4 research outputs found

    The Occurrence of Uterine Benign Diseases and their Histomorphologic Characters

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    Uterine diseases are several and can develop from any part of the organ. Noticeable benign diseases are type called hydatidiform mole considered benign among gestational trophoblastic disease and is said to occur from abnormal fertilization of abnormal ova. Other forms are inflammatory, proliferative of insidious cell/tissue implant, hormonal induced, and infectious in their origin. Samples were obtained from patients consulted and admitted into Department of Morbid Anatomy of Ebonyi State University Teaching Hospital. Clinical and histopathological record books were reviewed alongside processed tissues, and slides stained by popular heamatoxylin and eosin technique in the 3 year study period. Of the 642 gynecological samples searched, result showed a progressive increase in number as the years empty from 2011 to 2013 presenting 8 uterine diseases in a population of 116 cases. A total of 518 cases were product of conception of which 250 were as a result of incomplete spontaneous abortions and 200 inappropriate criminal abortions, while 68 could not be associated with any definite cause. Leiomyoma cases were 75%, uterine/vaginal prolapsed were 6%, molar pregnancies and endometriosis 5% and while endometrial hyperplasia and uterine atrophy were 3% each and 2% each were for uterine polyp and adenomyosis in all of the 116 cases. Six age groups were involved showing that 7 diseases and total frequency of 50% occurred with age group (40-49) and is seconded by (30-39) which had 5 conditions with frequency of 21%. Attempted provisional diagnosis was based on clinical presentations, and of 116 cases 80% were confirmed accurate by laboratory diagnosis. Clinical characters of leiomyomas were the same while histomorphologic features were not entirely consistently same in all

    A country-specific FRAX model for Botswana

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    Introduction Hip fracture rates in Botswana were used to create a FRAX® model for fracture risk assessment. Objective This paper describes the development and characteristics of a country-specific FRAX model for Botswana. Methods Age-specific and sex-specific incidence of hip fracture and national mortality rates was incorporated into a FRAX model for Botswana. Ten-year fracture probabilities were compared with those from African countries having a FRAX model and African Americans from the USA. Results The probabilities of hip fracture and major osteoporotic fracture were low compared with those from South Africa (Black and Coloured) and US Blacks. Probabilities were marginally higher than for Tunisia. Conclusion The creation of a FRAX model is expected to help guide decisions about the prevention and treatment of fragility fractures in Botswana
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