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T Romer

Publications and source records attributed to T Romer.

13 recordsLinked to original sources

[In Process Citation]

OBJECTIVE: Endometriosis is one of the most common benign gynaecological diseases. Its aetiology is uncertain and there are many unanswered questions about its pathogenesis and treatment. MATERIAL AND METHODS: Medline search of relevant publications. RESULTS: Particularly the early stages of endometriosis, usually located in the peritoneum, are metabolically highly active and, even from the start, set in motion a vicious circle of progressive organ destruction, adhesions and inflammatory processes. This can lead to chronic cyclic or acyclic pains and/or sterility. Invasiveness and potential for progression are based on the secretion of prostaglandin derivatives and numerous cytokines which, together with the gradual failure of immune resistance and the local hormonal environment, usually dominated by oestrogen, are responsible for the progressive nature of around 50% of endometriosis cases. The estimated incidence of active, progressive endometriosis is 21,000 new cases per year in Germany, placing it on a par with prostate cancer. Subtle microscopic and morphological grading of the activity of the lesions is crucial to the choice of treatment. Early results of clinical trials indicate that the highest pregnancy rates and the lowest recurrence rates at follow-up can be achieved with individualised hormonal and surgical treatment of active endometriosis, even for mild or minimal endometriosis, in comparison with the laparoscopic removal of lesions alone. CONCLUSIONS: The combined use of hormonal and surgical treatment could become the new gold standard for treating active endometriosis.

Journal Article↗

[In Process Citation]

Endometriosis is a proliferative disease, which is often diagnosed with delay. Laparoscopy and histology are necessary for diagnosis. Different factors influence the success of therapy. Proliferative markers are very important for the differential diagnosis of active and inactive endometriosis. In a study it could be shown that endometriosis with high proliferative activity (high expression of Ki67) has a high response rate to GnRH-analogues treatment. Active endometriosis has to b distinguished to select an optimal treatment. A high proliferative activity of endometriosis should be treated with a hormonal-surgical combination.

Journal Article↗

Evaluation of 21-deoxycortisol as a marker for the detection of heterozygous carriers of 21-hydroxylase deficiency.

The study was aimed at evaluation of usefulness of determination of blood serum 21-deoxycortisol concentration for the detection of heterozygous carriers of incomplete block of 21-hydroxylase synthesis leading to adrenal hyperplasia. An earlier observation of the authors that the determination of 21-deoxycortisol is a more sensitive marker than 17-hydroxyprogesterone for diagnosing this genetic defect provided the motivation for undertaking this study. The levels of 21-deoxycortisol and 17-hydroxyprogesterone were determined in blood serum by using radioimmunoassay methods in 18 mothers and 21 fathers of children born with 21-hydroxylase deficiency, before and after intravenous administration of ACTH. As a control group served 15 women and 11 men of the corresponding age. Unlike 17-hydroxyprogesterone, 21-deoxycortisol levels were significantly higher both in women (20.5 +/- 12.6 ng/dl) and in men (21.2 +/- 14.4 ng/l) suspected of being heterozygous carriers, both before and after stimulation with ACTH, as compared to those in the control group (6.9 +/- 3.6 in women and 7.9 +/- 2.8 in men). Only in three women and in two men suspected of carrying the defective gene the values of 21-deoxycortisol were in normal range. The results obtained demonstrated evidently that 21-deoxycortisol can be regarded as a more sensitive marker for the detection of heterozygous carriers of 21-hydroxylase deficiency than 17-hydroxyprogesterone and the determination of 21-deoxycortisol is more useful for diagnosing this genetic defect.

17-alpha-Hydroxyprogesterone↗