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1.
Magn Reson Imaging ; 17(7): 965-71, 1999 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-10463645

RESUMEN

The purpose of this paper is to describe the magnetic resonance imaging (MR) features of placenta accreta and percreta. We retrospectively reviewed MRI findings in four cases of placenta accreta/percreta to determine features which assist in identifying the presence and extent of placental implantation abnormality. All patients had ultrasound (US) examinations. Pathologic correlation was available in all cases. There were two cases of placenta percreta and two cases of placenta accreta. All cases were treated by hysterectomy. In the two cases of placenta percreta, the placenta demonstrated transmural extension through the uterus (percreta) on MRI. In the two cases of placenta accreta, the location of thinning in the uterine wall correlated with the location of placental invagination into the myometrium at pathology. US correlation was available in all four cases. Gray scale US did not demonstrate placental invasion in any of the four cases of placenta accreta/percreta, however, in two of three cases in which color Doppler was performed, there was flow at the uterine margin suspicious for implantation abnormality. In conclusion, MRI is useful for identifying the presence and extent of placenta accreta/percreta.


Asunto(s)
Imagen por Resonancia Magnética , Placenta Accreta/diagnóstico , Adulto , Femenino , Humanos , Placenta/diagnóstico por imagen , Placenta/patología , Placenta Accreta/complicaciones , Placenta Accreta/diagnóstico por imagen , Placenta Accreta/patología , Placenta Previa/complicaciones , Placenta Previa/diagnóstico , Embarazo , Estudios Retrospectivos , Ultrasonografía
2.
J Reprod Med ; 44(6): 567-70, 1999 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-10394555

RESUMEN

BACKGROUND: Ablation of the endocervical canal is sometimes performed as an adjunct to subtotal hysterectomy in an attempt to reduce mucous discharge and the risk of future neoplasia. Cystic accumulations within the canal of a partially obliterated cervical stump have not previously been reported to follow this practice. CASE REPORT: A 41-year-old woman presented with subacute cramping and cystic enlargement of the cervical stump on clinical, sonographic and magnetic resonance evaluation four years subsequent to a subtotal hysterectomy performed for menorrhagia. Cervical biopsies and cytology were benign, and vaginal trachelectomy was performed. Pathology demonstrated the fluid pocket to be a very large retention cyst (nabothian) that had occupied and distended the partially obliterated endocervical canal. CONCLUSION: Ablation of the cervical canal at subtotal hysterectomy may result in symptomatic entrapment of nabothian cysts. Internalization of the transformation zone and partial obliteration of the canal are postulated as predisposing factors.


Asunto(s)
Quistes/etiología , Histerectomía/efectos adversos , Complicaciones Posoperatorias , Enfermedades del Cuello del Útero/etiología , Adulto , Quistes/diagnóstico , Quistes/cirugía , Femenino , Humanos , Imagen por Resonancia Magnética , Ultrasonografía , Enfermedades del Cuello del Útero/diagnóstico , Enfermedades del Cuello del Útero/cirugía
3.
J Neuropathol Exp Neurol ; 57(11): 1026-34, 1998 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-9825939

RESUMEN

The neuropathologic changes in brains of very premature infants are well recognized but relatively few studies have attempted to identify if specific neuropathologic features cluster together. These data could assist in determining pathogenetic mechanisms of immature brain injury. The goal of this study is to identify which, if any, combinations of histologic features occur together. We identified the presence or absence of 19 histologic features in the brains of 67 infants from a multicenter study of 1,665 prematurely born infants whose birthweight was 500-1,500 grams. We used clustering algorithms and factor analysis to group pathologic features that occurred together. Our results indicate that certain histopathologic features do cluster. For example, telencephalic white matter astrocytosis occurs in 2 groups: 1) associated with amphophilic globules, and, 2) in an uncorrelated group, associated with focal macrophage deposits and coagulative necroses. Parenchymal hemorrhage was not found to be associated with any telencephalic leukoencephalopathy, regardless of whether characterized by rarefaction, astrocytosis, focal coagulative necroses, or foci of macrophages in the white matter. Intraventricular hemorrhage and germinal matrix hemorrhage were not seen together more often than by chance expectation. Intraventricular hemorrhage was only marginally associated with parenchymal hemorrhage. Our data indicate that specific histopathologic features tend to preferentially cluster with each other in groups. This clustering may represent the manifestation of a common mechanism for each. These data should be valuable indicators for future research attempting to establish pathogenesis.


Asunto(s)
Encéfalo/patología , Recién Nacido de Bajo Peso , Algoritmos , Astrocitos/patología , Encefalopatías/patología , Hemorragia Cerebral/patología , Análisis por Conglomerados , Análisis Factorial , Edad Gestacional , Humanos , Recién Nacido , Macrófagos/patología , Análisis de Supervivencia
4.
Ment Retard ; 33(2): 84-9, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-7760729

RESUMEN

The prevalence of intestinal parasite infection among program participants of the New York State Office of Mental Retardation and Developmental Disabilities for the period 1986-1987 was estimated, and demographic factors associated with increased risk for infection were identified. The overall prevalence of infection was 7.3%. The two most prevalent infections were Enterobius vermicularis (4.5%) and strongyloides stercoralis (1.2%). Males and individuals with severe or profound mental retardation were twice as likely to be positive for the presence of intestinal parasites as females and individuals with mild/moderate retardation. The relatively low prevalence found in this study compared with previous surveys suggests that management of parasitic infection is improving in conjunction with developments in delivery of medical and habilitative services.


