Source:http://linkedlifedata.com/resource/pubmed/id/16316848
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2005-11-30
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pubmed:abstractText |
The authors report a case of Leydig cell tumor in a 46-year-old woman who first presented with severe clinical hyperandrogenism and associated complex medical history. Investigations revealed markedly raised serum concentrations of testosterone (28.3 nmol/l) and free androgen index (54.4), whereas sex hormone binding globulin, random cortisol, androstenedione, 17-hydroxyprogesterone and dehydroepiandrosterone sulphate concentrations were all within the normal range. Transabdominal ultrasound and computed tomography scan of the pelvis and abdomen showed a slightly bulky right ovary, but no other abnormalities. An ovarian source of androgens was suspected and surgery was arranged. Following a three-year history of defaulting appointments due to agoraphobia, she underwent total abdominal hysterectomy with bilateral salpingo-oophorectomy and intraoperative selective ovarian venous sampling. Histopathological examination revealed a 2 cm Leydig cell tumor within the right ovary. Successful intraoperative ovarian venous sampling demonstrated significantly elevated testosterone levels (>260 nmol/l) from the right ovarian vein. Hyperandrogenaemia normalized post-operatively. The patient showed significant regression of clinical signs and symptoms, including the anxiety disorder. Clinical presentation, biochemistry and imaging modalities should allow to detect androgen-secreting ovarian tumors, while selective venous sampling should be reserved for patients whom uncertainty remains. The present case confirms that androgen-secreting ovarian tumors represent a diagnostic and therapeutic challenge. They have to be considered in the differential diagnosis of severe hyperandrogenism even in peri-menopausal women. Although selective venous sampling is of diagnostic value, however, its impact on future management should be considered on individual basis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0951-3590
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
238-41
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pubmed:meshHeading |
pubmed-meshheading:16316848-Androgens,
pubmed-meshheading:16316848-Fallopian Tubes,
pubmed-meshheading:16316848-Female,
pubmed-meshheading:16316848-Humans,
pubmed-meshheading:16316848-Hyperandrogenism,
pubmed-meshheading:16316848-Hysterectomy,
pubmed-meshheading:16316848-Leydig Cell Tumor,
pubmed-meshheading:16316848-Middle Aged,
pubmed-meshheading:16316848-Ovarian Neoplasms,
pubmed-meshheading:16316848-Ovariectomy,
pubmed-meshheading:16316848-Ovary,
pubmed-meshheading:16316848-Testosterone,
pubmed-meshheading:16316848-Tomography, X-Ray Computed,
pubmed-meshheading:16316848-Ultrasonography,
pubmed-meshheading:16316848-Veins,
pubmed-meshheading:16316848-Virilism
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pubmed:year |
2005
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pubmed:articleTitle |
Ovarian Leydig cell tumor in a peri-menopausal woman with severe hyperandrogenism and virilization.
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pubmed:affiliation |
Academic Unit of Obstetrics, Gynaecology and Reproductive Health, St Mary's Hospital, Manchester, UK. luciano.nardo@cmmc.nhs.uk
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pubmed:publicationType |
Journal Article,
Case Reports
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