Journal of obstetrics and gynaecology (Tokyo, Japan) · 1995
Magnetic resonance imaging of autosomal recessive polycystic kidney disease in utero.
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Nishi T
Аннотация
OBJECTIVE: To assess the efficacy of ultrasonography (USG) and magnetic resonance imaging (MRI) in diagnosing a particular urologic disease, autosomal recessive polycystic kidney disease (ARPKD).
SUBJECT: A patient with a case of ARPKD, as diagnosed by USG and MRI.
RESULT: USG revealed features typical of ARPKD; the kidneys were enlarged and echogenic, with a loss of normal renal architecture. MRI revealed anatomical features similar to those demonstrated by USG. Furthermore, MRI showed clearer delineation and tissue specificity of the affected kidneys.
CONCLUSION: USG and MRI were useful in diagnosing ARPKD. MRI can serve as an adjunctive method for diagnosing certain fetal anomalies.
SUBJECT: A patient with a case of ARPKD, as diagnosed by USG and MRI.
RESULT: USG revealed features typical of ARPKD; the kidneys were enlarged and echogenic, with a loss of normal renal architecture. MRI revealed anatomical features similar to those demonstrated by USG. Furthermore, MRI showed clearer delineation and tissue specificity of the affected kidneys.
CONCLUSION: USG and MRI were useful in diagnosing ARPKD. MRI can serve as an adjunctive method for diagnosing certain fetal anomalies.