Asunto(s)
Discapacidad Intelectual/epidemiología , Parasitosis Intestinales/epidemiología , Adolescente , Adulto , Anciano , Estudios Transversales , Evaluación de la Discapacidad , Enterobiasis/complicaciones , Enterobiasis/epidemiología , Femenino , Humanos , Incidencia , Discapacidad Intelectual/complicaciones , Parasitosis Intestinales/complicaciones , Masculino , Tamizaje Masivo , Persona de Mediana Edad , New York/epidemiología , Factores de Riesgo , Estrongiloidiasis/complicaciones , Estrongiloidiasis/epidemiología
5.
Neurology ; 42(1): 149-56, 1992 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-1346470

RESUMEN

The "modified host protein" model of scrapie proposes that the transmissible agent is composed of the degradation-resistant protein, Sp33-37, and that clinical and pathologic signs result from neurotoxic accumulations of this protein. Sp33-37 is an abnormal, amyloidogenic isoform of the normally occurring cellular protein Cp33-37. This study investigated the tissue distribution of Cp33-37 in hamster. In brain, Cp33-37 was most concentrated in the hippocampal formation. Immunohistochemical studies localized Cp33-37 to neurons and surrounding neuropil in hippocampus; septal, caudate, and thalamic nuclei; dorsal root ganglia cells; and large-diameter dorsal root axons. In non-neuronal hamster tissues, Cp33-37 was detected in circulating leukocytes, heart, skeletal muscle, lung, intestinal tract, spleen, testis, ovary, and some other organs. The presence of Cp33-37 in extracerebral tissues indicates that its function is not unique to brain. These results indicate that the molecular substrate for the production of Sp33-37, the scrapie agent, and scrapie amyloid is present in a variety of cerebral and extracerebral sites.


Asunto(s)
Priones/metabolismo , Animales , Encéfalo/metabolismo , Cricetinae , Mucosa Gástrica/metabolismo , Inmunohistoquímica , Pulmón/citología , Pulmón/metabolismo , Pulmón/ultraestructura , Microscopía Inmunoelectrónica , Proteínas PrPSc , Médula Espinal/citología , Médula Espinal/metabolismo , Estómago/citología , Distribución Tisular
6.
Am J Med Genet ; 41(3): 289-94, 1991 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-1724112

RESUMEN

Fragile X [fraX] syndrome is a common hereditary disorder associated with a fragile site marker at Xq27.3 which clinically presents as a form of mental retardation (MR). Postmortem investigation of 3 fraX positive males with mild to moderate MR did not document any gross neuropathological changes. Golgi analysis of neocortical dendritic spine morphology extended our previous observations of immature, long, tortuous spines in one adult case of fraX (Rudelli, et al., Acta Neuropathologica 67:289-295, 1985) to 2 new cases. Evidence for similar dendritic spine abnormalities was found, although Golgi analysis was less than optimal because of incomplete dendritic stain impregnation. Neocortical intra-layer cell density was also investigated in all 3 cases. Cresyl violet stained neurons were counted in 10 randomly selected fields in neocortical layers II-VI of cingulate and temporal association areas (Brodmann's areas 23 and 38). Neuron counts in fraX and control neocortex showed no significant differences. Thus, abnormal dendritic spine morphology with preservation of neuronal density appears to characterize the neocortex in individuals with this common form of mental retardation.


Asunto(s)
Corteza Cerebral/patología , Síndrome del Cromosoma X Frágil/patología , Adolescente , Adulto , Análisis de Varianza , Recuento de Células , Humanos , Discapacidad Intelectual/genética , Discapacidad Intelectual/patología , Cariotipificación , Masculino , Persona de Mediana Edad , Neuronas/citología , Linaje , Coloración y Etiquetado
7.
J Gen Virol ; 72 ( Pt 12): 2905-13, 1991 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-1684986

RESUMEN

Studies were conducted to determine whether accumulation of the scrapie agent protein Sp33-37 in brain correlated with the appearance of the scrapie agent or with pathology. The concentrations of the scrapie agent and Sp33-37 were measured in purified fraction P5 isolated from hamster brains at weekly intervals after inoculation. The scrapie agent concentration in fraction P5 was approximately 10(-1) LD50/g brain 1 day post-inoculation and increased to 10(9.4) LD50/g at day 77. Sp33-37 was first detected in P5 at day 21, when the agent titre was 10(3.9) LD50/g. Sp33-37 concentration increased in concert with the scrapie agent concentration, although the apparent rate of increase was somewhat lower for the protein than for the agent. The histopathological evidence of disease, consisting of mild vacuolation and gliosis, was first seen at 35 days, but was not conspicuous until 49 to 56 days post-inoculation. Vacuolation and gliosis increased until termination of the experiment at day 77. Amyloid plaques were first detected at 56 days and were widespread at day 77. Clinical disease was first seen in these animals at day 66, with an average onset at day 71. Control animals inoculated with buffer alone showed some mild gliosis, but were otherwise normal. The fact that Sp33-37 purified with the scrapie agent isolated from brain 14 days prior to detectable (light microscopic) pathology supports the theory that Sp33-37 is the major structural component of the scrapie agent and not solely a product of the pathology.


