Your browser doesn't support javascript.
loading
Diagnosis and whole body screening using blood pool scintigraphy for evaluating congenital vascular malformations.
Kim, Young Hwan; Choi, Joon Young; Kim, Young-Wook; Kim, Dong-Ik; Do, Young Soo; Choe, Yearn Seong; Lee, Kyung-Han; Kim, Byung-Tae.
Affiliation
  • Kim YH; Department of Nuclear Medicine, Hanyang University Guri Hospital, Hanyang University School of Medicine, Guri-si, Gyeonggi-do, Korea; Department of Nuclear Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Choi JY; Department of Nuclear Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. Electronic address: jynm.choi@samsung.com.
  • Kim YW; Division of Vascular Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Kim DI; Division of Vascular Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Do YS; Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Choe YS; Department of Nuclear Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Lee KH; Department of Nuclear Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Kim BT; Department of Nuclear Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Ann Vasc Surg ; 28(3): 673-8, 2014 Apr.
Article in En | MEDLINE | ID: mdl-24295885
ABSTRACT

BACKGROUND:

Because magnetic resonance imaging and angiography are inappropriate for whole-body screening because of high cost or invasiveness, we investigated the potential of whole-body blood pool scintigraphy (WBBPS) as a screening and diagnostic tool for congenital vascular malformations (CVMs).

METHODS:

The subjects of the study were 137 patients (mean age 20 ± 16 years; range 0.3-68 years) with suspected CVM. Whole-body anterior and posterior images were acquired twenty minutes after injection of 760 MBq (99m)Tc-labeled red blood cells (pediatric dose 13 MBq/kg). The final diagnosis was determined by clinical findings, magnetic resonance imaging, angiography, Doppler sonography, and lymphoscintigraphy.

RESULTS:

Of these patients, 124 had venous malformations, and 13 had lymphatic malformations. WBBPS successfully detected abnormal blood pooling lesions in 96.8% (120/124) of the patients with venous malformations. None of the patients with lymphatic malformation showed abnormal uptake on WBBPS. In addition, WBBPS detected 41 additional abnormal vascular lesions that were not found during initial clinical evaluation in 16.9% (21/124) of the patients with venous malformations.

CONCLUSION:

WBBPS is a valuable diagnostic and screening modality for the initial evaluation of CVM because of its high characterizing accuracy of 97.1% and the ability to image the whole body.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Gated Blood-Pool Imaging / Whole Body Imaging / Vascular Malformations / Lymphoscintigraphy / Lymphatic Diseases Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies / Screening_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Year: 2014 Type: Article

Full text: 1 Database: MEDLINE Main subject: Gated Blood-Pool Imaging / Whole Body Imaging / Vascular Malformations / Lymphoscintigraphy / Lymphatic Diseases Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies / Screening_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Year: 2014 Type: Article