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1.
Ghana Med J ; 57(3): 204-209, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38957679

RESUMEN

Objectives: To determine the clinical presentation, imaging features and outcomes of children with adenoid hypertrophy in our setting. Design: A retrospective study. Setting: The paediatric clinic of a private hospital in Enugu. Participants: 51 children, aged 2 to 108 months, with suggestive clinical features and radiographic report of adenoid hypertrophy who presented over 3 years. Interventions: Clinical information was obtained from the patient's medical records. Data was analysed for the clinical characteristics of the patients, the relationship between the degree of airway narrowing on a postnasal space (PNS) radiograph and treatment outcomes. Main outcome measures: Degree of airway narrowing as measured on a PNS radiograph, the type of and outcomes of treatment. Results: There was an almost equal male (54.7%): female (45.1%) ratio in the occurrence of adenoid hypertrophy, with a mean age of occurrence of 31.50 ± 3.64 months. Noisy breathing was the commonest symptom (94.1%); history of atopic rhinitis in 64.7% of cases and hyperactive airway disease in 45.1% more than 50% of cases with airway narrowing resolved with medical management only. Conclusion: Adenoid hypertrophy should be considered in evaluating the upper airway in children under five. Paediatricians should be conversant with diagnosing and managing this common cause of upper airway obstruction. Funding: None declared.


Asunto(s)
Tonsila Faríngea , Hipertrofia , Humanos , Tonsila Faríngea/patología , Tonsila Faríngea/diagnóstico por imagen , Masculino , Femenino , Nigeria , Estudios Retrospectivos , Preescolar , Niño , Lactante , Resultado del Tratamiento , Radiografía , Adenoidectomía , Instituciones de Atención Ambulatoria , Obstrucción de las Vías Aéreas/etiología , Obstrucción de las Vías Aéreas/diagnóstico por imagen , Obstrucción de las Vías Aéreas/terapia
2.
J Pediatr Endocrinol Metab ; 35(9): 1183-1188, 2022 Sep 27.
Artículo en Inglés | MEDLINE | ID: mdl-36069768

RESUMEN

OBJECTIVES: There is need to generate epidemiological data regarding paediatric endocrine disorders (PEDs) in sub-Saharan Africa, since little attention has been given endocrine disorders in children in this sub-region over the years. The aim of the study was to determine the sociodemographic characteristics of children with endocrine disorders in our paediatric endocrinology clinic, as well as the pattern of presentation of these disorders. METHODS: This study included paediatric patients who presented to the endocrine clinic over an 11-year period. Data of patients seen during the study period were retrieved from the case notes and were analyzed using SPSS version 23. RESULTS: A total of 188 patients were seen over the study period, with an almost equal male:female ratio. Five of the patients (2.7%) could not be classified into any gender because of genital ambiguity. The age of the patients at diagnosis ranged from 0 to 18 years of age with a median age of 9.03 (9.94) years. All the 14 subdivisions of paediatric endocrine disorders were documented among the patients, with thyroid disorders ranking highest among the PEDs seen. Type 1 diabetes mellitus, obesity and pubertal disorders were the most prevalent PEDs (in descending order), after thyroid disorders. Congenital hypothyroidism accounted for 14.3% of patients with thyroid disorders. CONCLUSIONS: Thyroid disorders, type 1 diabetes mellitus and obesity rank highest among the PEDs in our locality. There is the need to create awareness among healthcare workers and the general public regarding these disorders, in order to improve appropriate and timely presentation of patients to the clinic.


