A Meckel's diverticulum containing pancreatic tissue and nesidioblastosis in a patient with Beckwith-Wiedemann syndrome
✍ Scribed by F. Schier; A. Sauerbrey; H. Kosmehl
- Publisher
- Springer-Verlag
- Year
- 2000
- Tongue
- English
- Weight
- 305 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0179-0358
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Beckwith–Wiedemann syndrome (BWS) is a genetic disorder associated with an increased risk of childhood tumors. Here we describe a patient with BWS who developed a central nervous system atypical teratoid/rhabdoid tumor (AT/RT). To our knowledge, despite the known cancer predisposition,
## Abstract To evaluate the usefulness of regular radiographic screening to detect an asymptomatic intraabdominal tumor in patients with an increased risk of developing Wilms tumor, we reviewed the files of patients with hemihypertrophy, aniridia, or Beckwith‐Wiedemann syndrome who were registered