Asunto(s)
Encéfalo/microbiología , Priones/aislamiento & purificación , Scrapie/patología , Animales , Western Blotting , Encéfalo/metabolismo , Cricetinae , Electroforesis en Gel de Poliacrilamida , Femenino , Proteínas PrPSc , Scrapie/metabolismo
8.
Am J Med Genet ; 38(2-3): 476-80, 1991.
Artículo en Inglés | MEDLINE | ID: mdl-2018089

RESUMEN

We have evaluated 62 fragile X syndrome [fra(X)] individuals (55 males and 7 females) with different degrees of developmental disabilities that were clinically non-progressive and non-focal in character. The mean age for the 55 males was 23.1 years +/- 14.3 SD with a range of 2-70: for the 7 females, the mean age was 15.7 years +/- 3.5 SD with a range of 10-20 years. Mental retardation (MR) was found in 53 males (8/53 [15.1%] mild, 26/53 [49.1%] moderate, 14/53 [26.4%] severe, and 5/53 [9.4%] profound). Learning disabilities were found in 2/55 (3.6%) of males. One of the 7 females had mild and one had moderate MR: the other 5 were learning disabled. Autistic stigmata were present in 10/62 (16%) of the patients. Only 14/62 (23%) had a history of seizures, all of which were controlled with anticonvulsants. In 36/62 cases, an electroencephalogram (EEG) was performed. We compared these data with that of others. Brain stem auditory evoked response (BAER) was performed in 12 cases. Abnormalities were found in only 5/12. Neuroimaging and computerized cranial transaxial tomography (CT scan) were performed on 21/62 (34%) of the patients. Only 8 of these 21 (38%) studies were abnormal. One patient died; neuropathological studies showed mild brain atrophy, with light microscopic and ultrastructural abnormalities. Rapid Golgi dendritic spine patterns showed that the proximal apical segments were abnormally developed. Very thin, long tortuous spines with prominent terminal heads and irregular dilatations were present. Marked reductions in the length of the synapses, as determined on EPTA-postfixed tissue where noted.(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Síndrome del Cromosoma X Frágil/fisiopatología , Adolescente , Adulto , Anciano , Trastorno Autístico/genética , Trastorno Autístico/fisiopatología , Encéfalo/patología , Niño , Preescolar , Electroencefalografía , Femenino , Humanos , Discapacidad Intelectual/genética , Discapacidad Intelectual/fisiopatología , Discapacidades para el Aprendizaje/genética , Discapacidades para el Aprendizaje/fisiopatología , Masculino , Persona de Mediana Edad , Hipotonía Muscular/genética , Hipotonía Muscular/fisiopatología , Convulsiones/genética , Convulsiones/fisiopatología
9.
Life Sci ; 48(7): 693-701, 1991.
Artículo en Inglés | MEDLINE | ID: mdl-1990239

RESUMEN

As part of an ongoing biochemical study in nutrition we examined blood profiles, serum chemistry, lymphocyte transformation and lymphoid pathology in cats fed a diet containing 5% cystine with and without taurine. Automated blood counts of whole blood samples showed a decrease in red blood cell counts accompanied by a significant decrease in hemoglobin and hematocrit in cats fed 5% cystine in the absence of taurine compared to cats fed 0.05% taurine (control). A significant increase was noted in serum cholesterol in cats fed cystine and cystine/taurine compared to cats fed control diets. There were no significant differences in lymphocyte transformation using leukocytes isolated from the spleen and blood with the mitogens, phytohemagglutinin and pokeweed. However, lymphocyte transformation of both spleen and blood without mitogen from the excess cystine group were significantly higher than leukocytes from the 0.05% taurine group (control). Pathological examination of regional lymph nodes, livers, and spleens showed histological abnormalities in cats fed the excess cystine diet. These results indicate that there are alterations in the immune system of cats fed a diet containing 5% cystine with and without dietary taurine.


Asunto(s)
Cistina/farmacología , Dieta , Sistema Inmunológico/efectos de los fármacos , Activación de Linfocitos/efectos de los fármacos , Taurina/farmacología , Animales , Gatos , Cistina/toxicidad , Recuento de Eritrocitos/efectos de los fármacos , Femenino , Hematócrito , Hemoglobinas/análisis , Recuento de Leucocitos/efectos de los fármacos , Ganglios Linfáticos/efectos de los fármacos , Ganglios Linfáticos/patología , Bazo/efectos de los fármacos , Bazo/patología
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