RESUMO
O objetivo deste trabalho foi realizar um levantamento casuístico de diagnósticos de Hepatozoon durante 2018 e 2019, enfatizando os aspectos hematológicos de maior incidência relacionados aos animais e a sazonalidade. A pesquisa foi realizada no Laboratório de Patologia Clínica do Hospital Veterinário do Instituto Federal da Paraíba e em um laboratório veterinário particular, localizado no município de Sousa/PB. Os dados foram obtidos através de uma avaliação retrospectiva de hemogramas realizados em 718 amostras de cães, provenientes da zona urbana e diagnosticados para Hepatozoon spp. Verificou-se que 35 (4,8%) cães foram positivos, a partir da visualização de gamontes parasitando neutrófilos. Dentre esses animais infectados, 16 (45%) eram fêmeas e 19 (55%) eram machos. Em relação à idade, houve predominância em animais jovens com até três anos, totalizando 25 (72%) animais. A infecção natural por Hepatozoon spp. foi superior na estação mais seca, entre os meses de janeiro e maio. Os aspectos hematológicos foram variáveis nos animais infectados, onde os mais observados foram: anemia em 23 (65%); trombocitopenia em 14 (40%); leucocitose por neutrofilia em 11 (31%) e hiperproteinemia em 11 (31%) dos animais. Conclui-se que a prevalência da infecção por Hepatozoon spp. foi de 4,8% em cães na região urbana do Sertão Paraíbano, destacando-se o período dos meses mais quentes, com ocorrência maior em cães sem raça definida (SRD), sem predileção por sexo e idade. Os achados hematológicos entre os animais infectados foram variáveis, com maior frequência de anemia, trombocitopenia, leucocitose e hiperproteinemia.
This study aimed to conduct a case-by-case survey of diagnosed cases of Hepatozoon during in the period from 2018 - 2019, emphasizing the hematological aspects of higher incidence related to the animals and the seasonality. The research was carried out at the Clinical Pathology Laboratory of the Veterinary Hospital of the Federal Institute of Paraíba, and at a private Veterinary Laboratory located in the city of Sousa/PB. Data were obtained through a retrospective evaluation of blood counts performed in 718 samples of dogs from urban areas and diagnosed for Hepatozoon spp. It was found that 35 (4.8%) dogs were positive, from the visualization of gamontes parasitizing neutrophils. Among these infected animals, 16 (45%) were female and 19 (55%) were males. Regarding the age, there was a predominance in young animals up to 3 years old, totalizing 25 (72%) animals. The natural infection by Hepatozoon spp. was higher in the driest season, from January to May. The hematological aspects were variable in the infected animals, where the most observed were: anemia 23 (65%), thrombocytopenia 14 (40%), leukocytosis by neutrophilia 11 (31%), and hyperproteinemia 11 (31%). It is concluded that the prevalence of infection by Hepatozoon spp. was 4.8% in dogs in the urban region of Sertão Paraíbano, highlighting the period of warmer months, with a greater occurrence in mixed breed dogs (SRD), with no predilection for sex and age. The hematological findings among the infected animals were variable, with a higher frequency of anemia, thrombocytopenia, leukocytosis, and hyperproteinemia.
Assuntos
Animais , Cães , Trombocitopenia/veterinária , Transtornos das Proteínas Sanguíneas/veterinária , Eucoccidiida , Coccidiose/patologia , Anemia/veterinária , Leucocitose/veterinária , Contagem de Células Sanguíneas/veterináriaRESUMO
The activated protein C resistance (APC-R) ratios in 50 patients with steady state homozygous sickle cell (SS) disease and 59 healthy AA controls was measured. There was a significant reduction in median APC-R ratio in sickle cell disease compared to controls. This reduction in APC-R ratio was not explained by (1) the presence of the factor V Leiden, found in only one of 165 patients with SS disease including those tested for APC-R, or (2) the presence of lupus anticoagulants. However, the raised levels of factor VIIIC in SS patients in this study may be contributing to increased resistance to APC, which in turn may contribute to the vaso-occlusive complications of SS disease.
Assuntos
Anemia Falciforme/sangue , Transtornos das Proteínas Sanguíneas/sangue , Proteína C , Adolescente , Adulto , Anemia Falciforme/complicações , Anemia Falciforme/genética , Transtornos da Coagulação Sanguínea/sangue , Transtornos da Coagulação Sanguínea/complicações , Transtornos das Proteínas Sanguíneas/complicações , Feminino , Homozigoto , Humanos , Masculino , Tempo de ProtrombinaRESUMO
The activated protein C resistance (APC-R) ratios in 50 patients with steady state homozygous sickle cell (SS) disease and 59 healthy AA controls was measured. There was a significant reduction in median APC-R ratio in sickle cell disease compared to controls. This reduction in APC-R ratio was not explained by (1) the presence of the factor V Leiden, found in only one of 165 patients with SS disease including those tested for APC-R, or (2) the presence of lupus anticoagulants. However, the raised levels of factor VIIIC in SS patients in this study may be contributing to the increased resistance to APC, which in turn may contribute to the vaso-occlusive complication of SS disease.(AU)
Assuntos
Adolescente , Adulto , Feminino , Humanos , Masculino , Anemia Falciforme/sangue , Transtornos das Proteínas Sanguíneas/sangue , Proteína C , Anemia Falciforme/complicações , Anemia Falciforme/genética , Transtornos da Coagulação Sanguínea/sangue , Transtornos da Coagulação Sanguínea/complicações , Transtornos das Proteínas Sanguíneas/complicações , Homozigoto , Tempo de ProtrombinaRESUMO
A 4-month-old girl who was examined because of splenomegaly had portal vein thrombosis, which apparently resulted from a combination of cytomegalovirus infection and deficiency of both protein S and protein C. The cytomegalovirus infection, by damaging endothelial cells, may have triggered a cascade of events that was ultimately expressed as portal vein thrombosis resulting from deficiency of proteins S and C.
Assuntos
Transtornos das Proteínas Sanguíneas/complicações , Infecções por Citomegalovirus/complicações , Veia Porta , Deficiência de Proteína C , Deficiência de Proteína S/complicações , Trombose/etiologia , Feminino , Humanos , LactenteRESUMO
We present one case of hereditary bisalbuminuria and bisalbuminemia in a Spanish family with three affected members. The double band of albumin was detected accidentally in an routine analytical study of a patient who showed hyperuricemia, this originated the study of the rest of the members of the family. Protein electrophoresis, in serum as well as in urine, showed a double band of albumin, which as in most published cases corresponded to the slow migration type. With immunoelectrophoresis its immune identity with common albumin was established. The biochemical parameters assessed did not show any alteration which could correlate the protein disorder with any associated pathology.
Assuntos
Albuminas/análise , Albuminúria/genética , Transtornos das Proteínas Sanguíneas/genética , Adulto , Eletroforese , Feminino , Humanos , Imunoeletroforese , Masculino , LinhagemRESUMO
Description of the first case of angio-immunoblastic lymphadenopathy with dysproteinemia diagnosed in a male patient 64 years old and which preceded the development of a lymphoma. The importance of this study is the association that may exist between certain drugs and the development of angioimmunoblastic lymphadenopathy, which occurred in our patient with the use of diphenylhydantoin. This disease can present itself up to 22 years after exposure to the agent.