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  • 1
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    London : Periodicals Archive Online (PAO)
    Journal of adolescence. 17:2 (1994) 137 
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  • 2
    ISSN: 1432-1076
    Keywords: Atypical mycobacteria ; Gamma interferon ; Non-tuberculous mycobacterial lymphadenitis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Infection withMycobacterium avium, M. intracellulare and M. scrofulaceum (MAIS) organisms in normal children may result in cervical lymphadenopathy. There is a poor response to anti-tuberculous therapy and surgical excision of infected nodes is necessary. The diagnosis therefore requires consideration in children with cervical lymphadenopathy. A simple in vitro assay is described which may be useful for diagnosis prior to excision. Whole blood is cultured withM. avium purified protein derivative. After 24h the plasma is removed and the concentration of gamma interferon (IFN-γ) quantified by a radioimmunometric assay. In a prospective study of 38 children with neck lesions, 16 showed MAIS organisms isolated from cultures of excised tissue. The level of IFN-γ produced by peripheral blood lymphocytes from children in the MAIS group was significantly greater when compared with children having operations for neck lesions that were not due to MAIS organisms (P〈0.001).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 7 (1992), S. 165-170 
    ISSN: 1437-9813
    Keywords: Crohn's disease ; Childhood ; Bowel resection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract During the years 1979–1988, 63 children (38 male: 25 female) were first diagnosed as having Crohn's disease on the basis of histological findings. Twenty-nine per cent were less than 10 years old at the onset of symptoms; 40% of these cases took more than 1 year to diagnose. Most patients (59%) presented with abdominal pain and diarrhoea, but 40% presented with: a non-specific illness (14%); upper gastro-intestinal tract symptoms (14%); growth failure (6%); systemic disease (5%), or peri-anal disease (1%). There were signs of abdominal tenderness, distension, or an abdominal mass in over 50% of cases. Peri-anal Crohn's disease was present in 41% and a height less than the 10th centile was recorded at diagnosis in 45%. Children were treated with a combination of prednisolone and sulphasalazine. In 16 cases a bowel resection was performed. Surgery was indicated for localised stricture formation causing obstruction and for persistence of severe disease poorly responsive to steroids, particularly in the prepubertal child with growth failure. The extent and distribution of disease influenced outcome. Twenty-four of 39 children followed for more than 3 years are either well-controlled or disease-free at present.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1437-9813
    Keywords: Persistent müllerian duct syndrome ; Müllerian inhibiting substance ; Gubernaculum ; Testicular descent
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A 4-month-old phenotypic male with persistent müllerian duct syndrome (PMDS) is described. Serum levels of müllerian inhibiting substance (MIS) were undetectable in an enzyme immunoassay, consistent with a in an MIS gene. Normal germ cells were present in the testis, suggesting that subsequent azoospermia found in other patients with this abnormality is caused by a postnatal defect in germ cell development after 4 months of age. The testes were not attached by normal male gubernacula, but were loosely anchored by a long “round ligament” to the inguinal region. Failure of masculinasation of the gubernaculum in this syndrome suggests that MIS is responsible for early gubernacular development, and hence may have a role in testicular descent.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 7 (1992), S. 253-255 
    ISSN: 1437-9813
    Keywords: Paediatric ; Cystic hygroma ; Lymphangioma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Cystic hygromas (benign tumours of the lymphatic system or lymphangiomas) occur predominantly in the head and neck region of infants and children. They can be grouped into three prognostic categories: (1) simple cystic hygroma; (2) cystic hygroma with oropharyngeal involvement; and (3) cystic hygroma with mediastinal involvement. At the Royal Children's Hospital, Melbourne, during a 16 year period (1973–1988) 47 of 122 (39%) patients admitted with a lymphangioma were classified as cervical cystic hygroma. Simple cystic hygromas, presenting as a lump, occurred in 33 children. In 28, uncomplicated excision was possible. Nine children presented at birth with cystic hygroma with oro-pharyngeal involvement, 5 of whom had severe respiratory distress. All 9 required multiple excisions; death occurred in 1. Cervicomediastinal cystic hygroma occurred in 5 children presenting between birth and 2 years. Mediastinal involvement was confirmed by chest X-ray. All children had thoracocervical excision without early complications; 2 had cervical recurrence.
    Type of Medium: Electronic Resource
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