, which included syncytiotrophoblast (ST), cytotrophoblast (CT) and intermediate trophoblast (IT), were absent in all 15 negative control cases (Group 2). The 30 positive control cases (Groups 1 and 3) revealed the following: (a) ST, CT and IT were identified in all cases and were positive for CAM 5.2, (b) inhibin alpha, betaHCG and HPL (except one case) were reactive for all cases with ST, but not CT, and (c) IT positivity for betaHCG, HPL and inhibin alpha was 67, 80-93 and 100%, respectively. From the 20 test cases (Group 4), the findings were: (a) CT was absent in all cases, (b) scattered ST cells, which were identified only in 10 cases, were positive for all antibodies, (c) scattered IT cells were present in 17 cases and showed 100% CAM 5.2 positivity, and (d) IT positivity for betaHCG, inhibin alpha and HPL was 58.8% (10/17), 76.5% (13/17) and 82.4% (14/17), respectively. Background staining was observed in 22 of 65 cases (33.8%) stained with betaHCG and HPL; half of these cases came from Group 3. Inhibin alpha and CAM 5.2 staining did not show this problem. CONCLUSIONS: We suggest that inhibin alpha is a useful antibody in diagnosing IUP and HM and in documenting intra-uterine gestations in cases with PIUP because it is a sensitive marker in immunolabelling IT and ST. Combined application of inhibin alpha and CAM 5.2 might be more useful than betaHCG and HPL because the latter showed background staining in one third of the cases.
Authors:
Leonardo D Santos; James L C Yong; Xiao Juan Wu
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Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  Pathology     Volume:  35     ISSN:  0031-3025     ISO Abbreviation:  Pathology     Publication Date:  2003 Jun 
Date Detail:
Created Date:  2003-09-24     Completed Date:  2004-02-10     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0175411     Medline TA:  Pathology     Country:  England    
Other Details:
Languages:  eng     Pagination:  217-23     Citation Subset:  IM    
Affiliation:
Department of Anatomical Pathology, South Western Area Pathology Service, Liverpool, NSW, Australia. leonardo.santos@swsahs.nsw.gov.au
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Biological Markers / analysis
Chorionic Gonadotropin, beta Subunit, Human / metabolism
Chorionic Villi / metabolism,  pathology
Dilatation and Curettage*
Endometrium / metabolism*,  pathology
Female
Humans
Hydatidiform Mole / metabolism,  pathology
Immunohistochemistry
Inhibins / metabolism*
Keratins / metabolism
Placental Lactogen / metabolism
Pregnancy
Pregnancy, Tubal / metabolism,  pathology
Retrospective Studies
Trophoblasts / metabolism,  pathology
Uterine Neoplasms / metabolism,  pathology
Chemical
Reg. No./Substance:
0/Biological Markers; 0/CAM 5.2 antigen; 0/Chorionic Gonadotropin, beta Subunit, Human; 0/inhibin-alpha subunit; 57285-09-3/Inhibins; 68238-35-7/Keratins; 9035-54-5/Placental Lactogen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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