Asunto(s)
Diabetes Mellitus Tipo 1 , Enfermedades del Sistema Endocrino , Enfermedades de la Tiroides , Adolescente , Niño , Preescolar , Enfermedades del Sistema Endocrino/epidemiología , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Nigeria/epidemiología , Obesidad , Enfermedades de la Tiroides/diagnóstico , Enfermedades de la Tiroides/epidemiología
3.
J Med Case Rep ; 15(1): 395, 2021 Aug 09.
Artículo en Inglés | MEDLINE | ID: mdl-34365967

RESUMEN

BACKGROUND: Becker's nevus syndrome is a syndrome characterized by the presence of a Becker's nevus with ipsilateral breast hypoplasia or hypoplastic defects of the muscle, skin, or skeleton. The nevus usually consists of a circumscribed, unilateral, irregularly shaped hyperpigmented macule, commonly occurring around the anterior upper trunk, with/without hypertrichosis and/or acneiform lesions. This rare syndrome has not been reported in our locality to the best of our knowledge. CASE PRESENTATION: We report the case of a 15-year-old Igbo female patient who presented to our pediatric endocrinology clinic, University of Nigeria Teaching Hospital, Enugu, with complaints of asymmetry of the breasts and hyperpigmented macules on the side. Based on her symptoms, diagnosis of Becker's nevus syndrome was made. The diagnosis of Becker's nevus syndrome is mostly clinical, based on the presence of a Becker's nevus with ipsilateral breast hypoplasia or hypoplastic defects of the muscle, skin, or skeleton. In our patient, there was a Becker's nevus with ipsilateral breast hypoplasia. This syndrome, belonging to the class of epidermal nevus syndromes, is very rare, and is usually benign. She was placed on spironolactone tablets 50 mg daily, which have been associated with an improvement in the size of the hypoplastic breast, and her fears were allayed. CONCLUSION: This syndrome has not been reported in our locality to the best of our knowledge and, therefore, has a propensity for misdiagnosis by clinicians because of its rarity. We therefore report this to create awareness among clinicians regarding this condition that is associated with much psychosocial trauma among patients, and that can be easily managed with oral spironolactone.


Asunto(s)
Hiperpigmentación , Nevo , Neoplasias Cutáneas , Adolescente , Femenino , Humanos , Nigeria , Neoplasias Cutáneas/diagnóstico , Neoplasias Cutáneas/tratamiento farmacológico , Síndrome
4.
J Pediatr Endocrinol Metab ; 34(10): 1283-1290, 2021 Oct 26.
Artículo en Inglés | MEDLINE | ID: mdl-34271599

RESUMEN

OBJECTIVES: Despite the high prevalence of children with sickle cell anaemia (SCA) in West Africa, there is paucity of data on the height velocity and prevalence of growth failure in SCA patients. With advances in clinical care of SCA patients, could there be a spatial and secular trend in the growth pattern of these children? Hence, the compelling needs to embark on this study. The objectives of the study were to determine the prevalence of growth failure among patients with SCA and its correlation with age, gender and age at diagnosis. METHODS: A Prospective longitudinal study of a cohort of sickle cell anaemic paediatric patients from Pediatrics SCA Clinic, University of Nigeria Teaching Hospital, Ituku Ozalla. Patients were enrolled over a period of two years using a non-parametric convenient sampling method. Their heights were measured at baseline, three months, six months and at 12 months intervals and subsequently plotted on a standard WHO growth chart. The height velocities at different monthly intervals were calculated and compared with the WHO standard normal linear growth rates) for children (used as control) to identify those with GF. (i.e. <10th percentile). The main outcome measures were the mean height velocities at different months' intervals calculated and compared using the repeated measurement analysis of variance (ANOVA) and the Wilcoxon signed test. RESULTS: A cohort of 316 children aged 1-18 years with SCA was evaluated with a male preponderance of 161 (57.4%). The mean age and age at diagnosis were 11.04 ± 5.56 and 4.2 ± 1.7 years, respectively. The prevalence of growth failure and short stature was 84.7%. The burden of GF was highest among post-pubertal participants (94.1%). The most important predictor of growth velocity deficit was age (R2=0.045, standard ß coefficient = -0.22, t=-03.51, p=0.001). CONCLUSIONS: The study demonstrated high prevalence of growth failure in children and adolescents with SCA which intensified with advancement in age and older age at diagnosis.


