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العنوان
Azoospermia\
الناشر
Mohamed Hisham Mohamed Farid ,
المؤلف
Azaam,Mohamed Hisham Mohamed Farid
هيئة الاعداد
باحث / محمد هشام محمد فريد عزام
مشرف / محمود محمد البيومى
مشرف / خالد محيي الدين منيب حسين
مشرف / لا يوجد
الموضوع
Dermatology.
تاريخ النشر
1988 .
عدد الصفحات
185p.:
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الأمراض الجلدية
تاريخ الإجازة
1/1/1988
مكان الإجازة
جامعة بنها - كلية طب بشري - جلديه
الفهرس
Only 14 pages are availabe for public view

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from 201

Abstract

Azoospermia is an important. cause of male infertility in which the ejaculated semen is devoid of any spermatozoa. Templeton (1983) found that azoospermia account for 9.2% of new couples attending the infertility clinic. In U.S.A. approximately 15 out of every 100 marriages are barren and do not produce progeny. Defects in the husbands reproductive system are responsible for somewhat over 50% of the cases (Wong . et al., 1973).
According to Wong et al., (1978), azoospermia is classified into testicular, pre-testicular and post-testicular. Testicular azoospermia is subdivided into absent testis, small sized testis and normal sized testis. Pretesticular azoospermia may be due to hypogonadotropism, oestrogen excess or androgen excess. Post-testicular or obstructive azoospermia may be at the level of pre-epididymal, epididymal, vasal or ejaculatory duct.
In order to evaluate a case of azoospermia, careful history must be taken and physical examination
have to be done. At least two or three specimens of semen should be examined before a diagnosis of
azoospermia is made (Salama, 1982c).
The level of gonadotrophins (F.S.H. and L.H.) in serum must be done. High F.S.H. levels when associated with small testes indicates severe testicular damage (Hargreave and Jequier, 1978).
Testicular biopsy is indicated for azoospermic patients in whom the testicles are essentially normal on physical examination and whose serum F.S.H. levels are normal or only mildly elevated, biopsy provides critical information. In this patient group, scrotal exploration and testicular biospy allow the clinician to distinguish between ductal obstruction and ablative testicular pathology (Coburn et al., 1987).
Other investigations as Karyotyping, X-ray skull, vasography and chemical analysis of semen are to be done in order to detect the aetiology.
Congenital and acquired hpygonadotropic
hypogonadism can be successfuly treated with gonadotropins (Vermeulen, 1982). The generally recommended treatment is a combination of H.C.G. (human chorionic gonadotropin) and H.M.G (human menopausal gonadtropin) when spermatogenesis is desired (Rostom, 1983c). Epididymal obstruction is conventionally treated by means of the operation vaso-epididymostomy. The basis for this operation is the formation of a fistutal between the efferent ductual or the epididymal duct and vas deferens. Vaso-vasostomy operation is designed to that vasal strictures and is fundementaly the same as that used in a reversal of vasectomy. The results of the surgery used to correct obstructive azoospemia are in general poor. (Jequier, 1986a).