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1.
Histopathology ; 32(6): 562-5, 1998 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9675597

RESUMO

AIMS: The clinicopathological and immunohistochemical features of the second case of placental site nodule (PSN) of extrauterine, tubal location are presented. METHODS AND RESULTS: The lesion was incidentally found in the right tube during a cesarean section and eventual tubal ligation in a 23-year-old women gesta 2 para 1, after an uneventful 39-week intrauterine pregnancy. Grossly, the right Fallopian tube had a 1 cm dilatation filled by necrotic material. Microscopically, the lumen of the Fallopian tube was effaced and replaced by a rim of pleomorphic intermediate trophoblastic (IT) cells with pseudoinvasive parietal features which were positive for human placental lactogen, placental alkaline phosphatase, epithelial membrane antigen and CAM5.2. The Ki67 index was 3%. CONCLUSION: Due to its bizarre microscopic appearance, this lesion should be included in the differential diagnosis with malignant conditions. Both origins from a previous subclinical extrauterine tubal pregnancy and a possible migration of IT from a uterine implantation are considered.


Assuntos
Neoplasias das Tubas Uterinas/diagnóstico , Tumor Trofoblástico de Localização Placentária/diagnóstico , Adulto , Biomarcadores/análise , Neoplasias das Tubas Uterinas/química , Feminino , Humanos , Técnicas Imunoenzimáticas , Gravidez , Tumor Trofoblástico de Localização Placentária/química
2.
J Pediatr (Rio J) ; 71(6): 344-8, 1995.
Artigo em Português | MEDLINE | ID: mdl-14688986

RESUMO

We report the clinical history of two brothers with the classical Cockayne syndrome. The main manifestations consisted of cachectic dwarfism, mental retardation, intracranial calcifications, microcephaly, enophthalmos, senile appearance, joint hypomotility and skin photosensitivity. In one of these children, who died at 10 years of age of bronchopneumonia, necropsy studies revealed a variety of anomalies, mainly encephalic,which included an arachnoidal cyst at the base of the cerebellum, a defect apparently previously undescribed inpatients with this syndrome.

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