ABSTRACT
The authors report on a case of cylindroma of the cervix combined with a carcinoma in situ. Reviewing the literature which helped them, they studied the anatomo-pathological characteristics as well as the histogenesis and the therapy for cylindromas, which are more often found in other parts of the body. In particular, they are found in the salivary glands. There the origin is still uncertain and the evolution from the same stage is worse than in epidermoid carcinoma of the cervix.
Subject(s)
Carcinoma in Situ/pathology , Carcinoma, Adenoid Cystic/pathology , Carcinoma, Squamous Cell/pathology , Neoplasms, Multiple Primary/pathology , Uterine Cervical Neoplasms/pathology , Adult , Age Factors , Aged , Carcinoma, Adenoid Cystic/epidemiology , Carcinoma, Adenoid Cystic/therapy , Cervix Uteri/pathology , Female , Humans , Middle Aged , Prognosis , Uterine Cervical Neoplasms/epidemiology , Uterine Cervical Neoplasms/therapyABSTRACT
A cystic disease of the medulla is found in a young women at the 5th month of her first pregnancy and entails the death of the foetus in utero. The chronic renal insufficiency rapidly worsens and necessitates periodic hemodialysis. Renal transplantation is carried out from a brother with identical HLA. Two years later the graft is functioning well enough to permit another pregnancy. It proceeds without accompanying nephropathy. A caesarean operation carried out 36 weeks after amenorrhea gives birth to a girl who presents normal psychomotor development at two years of age. The authors consider the influence of pregnancy on the functioning of the kidney graft and the criteria permitting pregnancy after a renal transplant. They discuss the consequences of a renal transplant on the progress of the pregnancy and delivery. Finally, they study the effects of immunosuppressive treatment on the child in the short and long term.
Subject(s)
Kidney Transplantation , Pregnancy , Adult , Female , HumansABSTRACT
A case of epithelia malignant changes in uterine adenomyosis is reported. The adenocarcinomatous transformation in uterine adenomyosis is rare. It is necessary to identify exactly the lesion to detect several histological tests specially the integrity of endometrium. An initial phase by atypic hyperplasia and the eventual hormonal incidence are considered.
Subject(s)
Adenocarcinoma/etiology , Endometriosis/complications , Neoplasms, Multiple Primary , Uterine Neoplasms , Adenocarcinoma/pathology , Endometrial Hyperplasia/complications , Endometriosis/pathology , Female , Humans , Middle Aged , Neoplasms, Multiple Primary/pathology , Uterine Neoplasms/pathologyABSTRACT
Two sisters with multiple congenital malformations were shown to be trisomic for 10q24 to 10qter as a consequence of malsegregation of the balanced paternal translocation t(9;10) (q34;q24). Comparison of their phenotype with that of other patients reported in the literature confirms the individuality of the partial 10q trisomy syndrome.