Radiological work-up in Peutz-Jeghers syndrome

被引:20
作者
Kurugoglu, S [1 ]
Aksoy, H [1 ]
Kantarci, F [1 ]
Cetinkaya, S [1 ]
Mihmanli, I [1 ]
Korman, U [1 ]
机构
[1] Univ Istanbul, Cerrahpasa Med Fac, Dept Radiol, TR-34300 Istanbul, Turkey
关键词
gastrointestinal stomach; small bowel; Peutz-Jeghers syndrome; enteroclysis;
D O I
10.1007/s00247-003-1031-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background. The development of modern imaging studies such as high-resolution US and various MR imaging sequences have enabled their application to the examination of the gastrointestinal tract. Objective. To compare radiological contrast studies, US and MRI in patients with Peutz-Jeghers syndrome (PJS). Materials and methods. Ten members of two families were evaluated. The patients were divided into three groups according to the presence of perioral pigmentations and current clinical symptomatology. Patients were examined using US, MRI and radiological contrast studies. Results. In the disease-free family members (n=3), no pathological findings were found. In asymptomatic (n=4) and symptomatic patients (n=3), polyps were demonstrated using contrast studies in all cases. MRI demonstrated all the polyps. Ultrasound revealed the polyps in three out of six patients. In addition to the polyps, intussusceptions were shown. There was no evidence of malignant transformation on any of the studies. Conclusions. Although PJS is a childhood or teenage disease, patients should be closely monitored during adulthood because of the development of gastrointestinal and extragastrointestinal malignancies. Contrast studies remain the gold standard. However, radiological follow-up could be undertaken by US or MRI, which would not impose a radiation burden during life-time follow-up.
引用
收藏
页码:766 / 771
页数:6
相关论文
共 15 条
[1]   Increased risk for cancer in patients with the Peutz-Jeghers syndrome [J].
Boardman, LA ;
Thibodeau, SN ;
Schaid, DJ ;
Lindor, NM ;
McDonnell, SK ;
Burgart, LJ ;
Ahlquist, DA ;
Podratz, KC ;
Pittelkow, M ;
Hartmann, LC .
ANNALS OF INTERNAL MEDICINE, 1998, 128 (11) :896-+
[2]   PEUTZ-JEGHERS SYNDROME [J].
BUCK, JL ;
HARNED, RK ;
LICHTENSTEIN, JE ;
SOBIN, LH .
RADIOGRAPHICS, 1992, 12 (02) :365-378
[3]   GASTROINTESTINAL POLYPOSIS SYNDROMES [J].
FINAN, MC ;
RAY, MK .
DERMATOLOGIC CLINICS, 1989, 7 (03) :419-434
[4]   INCREASED RISK OF CANCER IN THE PEUTZ-JEGHERS SYNDROME [J].
GIARDIELLO, FM ;
WELSH, SB ;
HAMILTON, SR ;
OFFERHAUS, GJA ;
GITTELSOHN, AM ;
BOOKER, SV ;
KRUSH, AJ ;
YARDLEY, JH ;
LUK, GD .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (24) :1511-1514
[5]   THE HAMARTOMATOUS POLYPOSIS SYNDROMES - CLINICAL AND RADIOLOGIC FEATURES [J].
HARNED, RK ;
BUCK, JL ;
SOBIN, LH .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1995, 164 (03) :565-571
[6]   Sonographic diagnosis of multiple small-bowel intussusceptions in Peutz-Jeghers syndrome: a case report [J].
Harris, JP ;
Munden, MM ;
Minifee, PK .
PEDIATRIC RADIOLOGY, 2002, 32 (09) :681-683
[7]  
Izzidien A Y, 2002, Surg Endosc, V16, P715
[8]   Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase [J].
Jenne, DE ;
Reimann, H ;
Nezu, J ;
Friedel, W ;
Loff, S ;
Jeschke, R ;
Müller, D ;
Back, W ;
Zimmer, M .
NATURE GENETICS, 1998, 18 (01) :38-44
[9]   Peutz-Jeghers Syndrome -: recent developments of non-invasive diagnostic procedures. [J].
Köppelmann, S ;
Lörcher, U ;
Keller, KM ;
Weitzel, D .
KLINISCHE PADIATRIE, 2000, 212 (06) :332-335
[10]   MR imaging of the small bowel using the HASTE sequence [J].
Lee, JKT ;
Marcos, HB ;
Semelka, RC .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1998, 170 (06) :1457-1463