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2.
J Pediatr Endocrinol Metab ; 32(7): 785-789, 2019 Jul 26.
Artigo em Inglês | MEDLINE | ID: mdl-31251726

RESUMO

Background Cyclic Cushing's disease (CCD) is reported to occur in approximately 15% of patients with Cushing's disease (CD). CCD is a rare phenomenon in children. Case presentation A Portuguese female with well-controlled type 1 diabetes (T1DM) on an insulin pump developed transient uncontrolled blood sugar every morning. Increased basal and bolus insulin dosing was ineffective in lowering blood sugar and she began to miss school because of nausea, vomiting, fatigue, but no ketoacidosis. Therefore, other causes of sporadic hyperglycemia were explored. Multiple 6-h urinary free cortisol (UFC) samples revealed a spike in cortisol coincident with severe hyperglycemia. Pituitary magnetic resonance imaging (MRI) revealed a 3.5 mm microadenoma and inferior petrosal sinus sampling of adrenocorticotropic hormone (ACTH) after corticotropin releasing hormone (CRH) stimulation confirmed ACTH-dependent CD. Endoscopic endonasal tumor resection led to resolution of early morning hyperglycemia and symptoms. Discussion Our case illustrates an atypical presentation of CCD. There are no previous case reports of a pediatric patient with T1DM and CCD. Unexplained hyperglycemia in a patient with previous well-controlled T1DM should prompt assessment of other causes. CCD can be easily be missed if timed 6-h UFC measurements are not obtained.


Assuntos
Diabetes Mellitus Tipo 1/complicações , Hiperglicemia/diagnóstico , Hipersecreção Hipofisária de ACTH/diagnóstico , Adolescente , Diagnóstico Diferencial , Feminino , Humanos , Hiperglicemia/etiologia , Hipersecreção Hipofisária de ACTH/etiologia , Prognóstico
3.
Eplasty ; 15: ic61, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26715949
4.
Plast Reconstr Surg ; 127(6): 2224-2231, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21617457

RESUMO

BACKGROUND: Virginal mammary hypertrophy, a rapid enlargement of one or both breasts that usually presents in the adolescent years, is a rare condition that has been reported sporadically in the medical literature. Currently, there are no patient- or disease-oriented evidence-based guidelines for the treatment of this condition. This meta-analysis examines the published case reports and presents a cumulative algorithm for the diagnosis and treatment of this uncommon condition. METHODS: A literature search was performed using PubMed, with multiple keywords. Information regarding patient age, menarchal state, mass of excision, surgical technique, number of operations, pharmacologic intervention, and recurrence was extracted from each case report and analyzed using SPSS 15.1 statistical software. RESULTS: A significant relationship was found (p < 0.01), as was an odds ratio of 7.0, for the likelihood of recurrence using a reduction mammaplasty as opposed to a mastectomy. CONCLUSIONS: Based on the evidence presented in this article, certain interventions are more effective for the treatment of virginal mammary hypertrophy. On diagnosis of virginal mammary hypertrophy, tamoxifen therapy may be considered based on previous literature, barring any medical contraindications. A subcutaneous mastectomy with complete removal of breast tissue is the procedure least likely to lead to recurrence but is more deforming. Reduction mammaplasty gives an improved aesthetic breast, but it is important to counsel the patient on the likelihood of increased recurrence. Tamoxifen therapy following surgery may decrease the recurrence rate.


Assuntos
Mama/patologia , Adolescente , Antagonistas de Estrogênios/uso terapêutico , Feminino , Humanos , Hipertrofia , Mamoplastia , Mastectomia , Recidiva , Tamoxifeno/uso terapêutico
5.
Eplasty ; 9: e6, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19221583

RESUMO

OBJECTIVE: The purpose of this review is to present the complex underlying pathophysiology that can form the basis of this common condition. METHODS: More than 20 years of clinical experience in endocrinology and plastic surgery and a review of the English-language literature were used to form the basis of this review. RESULTS: While idiopathic and physiologic causes are frequent, there are multiple, significant, underlying disorders that can result in gynecomastia, including chronic illness, cancer, medications, syndromes, and a variety of endocrinopathies. CONCLUSION: Both history and physical examination are frequently sufficient to make an appropriate diagnosis. In patients who do not have a definitive etiology of their gynecomastia, a screening battery of laboratory tests is sufficient to rule out significant pathophysiology, although these tests may be difficult to interpret in children and adolescents. An endocrinology consultation is suggested whenever an abnormal screening laboratory test occurs or if there are any other suggestions of underlying endocrinopathy.

6.
J Pediatr Endocrinol Metab ; 19(8): 1039-43, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16995590

RESUMO

A 13 year-old female with an 11-month history of type 1 diabetes mellitus (DM) was admitted to the hospital with a muscle infarction. Diagnosis of this rare complication of DM was suggested by clinical presentation, magnetic resonance imaging (MRI) and muscle biopsy. While diabetic muscle infarction (DMI) has been previously described in adult patients with long-standing DM associated with microangiopathy, it is an unexpected finding in this clinical setting.


Assuntos
Diabetes Mellitus Tipo 1/complicações , Infarto/etiologia , Músculo Esquelético/irrigação sanguínea , Adolescente , Angiopatias Diabéticas/diagnóstico , Feminino , Humanos , Infarto/diagnóstico , Imageamento por Ressonância Magnética
7.
J Assoc Nurses AIDS Care ; 13(3): 37-45, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12064020

RESUMO

Many children who are HIV infected grow poorly. An epidemiological framework guided a retrospective chart review assessing growth in three groups of children (n = 192): (a) children who were HIV infected secondary to maternal transmission (n = 77), (b) children who had been HIV-positive at birth but became seronegative and continue to be observed (seroreverters) (n = 84), and (c) HIV-infected children who had died (n = 31). Growth failure in the HIV-infected children was significantly greater than that expected in the general population. The seroreverters also demonstrated significantly more growth failure than that expected in the general population. Of the children who had linear growth failure, only 3 of 12 HIV-infected children and 2 of 11 seroreverters also had inadequate weight gain. However, 13 of 15 children with growth failure who subsequently died had poor weight gain. HIV classification was not significantly related to growth. These findings extend our understanding to a large, urban population of children in the United States including those who are older than children in other studies and who developed HIV through perinatal transmission. Nursing clinical practice and research implications are offered.


Assuntos
Crescimento , Infecções por HIV/imunologia , Infecções por HIV/fisiopatologia , Criança , Pré-Escolar , Infecções por HIV/transmissão , Humanos , Lactente , Transmissão Vertical de Doenças Infecciosas , Aumento de Peso
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