Asunto(s)
Anemia de Células Falciformes/fisiopatología , Desarrollo Infantil/fisiología , Adolescente , Anemia de Células Falciformes/epidemiología , Estatura/fisiología , Niño , Preescolar , Estudios de Cohortes , Femenino , Humanos , Lactante , Estudios Longitudinales , Masculino , Nigeria/epidemiología , Prevalencia , Estudios Prospectivos
5.
BMC Pediatr ; 20(1): 458, 2020 10 02.
Artículo en Inglés | MEDLINE | ID: mdl-33008390

RESUMEN

BACKGROUND: There is growing concern as regards the emergence of metabolic disorders among children living with the Human Immunodeficiency Virus (HIV) worldwide. However, there is paucity of data on the correlates of metabolic indices among HIV-positive children in Africa. METHODS: This study examined 84 HIV-positive children on HAART recruited from the paediatric infectious diseases clinic of the University of Nigeria Teaching Hospital for blood glucose levels using finger-prick testing with an Accu-check glucose meter and test strips. Clinical information was obtained via clinical history and medical records. Data was analyzed to examine the relationship between FBG and the classes of HAART, duration of illness and treatment using analysis of variance (ANOVA). RESULTS: FBG was significantly associated with the classes of HAART (x2=12.4, p = 0.017). In addition, there was a significant association between FBG and duration of illness [F(2, 81) = 6.0; P = 0.004], as well as FBG and duration on HAART [F(2, 81) = 7.9; P = 0.001]. However, duration on HAART and type of HAART were the significant predictors of FBG in this study accounting for 10.5% and 4.1% of the variance, respectively. CONCLUSIONS: There is a greater risk of dysglycemia in paediatric patients with a longer cumulative exposure to HAART. Routine blood glucose checks among children on HAART, especially those who have received HAART for a longer duration of time may therefore be useful in their management.


Asunto(s)
Glucemia , Infecciones por VIH , Terapia Antirretroviral Altamente Activa/efectos adversos , Niño , Estudios Transversales , Ayuno , Infecciones por VIH/complicaciones , Infecciones por VIH/tratamiento farmacológico , Humanos , Nigeria , Prevalencia , Centros de Atención Terciaria
6.
Niger Postgrad Med J ; 27(3): 184-189, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32687117

RESUMEN

BACKGROUND: The need to generate a robust epidemiological data on the neglected tropical diseases is imperative, in order to encourage access to formal care, drive public policies and ensure the allocation of resources by policy-makers. OBJECTIVES: The objective of this study was to determine the prevalence of soil-transmitted helminthiasis (STH) and its association with nutritional variables among primary school pupils living in urban slums in a South-Eastern sub-Saharan African city of Enugu, Nigeria. METHODS: The stool samples of school-aged children living in urban slums were analyzed for ova of the helminths using the Kato-Katz methods, whereas the nutritional assessment (weight and height) was obtained and analyzed to indicate acute or chronic malnutrition. Degrees of helminthic load were then classified. The socioeconomic status was determined while the prevalence of STH and the relationship between it and the nutritional stratus was assessed to ascertain any significance between being malnourished and having STH as this will inform policy decisions. RESULTS: There were a total of 371 analyzed stool samples from 228 females (61.5%) and 143 males (38.5%), with 285 (76.8%) from the lowest socioeconomic class. The prevalence of STH was 18.1%, while that of acute and chronic malnutrition were 3.3% and 7.5%, respectively. The intensity of infestation was, however, light, with the highest mean egg intensity of 74.4 ± 32.8 documented for ascariasis. There was no statistically significant association between the presence of STH and various indices of acute and chronic malnutrition (P > 0.05). CONCLUSION: STHs prevalence is high among children living in urban slums. Nutritional status was, however, not adversely affected by helminthic infestation.


Asunto(s)
Heces/microbiología , Helmintiasis/epidemiología , Parasitosis Intestinales/epidemiología , Enfermedades Desatendidas/epidemiología , Áreas de Pobreza , Suelo/parasitología , Animales , Niño , Estudios Transversales , Femenino , Helmintiasis/diagnóstico , Humanos , Parasitosis Intestinales/parasitología , Masculino , Enfermedades Desatendidas/microbiología , Nigeria/epidemiología , Estado Nutricional , Prevalencia , Clase Social , Población Urbana
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