“Paciente masculino de 6 años de edad con anemia falciforme”
Sickle cell anemia, sickle cell anemia or sickle cell disease, is a pathology of frequent genetic origin in which the inheritance of two mutant genes of hemoglobin, the present clinical case aims to analyze the procedures of the techniques applied for the diagnosis of sickle cell anemia in a boy of...
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| Format: | bachelorThesis |
| Language: | spa |
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2018
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| Online Access: | http://dspace.utb.edu.ec/handle/49000/4951 |
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| author | Pasos Baño, Frank Rodrigo |
| author_facet | Pasos Baño, Frank Rodrigo |
| author_role | author |
| collection | Repositorio Universidad Técnica de Babahoyo |
| dc.contributor.none.fl_str_mv | Salazar Carranza, Luz Angélica |
| dc.creator.none.fl_str_mv | Pasos Baño, Frank Rodrigo |
| dc.date.none.fl_str_mv | 2018-12-06T20:18:27Z 2018-12-06T20:18:27Z 2018 |
| dc.format.none.fl_str_mv | Pag, 36 application/pdf |
| dc.identifier.none.fl_str_mv | http://dspace.utb.edu.ec/handle/49000/4951 |
| dc.language.none.fl_str_mv | spa |
| dc.publisher.none.fl_str_mv | BABAHOYO, UTB 2018 |
| dc.rights.none.fl_str_mv | http://creativecommons.org/licenses/by-nc-sa/3.0/ec/ info:eu-repo/semantics/openAccess |
| dc.source.none.fl_str_mv | reponame:Repositorio Universidad Técnica de Babahoyo instname:Universidad Técnica de Babahoyo instacron:UTB |
| dc.subject.none.fl_str_mv | Anemia de Células Falciformes Anemia Drepanocítica |
| dc.title.none.fl_str_mv | “Paciente masculino de 6 años de edad con anemia falciforme” |
| dc.type.none.fl_str_mv | info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/bachelorThesis |
| description | Sickle cell anemia, sickle cell anemia or sickle cell disease, is a pathology of frequent genetic origin in which the inheritance of two mutant genes of hemoglobin, the present clinical case aims to analyze the procedures of the techniques applied for the diagnosis of sickle cell anemia in a boy of 6 years of age, male, Afro Ecuadorian, with a personal history of asthma, fracture of the left femur, chronic constipation, presents a clinical picture of abdominal pain type colic, associated with vomiting of bilious content, which is performed a complete blood count with the following results: Hemogram: Hemoglobin: 9.6; Hematocrit: 28.3% Average Corpuscular Volume: 88.6; HCM: 30.1; Platelets: 517,000; Leukocytes: 15,800 (Neutrophils: 92.6% lymphocytes: 5.9%) Biochemistry: Sodium: 131.9; Potassium: 4.07; Urea: 13.2; Creatinine 0.4; Glucose: 120; LDH: 696; TGO: 59; TGP: 47; TGG: 59; Total bilirubin: 2. Basal gasometry: pH: 7,469; pO2: 58; PCO2: 35; HCO3: 25.6; O2 saturation: 91.5%. Upon suspicion of sickle cell anemia, a blood smear was performed, which showed the presence of sickle-shaped red blood cells. Once the disease is diagnosed, a conservative treatment is applied to the associated pathologies, pain management. |
| eu_rights_str_mv | openAccess |
| format | bachelorThesis |
| id | UTB_97ea61f6efd6302e9a986272efdacff5 |
| instacron_str | UTB |
| institution | UTB |
| instname_str | Universidad Técnica de Babahoyo |
| language | spa |
| network_acronym_str | UTB |
| network_name_str | Repositorio Universidad Técnica de Babahoyo |
| oai_identifier_str | oai:dspace.utb.edu.ec:49000/4951 |
| publishDate | 2018 |
| publisher.none.fl_str_mv | BABAHOYO, UTB 2018 |
| reponame_str | Repositorio Universidad Técnica de Babahoyo |
| repository.mail.fl_str_mv | . |
| repository.name.fl_str_mv | Repositorio Universidad Técnica de Babahoyo - Universidad Técnica de Babahoyo |
| repository_id_str | 0 |
| rights_invalid_str_mv | http://creativecommons.org/licenses/by-nc-sa/3.0/ec/ |
