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1.
Braz. j. infect. dis ; 6(2): 97-99, Apr. 2002.
Article in English | LILACS, SES-SP | ID: lil-332303

ABSTRACT

We describe the pathology of a unique case of Fallopian tube amebiasis, associated with hydrosalpinx, in a 21-year-old woman. She complained of lower abdominal pain, had a foul-smelling green vaginal discharge and fever during one week. There was a discrete increase in body temperature and a painful abdominal palpation at the lower right side, with signs of local peritoneal irritation. Pathological examination showed a marked dilatation of the fallopian tube and hydrosalpinx. Microscopic examination showed a poorly formed granuloma composed of large macrophages with many Entamoeba histolytica trophozoites inside the fallopian tube. Even though it is a rare disease the correct diagnosis of female genital tract amebiasis is of great importance for the indication of proper therapy.


Subject(s)
Adult , Animals , Female , Humans , Salpingitis , Entamoeba histolytica , Entamoebiasis/diagnosis , Entamoebiasis/parasitology , Salpingitis , Fallopian Tubes , Entamoebiasis/surgery
2.
Arq. neuropsiquiatr ; 42(2): 146-51, 1984.
Article in Portuguese | LILACS | ID: lil-20516

ABSTRACT

Miastenia grave e doenca neuromuscular caracterizada por excessiva fatigabilidade da juncao muscular e envolve, particularmente, musculos inervados por nervos cranianos. Acredita-se que o defeito esteja localizado na juncao neuromuscular. Os autores estudaram os achados histoquimicos e morfometricos em 4 pacientes com miastenia grave mostrando que as fibras do tipo II eram significativamente menores que as fibras do tipo I


Subject(s)
Adolescent , Adult , Middle Aged , Humans , Male , Female , Muscles , Myasthenia Gravis , Nerve Fibers , Biopsy , Coloring Agents
4.
Arq. neuropsiquiatr ; 41(3): 292-308, 1983.
Article in Portuguese | LILACS | ID: lil-14066

ABSTRACT

Estudamos um paciente com quadro clinico rebelde, produzido por intoxicacao pelo parathion. Foi observado um fenomeno miotonico transitorio, nao descrito na literatura revisada. A constatacao de cifras de AchE eritrocitaria baixas e de colinesterase plasmatica normais, indicou que era portador de deficit congenito de AchE, esclarecendo-se a evolucao cronica do seu quadro. O fenomeno miotonico associado ao quadro clinico, eletrofisiologico, histologico e bioquimico fazem deste paciente um modelo clinico, de etiologia conhecida, da discutida sindrome de Isaacs


Subject(s)
Adult , Humans , Male , Cholinesterases , Neuromuscular Diseases , Parathion
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