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1.
Avian Dis ; 41(2): 469-71, 1997.
Article in English | MEDLINE | ID: mdl-9201417

ABSTRACT

The finding of closely associated squamous cell carcinoma (SCC)-like lesions and pox lesions in chorioallantoic membranes (CAMs) inoculated with skin and palate samples taken from broilers is described. The samples were obtained from two broilers coming from different flocks that were not vaccinated against fowl pox. Both birds presented skin lesions, which were diagnosed in one bird as fowl pox, and in the other as SCC. After inoculation of CAMs with fresh tissues from both birds, histologic examination revealed, in all CAMs, lesions that were characteristic of fowl pox together with lesions consistent with those seen in the skin of broilers affected with SCC. This finding was unexpected and may shed some light on the etiology of SCC.


Subject(s)
Carcinoma, Squamous Cell/veterinary , Chick Embryo/pathology , Fowlpox/pathology , Palatal Neoplasms/veterinary , Poultry Diseases , Skin Neoplasms/veterinary , Allantois/pathology , Animals , Carcinoma, Squamous Cell/embryology , Carcinoma, Squamous Cell/pathology , Chickens , Chorion/pathology , Epithelium/pathology , Fowlpox/embryology , Palatal Neoplasms/embryology , Palatal Neoplasms/pathology , Skin Neoplasms/embryology , Skin Neoplasms/pathology
2.
Teratology ; 46(4): 399-404, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1384156

ABSTRACT

A 40-year-old white woman underwent amniocentesis for advanced maternal age at 15.4 weeks gestation. Fetal chromosome analysis demonstrated two distinct cell lines: [46,XX,t(1;19)(p11;p11)]--10%; and [47,XX,t(1;19)(p11;p11) + der(1)t(1;19)(p11;q11)]--90%. The latter karyotype was trisomic for both 1q and 19p. The mother carried the balanced translocation; the father had a normal karyotype. Amniotic fluid alpha-fetoprotein level was elevated and an acetylcholinesterase band was detected. Level II ultrasonography at 17 and 24 weeks revealed several abnormalities, including a large facial cleft and a probable facial teratoma and intracranial tumor. Autopsy following pregnancy termination confirmed the presence of both. Chromosome evaluation of 172 metaphases of both the epignathus and the intracranial teratoma demonstrated a predominance of the cell line with 47 chromosomes (166/172 = 96.5%), while from nonteratoma tissue (lung, liver, skin, and brain) only the balanced karyotype was detected. These observations suggest that the chromosomal imbalance is instrumental in the etiology of the teratoma.


Subject(s)
Abnormalities, Multiple/genetics , Amniocentesis , Chromosome Aberrations/genetics , Chromosomes, Human, Pair 19/ultrastructure , Chromosomes, Human, Pair 1/ultrastructure , Fetal Diseases/diagnosis , Mosaicism , Neoplasms, Multiple Primary/embryology , Palatal Neoplasms/embryology , Skull Neoplasms/embryology , Teratoma/embryology , Trisomy , Abortion, Therapeutic , Adult , Chromosome Aberrations/pathology , Chromosome Disorders , Female , Fetal Diseases/diagnostic imaging , Fetal Diseases/genetics , Humans , Neoplasms, Multiple Primary/genetics , Palatal Neoplasms/genetics , Skull Neoplasms/genetics , Teratoma/genetics , Ultrasonography , alpha-Fetoproteins/analysis
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