| spelling | “Paciente masculino de 6 años de edad con anemia falciforme”Pasos Baño, Frank RodrigoAnemia de Células FalciformesAnemia DrepanocíticaSickle cell anemia, sickle cell anemia or sickle cell disease, is a pathology of frequent genetic origin in which the inheritance of two mutant genes of hemoglobin, the present clinical case aims to analyze the procedures of the techniques applied for the diagnosis of sickle cell anemia in a boy of 6 years of age, male, Afro Ecuadorian, with a personal history of asthma, fracture of the left femur, chronic constipation, presents a clinical picture of abdominal pain type colic, associated with vomiting of bilious content, which is performed a complete blood count with the following results: Hemogram: Hemoglobin: 9.6; Hematocrit: 28.3% Average Corpuscular Volume: 88.6; HCM: 30.1; Platelets: 517,000; Leukocytes: 15,800 (Neutrophils: 92.6% lymphocytes: 5.9%) Biochemistry: Sodium: 131.9; Potassium: 4.07; Urea: 13.2; Creatinine 0.4; Glucose: 120; LDH: 696; TGO: 59; TGP: 47; TGG: 59; Total bilirubin: 2. Basal gasometry: pH: 7,469; pO2: 58; PCO2: 35; HCO3: 25.6; O2 saturation: 91.5%. Upon suspicion of sickle cell anemia, a blood smear was performed, which showed the presence of sickle-shaped red blood cells. Once the disease is diagnosed, a conservative treatment is applied to the associated pathologies, pain management.Anemia de células falciformes, anemia drepanocítica o drepanocitosis, es una patología de origen genético frecuente en que la herencia de dos genes mutantes de la hemoglobina, el presente caso clínico tiene por objetivo analizar los procedimientos de las técnicas aplicadas para el diagnóstico de Anemia Falciforme en un niño de 6 años de edad, de sexo masculino, afro ecuatoriano, con antecedentes personales de asma, fractura de fémur izquierdo, estreñimiento crónico, presenta un cuadro clínico de dolor abdominal tipo cólico, asociado a vómitos de contenido bilioso, al que se le realizó una biometría hemática completa obteniendo como resultados: Hemograma: Hemoglobina: 9,6; Hematocrito: 28,3% Volumen Corpuscular Medio: 88,6; HCM: 30,1; Plaquetas: 517.000; Leucocitos: 15.800 (Neutrofilos: 92,6% linfocitos: 5,9%) Bioquímica: Sodio: 131,9; Potasio: 4,07; Urea: 13,2; Creatinina 0,4; Glucosa: 120; LDH: 696; TGO: 59; TGP: 47; TGG: 59; Bilirrubina total: 2. Gasometría basal: pH: 7,469; pO2: 58; PCO2: 35; HCO3: 25,6; Saturación O2: 91,5%. Ante la sospecha de Anemia Falciforme se realizó frotis sanguíneo que evidencio la presencia de glóbulos rojos en forma de Hoz. Una vez diagnosticada la enfermedad se le realiza un tratamiento conservador a las patologías asociadas, manejo del dolor.BABAHOYO, UTB 2018Salazar Carranza, Luz Angélica2018-12-06T20:18:27Z2018-12-06T20:18:27Z2018info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bachelorThesisPag, 36application/pdfhttp://dspace.utb.edu.ec/handle/49000/4951spahttp://creativecommons.org/licenses/by-nc-sa/3.0/ec/info:eu-repo/semantics/openAccessreponame:Repositorio Universidad Técnica de Babahoyoinstname:Universidad Técnica de Babahoyoinstacron:UTB2018-12-07T08:00:31Zoai:dspace.utb.edu.ec:49000/4951Institucionalhttp://dspace.utb.edu.ec/Universidad públicahttps://utb.edu.ec/http://dspace.utb.edu.ec/oai.Ecuador...opendoar:02026-04-25T22:23:33.502762Repositorio Universidad Técnica de Babahoyo - Universidad Técnica de Babahoyotrue |
| spellingShingle | “Paciente masculino de 6 años de edad con anemia falciforme” Pasos Baño, Frank Rodrigo Anemia de Células Falciformes Anemia Drepanocítica |
| status_str | publishedVersion |
| title | “Paciente masculino de 6 años de edad con anemia falciforme” |
| title_full | “Paciente masculino de 6 años de edad con anemia falciforme” |
| title_fullStr | “Paciente masculino de 6 años de edad con anemia falciforme” |
| title_full_unstemmed | “Paciente masculino de 6 años de edad con anemia falciforme” |
| title_short | “Paciente masculino de 6 años de edad con anemia falciforme” |
| title_sort | “Paciente masculino de 6 años de edad con anemia falciforme” |
| topic | Anemia de Células Falciformes Anemia Drepanocítica |
| url | http://dspace.utb.edu.ec/handle/49000/4951 |