A case of fetal osteogenesis imperfecta type 2A: longitudinal observation of natural course in utero and pitfalls for prenatal ultrasound diagnosis

被引:1
|
作者
Kimura, Ibuki [1 ]
Araki, Ryota [1 ]
Yoshizato, Toshiyuki [2 ]
Miyamoto, Shingo [1 ]
机构
[1] Fukuoka Univ, Fac Med, Dept Obstet & Gynecol, Fukuoka 8140180, Japan
[2] Fukuoka Univ Hosp, Ctr Maternal Fetal & Neonatal Med, Jonan Ku, Fukuoka 8140180, Japan
关键词
Osteogenesis imperfecta type 2A; Ultrasonography; Prenatal diagnosis; INCREASED NUCHAL TRANSLUCENCY; SKELETAL DYSPLASIAS; 1ST-TRIMESTER DIAGNOSIS; SONOGRAPHIC DIAGNOSIS; PULMONARY HYPOPLASIA; ASSOCIATION; TRIMESTER; SIGN;
D O I
10.1007/s10396-015-0645-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
We present a case of osteogenesis imperfecta (OI) type 2A in which a natural course in utero was observed from 23 weeks' gestation to term. At 23 weeks' gestation, a sonographic examination showed a cloverleaf skull-like head, a narrow thorax, and marked shortening of the long bones with bowing of the femurs and humeri. Follow-up examinations showed that the cloverleaf skull-like head was not evident at 28 weeks' gestation. Discontinuity of the ribs and femurs was observed at 26 and 30 weeks' gestation, respectively. This finding suggested bone fractures, which were confirmed by three-dimensional computed tomography at 32 weeks' gestation. Ultrasonographic findings of bones, including the long bones and calvarium, changed with advancing gestation during the second trimester. Characteristic features of OI type 2A were evident during the late second to early third trimesters. Repeated ultrasonographic examinations together with three-dimensional computed tomography are necessary for the definitive diagnosis of OI type 2A in the second trimester.
引用
收藏
页码:565 / 570
页数:6
相关论文
共 19 条
  • [1] A case of fetal osteogenesis imperfecta type 2A: longitudinal observation of natural course in utero and pitfalls for prenatal ultrasound diagnosis
    Ibuki Kimura
    Ryota Araki
    Toshiyuki Yoshizato
    Shingo Miyamoto
    Journal of Medical Ultrasonics, 2015, 42 : 565 - 570
  • [2] Prenatal diagnosis of osteogenesis imperfecta type 2: case report
    dos Santos, Caroline Mombaque
    Pancich Gallarreta, Francisco Maximiliano
    dos Santos, Wendel Mombaque
    Schroer, Caroline Eckerdt
    de Morais, Edson Nunes
    SCIENTIA MEDICA, 2015, 25 (01)
  • [3] Osteogenesis imperfecta type 2: A fetal case report
    不详
    VIRCHOWS ARCHIV, 2005, 447 (02) : 277 - 278
  • [4] Prenatal diagnosis of osteogenesis imperfecta type 3 and 4: A case report
    Kartal, E.
    Pakay, K.
    Akkurt, M.
    EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2022, 270 : E7 - E8
  • [5] PRENATAL-DIAGNOSIS OF OSTEOGENESIS IMPERFECTA TYPE-II BY REAL-TIME ULTRASOUND
    STEPHENS, JD
    FILLY, RA
    CALLEN, PW
    GOLBUS, MS
    HUMAN GENETICS, 1983, 64 (02) : 191 - 193
  • [6] Prenatal diagnosis of osteogenesis imperfecta type II by three-dimensional ultrasound and computed tomography
    Suzumori, Nobuhiro
    Hasegawa, Tomonobu
    Sugiura-Ogasawara, Mayumi
    JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2011, 37 (06) : 664 - 665
  • [7] PRENATAL-DIAGNOSIS OF OSTEOGENESIS IMPERFECTA (REPORT ON A CASE ATTRIBUTED TO THE CLASSICAL EKMAN LOBSTEIN TYPE)
    CHALUBINSKI, K
    SCHALLER, A
    ULTRASCHALL IN DER MEDIZIN, 1994, 15 (01): : 38 - 42
  • [8] ANALYSIS OF CULTURED CHORIONIC VILLI IN A CASE OF OSTEOGENESIS IMPERFECTA TYPE-II - IMPLICATIONS FOR PRENATAL-DIAGNOSIS
    GRANGE, DK
    LEWIS, MB
    MARINI, JC
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 36 (02): : 258 - 264
  • [9] Initial experience using magnetic resonance imaging in prenatal diagnosis of osteogenesis imperfecta type II - A case report
    Teng, SW
    Guo, WY
    Sheu, MH
    Wang, PH
    CLINICAL IMAGING, 2003, 27 (01) : 55 - 58
  • [10] ANTENATAL DIAGNOSIS OF OSTEOGENESIS IMPERFECTA BY REAL-TIME ULTRASOUND - 2 CASE-REPORTS
    MILSOM, I
    MATTSSON, LA
    DAHLENNILSSON, I
    BRITISH JOURNAL OF RADIOLOGY, 1982, 55 (652): : 310 - 312