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5.
BMJ Case Rep ; 2009: bcr2008139014, 2009.
Article in English | MEDLINE | ID: mdl-21687321
13.
Indian J Pediatr ; 71(10): 948, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15531851

ABSTRACT

A girl presented with a dull ache in the neck and mild difficulty in neck movements. She had limited clinical signs and her initial work up failed to reveal the cause. With the help of imaging modalities and CT guided needle biopsy, she was diagnosed to have an eosinophilic granuloma of the fifth cervical vertebra. There were no neurological symptoms. She was successfully managed with immobilization of spine, local irradiation and systemic vinblastine. The literature is briefly reviewed for clinical features, diagnosis and management.


Subject(s)
Cervical Vertebrae , Dancing , Eosinophilic Granuloma/diagnosis , Neck Pain/etiology , Child , Combined Modality Therapy , Eosinophilic Granuloma/complications , Eosinophilic Granuloma/therapy , Female , Humans , Movement/physiology , Neck/physiology
14.
Indian J Pediatr ; 71(8): 751-3, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15345879

ABSTRACT

Jugular phlebectasia is a rare cause of cervical swelling in children. It is a fusiform dilatation of any part of the jugular venous system and can involve the external, internal or anterior jugular veins. Previous reports suggest that the entity is often ignored or misdiagnosed. Unilateral internal jugular phlebactasia presenting as an intermittent neck swelling in a ten-year-old girl is reported. The clinical features are analyzed and the appropriate use of noninvasive imaging modalities is highlighted. The literature is also briefly reviewed.


Subject(s)
Jugular Veins/pathology , Child , Dilatation, Pathologic/diagnostic imaging , Female , Humans , Jugular Veins/diagnostic imaging , Ultrasonography, Doppler, Color , Valsalva Maneuver
15.
East Afr Med J ; 81(1): 59-60, 2004 Jan.
Article in English | MEDLINE | ID: mdl-15080519

ABSTRACT

Beckwith-Wiedemann syndrome is the most common overgrowth malformation syndrome. The classical features include macrosomia, macroglossia, omphalocele and ear lobe anomalies. Among the associated adrenal anomalies, foetal cortical cytomegaly, outer cortical haemorrhage and unilateral benign cysts are well described. A term neonate was admitted with typical features of the syndrome. Radiological evaluation revealed a rare association of bilateral benign hamorrhagic adrenal cysts. Serial sonography confirmed hamorrhage into benign cysts and ruled out neoplasms. Only one similar case has been documented in the literature previously.


Subject(s)
Adrenal Gland Diseases/diagnostic imaging , Beckwith-Wiedemann Syndrome/diagnostic imaging , Cysts/diagnostic imaging , Hemorrhage/diagnostic imaging , Adrenal Gland Diseases/complications , Beckwith-Wiedemann Syndrome/complications , Cysts/complications , Female , Hemorrhage/complications , Humans , Infant, Newborn , Radiography
16.
Braz. j. infect. dis ; 7(6): 429-432, dez. 2003. ilus
Article in English | LILACS | ID: lil-357658

ABSTRACT

Citrobacter, a Gram-negative enteric bacillus, is a rare cause of septicemia and meningitis, seldom reported beyond the neonatal period. It is characterized by a fulminant clinical course and a high incidence of complications, including brain abscesses. We studied a three-month-old infant with Citrobacter meningitis, who developed acute communicating hydrocephalus and multiple periventricular brain abscesses while on treatment. The patient died, despite intensive antibiotic treatment directed towards the causative organism, C. diversus.


Subject(s)
Humans , Infant , Male , Brain Abscess , Citrobacter , Enterobacteriaceae Infections , Meningitis, Bacterial , Brain Abscess , Enterobacteriaceae Infections , Fatal Outcome , Meningitis, Bacterial
17.
Braz J Infect Dis ; 7(6): 429-32, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14636485

ABSTRACT

Citrobacter, a Gram-negative enteric bacillus, is a rare cause of septicemia and meningitis, seldom reported beyond the neonatal period. It is characterized by a fulminant clinical course and a high incidence of complications, including brain abscesses. We studied a three-month-old infant with Citrobacter meningitis, who developed acute communicating hydrocephalus and multiple periventricular brain abscesses while on treatment. The patient died, despite intensive antibiotic treatment directed towards the causative organism, C. diversus.


Subject(s)
Brain Abscess/microbiology , Citrobacter/isolation & purification , Enterobacteriaceae Infections/microbiology , Meningitis, Bacterial/microbiology , Brain Abscess/drug therapy , Enterobacteriaceae Infections/drug therapy , Fatal Outcome , Humans , Infant , Male , Meningitis, Bacterial/drug therapy
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