Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
1.
BMC Pediatr ; 19(1): 216, 2019 07 02.
Article in English | MEDLINE | ID: mdl-31266444

ABSTRACT

BACKGROUND: Propranolol hydrochloride is the first-line agent recommended for the treatment of infantile hemangiomas (IH). Serious adverse effects of propranolol therapy for hemangiomas are infrequent. CASE PRESENTATION: We report a case presented in deep hypoglycemic coma during his treatment with propranolol for IH. Through our case report and the review of the literature, we aimed to underline the importance of recognizing adverse effects during propranolol therapy. Although propranolol has a long history of safe and effective use in infants and children, pediatricians should be aware that life-threatening adverse effects can happen during propranolol therapy for IH. CONCLUSION: Early identification of these adverse effects can be of great importance for patient management and prognosis. It must certainly be noted that not just early identification among doctors, but education for parents is crucial.


Subject(s)
Adrenergic beta-Antagonists/adverse effects , Coma/chemically induced , Hemangioma/drug therapy , Hypoglycemia/chemically induced , Propranolol/adverse effects , Administration, Oral , Adrenergic beta-Antagonists/administration & dosage , Glucose/administration & dosage , Humans , Hypoglycemia/therapy , Infant , Male , Propranolol/administration & dosage
2.
Ital J Pediatr ; 40: 35, 2014 Apr 04.
Article in English | MEDLINE | ID: mdl-24708654

ABSTRACT

Idiopathic pulmonary hemosiderosis is a rare disorder that can occur at any age and is characterized by the triad of hemoptysis, iron deficiency anemia and diffuse pulmonary infiltrates. The clinical course is exceedingly variable especially in children and a substantial proportion of this age group is undiagnosed. It is probably due to the fact that iron deficiency anemia may be the first and the only manifestation of IPH, preceding other symptoms and signs by several months and IPH is not considered as a rare cause of anemia, unless the typical triad is present. We present a case of IPH in a 13-year-old girl, treated for several months with persistent iron deficiency anemia, without response to therapy.


Subject(s)
Anemia, Iron-Deficiency/complications , Hemoglobins/metabolism , Hemosiderosis/diagnosis , Lung Diseases/diagnosis , Adolescent , Anemia, Iron-Deficiency/blood , Anemia, Iron-Deficiency/diagnosis , Diagnosis, Differential , Erythrocyte Count , Erythrocyte Indices , Female , Follow-Up Studies , Hemosiderosis/blood , Hemosiderosis/etiology , Humans , Iron/blood , Lung Diseases/blood , Lung Diseases/etiology , Tomography, X-Ray Computed , Hemosiderosis, Pulmonary
SELECTION OF CITATIONS
SEARCH DETAIL