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1.
J Pak Med Assoc ; 71(6): 1682-1685, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-34111097

RESUMO

The following is a case report of a 17-day-old female baby, born at 35 weeks' gestation, weighing 2.6 kg. She was brought to us with reluctance to feed, swelling over the left side of her face and a fever documented at 102oF, along with an erythematous, tender, localised swelling over the left pre-auricular region that measured 2 x 1.5 cm in size. Diagnostic workup and ultrasound findings were consistent with parotitis; however, her blood culture was negative. The patient was managed on antibiotics but subsequently, developed a nosocomial infection while she was admitted in the hospital, which prolonged her hospital stay to a total of 16 days. Nevertheless, she had complete resolution of the signs and symptoms on her follow-up visit. Acute parotitis should be considered in the differential diagnosis of a neonate presenting with facial swelling, reluctance to feed or incessant crying. Timely and appropriate management can result in good recovery and minimising the potential for complications.


Assuntos
Parotidite , Antibacterianos/uso terapêutico , Diagnóstico Diferencial , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Parotidite/diagnóstico , Parotidite/tratamento farmacológico
2.
J Pak Med Assoc ; 64(1): 110-4, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24605732

RESUMO

Congenital Adrenal Hyperplasia describes a group of autosomal recessive disorders characterized by a decrease in Cortisol production. 11 beta hydroxylase deficiencies is the second most common form. However, its presentation with cholestatic jaundice is extremely rare. We present a case of a 29-day-old infant who came to us with unusual dark complexion, persistent jaundice, and electrolyte imbalance. On investigation he was diagnosed as a case of congenital adrenal hyperplasia. Treatment with hydrocortisone and fludrocortisone cleared his jaundice and complexion with subsequent improvement in electrolytes. The aim of this report is to illustrate an unusual presentation of CAH with Cholestatic jaundice. This is the first case to be reported from Pakistan. The case outlines the difficult workup that was encountered in the diagnosis and management of the patient.


Assuntos
Hiperplasia Suprarrenal Congênita/complicações , Icterícia Obstrutiva/complicações , Hiperplasia Suprarrenal Congênita/diagnóstico , Humanos , Recém-Nascido , Doenças do Recém-Nascido , Icterícia Obstrutiva/fisiopatologia , Masculino
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