Only two cases of coexisting von Recklinghausen's disease and neuroblastoma have been reported in the English literature, and in both the diagnosis of neurofibromatosis is somewhat tenuous. We report the case of a child with disseminated neuroblastoma who had a previous unequivocal diagnosis of von
Massive plexiform neurofibroma in the orbit in a child with von Recklinghausen's disease
β Scribed by M. Tada; Yutaka Sawamura; Nobuaki Ishii; Shinki Chin; Hiroshi Abe
- Publisher
- Springer
- Year
- 1998
- Tongue
- English
- Weight
- 786 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0256-7040
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π SIMILAR VOLUMES
A five-and-one-half-year-old boy, referred for orthopaedic evaluation of spinal curvature, was diagnosed as having neurofibromatosis (von Recklinghausen's disease) with a 44-degree right thoracolumbar curve from T-10 to L-3 A soft-tissue mass was identified in the area of T-7 to T-12 and, when neuro
The effect of serum from patients with yon Recklinghausen's disease [neurofibromatosis (NF)] on the cell growth and DNA synthesis of cultured neurofibroma-derived cells (NF fibroblasts grown from explant cultures of cutaneous neurofibromas from seven NF patients, and Schwann cells from a single-cell
## Abstract A young child with neurofibromatosis type 1 (NF1) is reported who developed two primary malignancies: a glioblastoma, followed 6 months later by an abdominal B cell nonβHodgkin's lymphoma. The child is now 4.5 years off treatment and disease free, but has developed progressive and sever